Drakulić, Dunja

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Authority KeyName Variants
f5a3c9c9-c871-4d31-97e0-bc1c420a3d20
  • Drakulić, Dunja (8)
  • Drakulić, Dunja R (3)
  • Drakulić, Dunja R. (1)
Projects
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200007 (University of Belgrade, Institute for Biological Research 'Siniša Stanković') Cellular and molecular basis of neuroinflamation: potential targets for translational medicine and therapy
Molecular mechanisms of cellular responses on pathological changes in central neuronal system and peripheral organs of mammals Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200017 (University of Belgrade, Institute of Nuclear Sciences 'Vinča', Belgrade-Vinča)
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200178 (University of Belgrade, Faculty of Biology) Design, synthesis and investigations of fullerene based nanomolecular machines
Bioactive natural products as potential sources of new pharmaceuticals and food supplements Molecular mechanisms of redox signalling in homeostasis: adaptation and pathology
Signaling molecules in diabetes: search for potential targets in intrinsic pathways for prediction and intervention in diabetes Effects of metabolic and nonmetabolic stressors on the expression and action of neuroendocrine regulators of energy homeostasis
Ministry of Education, Science and Technological Development, Republic of Serbia, Grant no. 451-03-68/2020-14/200175 (Institute of Technical Sciences of SASA, Belgrade) Cellular and molecular basis of malignant and cardiovascular diseases-clinical implications
V.I.R.U.S. – Survivors of COVID19: variety of immune responses to SARS-CoV-2 in correlation with clinical manifestation. Long term follow up The Ministry of Education, Science and Technological Development, grants No 451-03-1/2022-14/13

Author's Bibliography

Serum High-Mobility Group Box 1 and Heme Oxygenase 1 as Biomarkers in COVID-19 Patients at Hospital Admission

Grigorov, Ilijana; Pejić, Snežana; Todorović, Ana; Drakulić, Dunja; Veljković, Filip; Miletić-Vukajlović, Jadranka; Bobić, Katarina; Soldatović, Ivan; Đurašević, Siniša; Jasnić, Nebojša; Stanković, Sanja; Glumac, Sofija; Mihailović-Vučinić, Violeta; Milenković, Branislava

(Basel: MDPI, 2023)

TY  - JOUR
AU  - Grigorov, Ilijana
AU  - Pejić, Snežana
AU  - Todorović, Ana
AU  - Drakulić, Dunja
AU  - Veljković, Filip
AU  - Miletić-Vukajlović, Jadranka
AU  - Bobić, Katarina
AU  - Soldatović, Ivan
AU  - Đurašević, Siniša
AU  - Jasnić, Nebojša
AU  - Stanković, Sanja
AU  - Glumac, Sofija
AU  - Mihailović-Vučinić, Violeta
AU  - Milenković, Branislava
PY  - 2023
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/6126
AB  - The careful monitoring of patients with mild/moderate COVID-19 is of particular importance because of the rapid progression of complications associated with COVID-19. For prognostic reasons and for the economic management of health care resources, additional biomarkers need to be identified, and their monitoring can conceivably be performed in the early stages of the disease. In this retrospective cross-sectional study, we found that serum concentrations of high-mobility group box 1 (HMGB1) and heme oxygenase-1 (HO-1), at the time of hospital admission, could be useful biomarkers for COVID-19 management. The study included 160 randomly selected recovered patients with mild to moderate COVID-19 on admission. Compared with healthy controls, serum HMGB1 and HO-1 levels increased by 487.6 pg/mL versus 43.1 pg/mL and 1497.7 pg/mL versus 756.1 pg/mL, respectively. Serum HO-1 correlated significantly with serum HMGB1, oxidative stress parameters (malondialdehyde (MDA), the phosphatidylcholine/lysophosphatidylcholine ratio (PC/LPC), the ratio of reduced and oxidative glutathione (GSH/GSSG)), and anti-inflammatory acute phase proteins (ferritin, haptoglobin). Increased heme catabolism/hemolysis were not detected. We hypothesize that the increase in HO-1 in the early phase of COVID-19 disease is likely to have a survival benefit by providing protection against oxidative stress and inflammation, whereas the level of HMGB1 increase reflects the activity of the innate immune system and represents levels within which the disease can be kept under control.
PB  - Basel: MDPI
T2  - International Journal of Molecular Sciences
T1  - Serum High-Mobility Group Box 1 and Heme Oxygenase 1 as Biomarkers in COVID-19 Patients at Hospital Admission
IS  - 17
VL  - 24
DO  - 10.3390/ijms241713164
SP  - 13164
ER  - 
@article{
author = "Grigorov, Ilijana and Pejić, Snežana and Todorović, Ana and Drakulić, Dunja and Veljković, Filip and Miletić-Vukajlović, Jadranka and Bobić, Katarina and Soldatović, Ivan and Đurašević, Siniša and Jasnić, Nebojša and Stanković, Sanja and Glumac, Sofija and Mihailović-Vučinić, Violeta and Milenković, Branislava",
year = "2023",
abstract = "The careful monitoring of patients with mild/moderate COVID-19 is of particular importance because of the rapid progression of complications associated with COVID-19. For prognostic reasons and for the economic management of health care resources, additional biomarkers need to be identified, and their monitoring can conceivably be performed in the early stages of the disease. In this retrospective cross-sectional study, we found that serum concentrations of high-mobility group box 1 (HMGB1) and heme oxygenase-1 (HO-1), at the time of hospital admission, could be useful biomarkers for COVID-19 management. The study included 160 randomly selected recovered patients with mild to moderate COVID-19 on admission. Compared with healthy controls, serum HMGB1 and HO-1 levels increased by 487.6 pg/mL versus 43.1 pg/mL and 1497.7 pg/mL versus 756.1 pg/mL, respectively. Serum HO-1 correlated significantly with serum HMGB1, oxidative stress parameters (malondialdehyde (MDA), the phosphatidylcholine/lysophosphatidylcholine ratio (PC/LPC), the ratio of reduced and oxidative glutathione (GSH/GSSG)), and anti-inflammatory acute phase proteins (ferritin, haptoglobin). Increased heme catabolism/hemolysis were not detected. We hypothesize that the increase in HO-1 in the early phase of COVID-19 disease is likely to have a survival benefit by providing protection against oxidative stress and inflammation, whereas the level of HMGB1 increase reflects the activity of the innate immune system and represents levels within which the disease can be kept under control.",
publisher = "Basel: MDPI",
journal = "International Journal of Molecular Sciences",
title = "Serum High-Mobility Group Box 1 and Heme Oxygenase 1 as Biomarkers in COVID-19 Patients at Hospital Admission",
number = "17",
volume = "24",
doi = "10.3390/ijms241713164",
pages = "13164"
}
Grigorov, I., Pejić, S., Todorović, A., Drakulić, D., Veljković, F., Miletić-Vukajlović, J., Bobić, K., Soldatović, I., Đurašević, S., Jasnić, N., Stanković, S., Glumac, S., Mihailović-Vučinić, V.,& Milenković, B.. (2023). Serum High-Mobility Group Box 1 and Heme Oxygenase 1 as Biomarkers in COVID-19 Patients at Hospital Admission. in International Journal of Molecular Sciences
Basel: MDPI., 24(17), 13164.
https://doi.org/10.3390/ijms241713164
Grigorov I, Pejić S, Todorović A, Drakulić D, Veljković F, Miletić-Vukajlović J, Bobić K, Soldatović I, Đurašević S, Jasnić N, Stanković S, Glumac S, Mihailović-Vučinić V, Milenković B. Serum High-Mobility Group Box 1 and Heme Oxygenase 1 as Biomarkers in COVID-19 Patients at Hospital Admission. in International Journal of Molecular Sciences. 2023;24(17):13164.
doi:10.3390/ijms241713164 .
Grigorov, Ilijana, Pejić, Snežana, Todorović, Ana, Drakulić, Dunja, Veljković, Filip, Miletić-Vukajlović, Jadranka, Bobić, Katarina, Soldatović, Ivan, Đurašević, Siniša, Jasnić, Nebojša, Stanković, Sanja, Glumac, Sofija, Mihailović-Vučinić, Violeta, Milenković, Branislava, "Serum High-Mobility Group Box 1 and Heme Oxygenase 1 as Biomarkers in COVID-19 Patients at Hospital Admission" in International Journal of Molecular Sciences, 24, no. 17 (2023):13164,
https://doi.org/10.3390/ijms241713164 . .
1
1

Efekti pretretmana meldonijumom na tokove različitih modela sepsi kod pacova

Lakić, Iva; Đurašević, Siniša; Ružičić, Aleksandra; Tosti, Tomislav; Đurović, Saša; Glumac, Sofija; Pavlović, Slađan; Borković-Mitić, Slavica; Grigorov, Ilijana; Stanković, Sanja; Pejić, Snežana; Todorović, Ana; Drakulić, Dunja; Jasnić, Nebojša; Đorđević, Jelena; Todorović, Zoran

(Belgrade: Serbian Biological Society, 2022)

TY  - CONF
AU  - Lakić, Iva
AU  - Đurašević, Siniša
AU  - Ružičić, Aleksandra
AU  - Tosti, Tomislav
AU  - Đurović, Saša
AU  - Glumac, Sofija
AU  - Pavlović, Slađan
AU  - Borković-Mitić, Slavica
AU  - Grigorov, Ilijana
AU  - Stanković, Sanja
AU  - Pejić, Snežana
AU  - Todorović, Ana
AU  - Drakulić, Dunja
AU  - Jasnić, Nebojša
AU  - Đorđević, Jelena
AU  - Todorović, Zoran
PY  - 2022
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/5933
AB  - Сепса је стање опасно по живот узроковано нерегулисаним и прекомерним
одговором на инфекцију, које праћено инфламацијом и поремећеним
метаболизмом липида доводи до постепеног отказивања органа.1,2 Мелдонијум је
антиинфламаторни лек који се користи за лечење исхемије миокарда.3 Он делује
тако што преусмерава производњу енергије са оксидације масних киселина на
гликолизу, као пут који троши мање кисеоника. На овај начин мелдонијум
негативно утиче на метаболизам липида. Истраживали смо ефекте
четворонедељног претретмана мелдонијумом на ток фекалне сепсе (ФИП) и сепсе
изазиване липополисахаридом (ЛПС), код мужјака пацова. Изненађујуће, у
условима фекалне сепсе, мелдонијум је повећао стопу морталитета животиња у
поређењу са групом која није третирана мелдонијумом. Анализе оксидативног и
инфламаторног статуса ткива (срце, јетра, бубрези) потврдиле су
антиинфламаторне, антиапоптотске и антинекротичке ефекте мелдонијума, код оба
модела сепсе. Када је реч о производњи енергије, упркос неким сличностима,
утврђене су разлике у ова два модела. Једна од очигледних разлика је у одговору
симпатоадреналног система, који је изостао код ФИП модела, док је код ЛПС
модела довео до двоструког повећања концентрације катехоламина у серуму. Ова
студија показује важност ненарушене производње енергије скрећући пажњу на
потребу ревизије постојећих смерница у клиничком лечењу сепсе, али и отвара пут
за откривање нових терапијских приступа.
AB  - Sepsa je stanje opasno po život uzrokovano neregulisanim i prekomernim odgovorom na infekciju, koje praćeno inflamacijom i poremećenim metabolizmom lipida dovodi do postepenog otkazivanja organa.1,2 Meldonijum je antiinflamatorni lek koji se koristi za lečenje ishemije miokarda.3 On deluje tako što preusmerava proizvodnju energije sa oksidacije masnih kiselina na glikolizu, kao put koji troši manje kiseonika. Na ovaj način meldonijum negativno utiče na metabolizam lipida. Istraživali smo efekte četvoronedeljnog pretretmana meldonijumom na tok fekalne sepse (FIP) i sepse izazivane lipopolisaharidom (LPS), kod mužjaka pacova. Iznenađujuće, u uslovima fekalne sepse, meldonijum je povećao stopu mortaliteta životinja u poređenju sa grupom koja nije tretirana meldonijumom. Analize oksidativnog i inflamatornog statusa tkiva (srce, jetra, bubrezi) potvrdile su antiinflamatorne, antiapoptotske i antinekrotičke efekte meldonijuma, kod oba modela sepse. Kada je reč o proizvodnji energije, uprkos nekim sličnostima, utvrđene su razlike u ova dva modela. Jedna od očiglednih razlika je u odgovoru simpatoadrenalnog sistema, koji je izostao kod FIP modela, dok je kod LPS modela doveo do dvostrukog povećanja koncentracije kateholamina u serumu. Ova studija pokazuje važnost nenarušene proizvodnje energije skrećući pažnju na potrebu revizije postojećih smernica u kliničkom lečenju sepse, ali i otvara put za otkrivanje novih terapijskih pristupa.
PB  - Belgrade: Serbian Biological Society
C3  - Knjiga sažetaka: Treći Kongres biologa Srbije: Osnovna i primenjena istraživanja: Metodika nastave; 2022 Sep 21-25; Zlatibor, Serbia
T1  - Efekti pretretmana meldonijumom na tokove različitih modela sepsi kod pacova
T1  - Ефекти претретмана мелдонијумом на токове различитих модела сепси код пацова
SP  - 340
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_5933
ER  - 
@conference{
author = "Lakić, Iva and Đurašević, Siniša and Ružičić, Aleksandra and Tosti, Tomislav and Đurović, Saša and Glumac, Sofija and Pavlović, Slađan and Borković-Mitić, Slavica and Grigorov, Ilijana and Stanković, Sanja and Pejić, Snežana and Todorović, Ana and Drakulić, Dunja and Jasnić, Nebojša and Đorđević, Jelena and Todorović, Zoran",
year = "2022",
abstract = "Сепса је стање опасно по живот узроковано нерегулисаним и прекомерним
одговором на инфекцију, које праћено инфламацијом и поремећеним
метаболизмом липида доводи до постепеног отказивања органа.1,2 Мелдонијум је
антиинфламаторни лек који се користи за лечење исхемије миокарда.3 Он делује
тако што преусмерава производњу енергије са оксидације масних киселина на
гликолизу, као пут који троши мање кисеоника. На овај начин мелдонијум
негативно утиче на метаболизам липида. Истраживали смо ефекте
четворонедељног претретмана мелдонијумом на ток фекалне сепсе (ФИП) и сепсе
изазиване липополисахаридом (ЛПС), код мужјака пацова. Изненађујуће, у
условима фекалне сепсе, мелдонијум је повећао стопу морталитета животиња у
поређењу са групом која није третирана мелдонијумом. Анализе оксидативног и
инфламаторног статуса ткива (срце, јетра, бубрези) потврдиле су
антиинфламаторне, антиапоптотске и антинекротичке ефекте мелдонијума, код оба
модела сепсе. Када је реч о производњи енергије, упркос неким сличностима,
утврђене су разлике у ова два модела. Једна од очигледних разлика је у одговору
симпатоадреналног система, који је изостао код ФИП модела, док је код ЛПС
модела довео до двоструког повећања концентрације катехоламина у серуму. Ова
студија показује важност ненарушене производње енергије скрећући пажњу на
потребу ревизије постојећих смерница у клиничком лечењу сепсе, али и отвара пут
за откривање нових терапијских приступа., Sepsa je stanje opasno po život uzrokovano neregulisanim i prekomernim odgovorom na infekciju, koje praćeno inflamacijom i poremećenim metabolizmom lipida dovodi do postepenog otkazivanja organa.1,2 Meldonijum je antiinflamatorni lek koji se koristi za lečenje ishemije miokarda.3 On deluje tako što preusmerava proizvodnju energije sa oksidacije masnih kiselina na glikolizu, kao put koji troši manje kiseonika. Na ovaj način meldonijum negativno utiče na metabolizam lipida. Istraživali smo efekte četvoronedeljnog pretretmana meldonijumom na tok fekalne sepse (FIP) i sepse izazivane lipopolisaharidom (LPS), kod mužjaka pacova. Iznenađujuće, u uslovima fekalne sepse, meldonijum je povećao stopu mortaliteta životinja u poređenju sa grupom koja nije tretirana meldonijumom. Analize oksidativnog i inflamatornog statusa tkiva (srce, jetra, bubrezi) potvrdile su antiinflamatorne, antiapoptotske i antinekrotičke efekte meldonijuma, kod oba modela sepse. Kada je reč o proizvodnji energije, uprkos nekim sličnostima, utvrđene su razlike u ova dva modela. Jedna od očiglednih razlika je u odgovoru simpatoadrenalnog sistema, koji je izostao kod FIP modela, dok je kod LPS modela doveo do dvostrukog povećanja koncentracije kateholamina u serumu. Ova studija pokazuje važnost nenarušene proizvodnje energije skrećući pažnju na potrebu revizije postojećih smernica u kliničkom lečenju sepse, ali i otvara put za otkrivanje novih terapijskih pristupa.",
publisher = "Belgrade: Serbian Biological Society",
journal = "Knjiga sažetaka: Treći Kongres biologa Srbije: Osnovna i primenjena istraživanja: Metodika nastave; 2022 Sep 21-25; Zlatibor, Serbia",
title = "Efekti pretretmana meldonijumom na tokove različitih modela sepsi kod pacova, Ефекти претретмана мелдонијумом на токове различитих модела сепси код пацова",
pages = "340",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_5933"
}
Lakić, I., Đurašević, S., Ružičić, A., Tosti, T., Đurović, S., Glumac, S., Pavlović, S., Borković-Mitić, S., Grigorov, I., Stanković, S., Pejić, S., Todorović, A., Drakulić, D., Jasnić, N., Đorđević, J.,& Todorović, Z.. (2022). Efekti pretretmana meldonijumom na tokove različitih modela sepsi kod pacova. in Knjiga sažetaka: Treći Kongres biologa Srbije: Osnovna i primenjena istraživanja: Metodika nastave; 2022 Sep 21-25; Zlatibor, Serbia
Belgrade: Serbian Biological Society., 340.
https://hdl.handle.net/21.15107/rcub_ibiss_5933
Lakić I, Đurašević S, Ružičić A, Tosti T, Đurović S, Glumac S, Pavlović S, Borković-Mitić S, Grigorov I, Stanković S, Pejić S, Todorović A, Drakulić D, Jasnić N, Đorđević J, Todorović Z. Efekti pretretmana meldonijumom na tokove različitih modela sepsi kod pacova. in Knjiga sažetaka: Treći Kongres biologa Srbije: Osnovna i primenjena istraživanja: Metodika nastave; 2022 Sep 21-25; Zlatibor, Serbia. 2022;:340.
https://hdl.handle.net/21.15107/rcub_ibiss_5933 .
Lakić, Iva, Đurašević, Siniša, Ružičić, Aleksandra, Tosti, Tomislav, Đurović, Saša, Glumac, Sofija, Pavlović, Slađan, Borković-Mitić, Slavica, Grigorov, Ilijana, Stanković, Sanja, Pejić, Snežana, Todorović, Ana, Drakulić, Dunja, Jasnić, Nebojša, Đorđević, Jelena, Todorović, Zoran, "Efekti pretretmana meldonijumom na tokove različitih modela sepsi kod pacova" in Knjiga sažetaka: Treći Kongres biologa Srbije: Osnovna i primenjena istraživanja: Metodika nastave; 2022 Sep 21-25; Zlatibor, Serbia (2022):340,
https://hdl.handle.net/21.15107/rcub_ibiss_5933 .

Progesterone exerts protective effects in rat permanent bilateral common carotid artery occlusion model

Guševac Stojanović, Ivana; Tatalović, Nikola; Veljković, Filip; Martinović, Jelena; Zarić Kontić, Marina; Blagojević, Duško; Stojanović, Zoran; Drakulić, Dunja

(European College of Neuropsychopharmacology (ECNP), 2022)

TY  - CONF
AU  - Guševac Stojanović, Ivana
AU  - Tatalović, Nikola
AU  - Veljković, Filip
AU  - Martinović, Jelena
AU  - Zarić Kontić, Marina
AU  - Blagojević, Duško
AU  - Stojanović, Zoran
AU  - Drakulić, Dunja
PY  - 2022
UR  - https://www.ecnp.eu/congress2022/ECNPcongress/programme/programme#!abstractdetails/0000506150
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/5315
AB  - Introduction: Cerebral hypoperfusion (CH), a reduced cerebral blood flow, characteristic for aging and neurodegenerative disorders, might be associated with a pro-oxidative state in the brain due to the generation of reactive oxygen species (ROS) that cause neuronal damage. These overgenerated pro-oxidants might be reduced, disabled and neutralized by the endogenous antioxidant enzymes, including superoxide dismutase (SOD) and catalase (CAT). A sex steroid hormone, progesterone, in several experimental models of neuronal injury exerts anti-oxidative properties upregulating anti-oxidative molecules and thus promoting neuroprotection. However, its efficacy in the state of CH is still unknown and it is necessary to better understand the mechanism underlying this hormone’s neuroprotective effects.
Aim: We investigated whether progesterone is able to modulate CH-induced pro-oxidative/anti-oxidative imbalance, as well as SOD and CAT activities, in the prefrontal cortex of three-month-old male Wistar rats subjected to permanent bilateral common carotid artery occlusion (2VO).
Methods: The appropriate actions were undertaken to reduce the distress of the animals in agreement with the European Community Council Directive of 86/609/EEC and 010/63/EU for animal experiments. All experimental procedures were allowed by the Ethical Committee for the Use of Laboratory Animals of VINČA Institute of Nuclear Sciences - National Institute of thе Republic of Serbia, University of Belgrade, Belgrade, Republic of Serbia (protocol authorization numbers 02/11 and 323-07-04253/2016-05). Following chloral hydrate anaesthesia, 8 rats randomly assigned in 2VO groups were double occluded with 5–0 silk suture, while 4 animals from sham operated group were subjected to the same surgical procedure but without actual ligation of carotid arteries. Four hours following the surgical procedure animals from sham operated group, used as controls, were subcutaneously treated with vehicle (commercial flax oil, 1 mg/kg/day, S + V), while animals in 2VO groups were subjected to either progesterone (1.7 mg/kg/day, 2VO + P) or vehicle (commercial flax oil, 1 mg/kg/day, 2VO + V). Following 7 days lasting treatments, pro-oxidative/anti-oxidative balance was assessed according to the method of Alamdari et al. [1]; while activities of anti-oxidative enzymes were determined as described in the study by Tatalović et al. [2]. One-way analysis of variance (ANOVA) test followed by Tukey’s post hoc test was employed to analyse data. The values of p < 0.05 or less were considered statistically significant.
Results: Obtained results demonstrate that compared to controls, 2VO and vehicle treatment induced a significant increase of pro-oxidants levels (p < 0.01) as well as the activities of both investigated anti-oxidative enzymes, although only the CAT activity was significantly increased (p < 0.05). Following progesterone treatment, pro-oxidants levels were lowered to the control level which caused the difference between the 2VO groups (p < 0.05). In parallel, no statistically significant change in SOD activity was observed, while CAT was upregulated (p < 0.05).
Conclusion: Presented results suggest that in the prefrontal cortex in the state of CH, progesterone, by modulating the CAT activity, downregulates overgenerated reactive species, reduces CH-induced oxidative stress and exerts anti-oxidative outcomes.
The Ministry of Education, Science and Technological Development


Disclosure statement: Financially supported by The Ministry of Education, Science and Technological Development, grants No 451-03-1/2022-14/13 and 451-03-68/2022-14/ 200007 and 13451-03-68/2022-14/ 200175




 
[1] Alamdari, D.H., Ghayour-Mobarhan, M., Tavallaie, S., Parizadeh, M.R., Moohebati, M., Ghafoori, F., et al., 2008. Prooxidant–antioxidant balance as a new risk factor in patients with angiographically defined coronary artery disease. Clinical Biochemistry 41(6),375–380. 
[2] Tatalović, N., Vidonja Uzelac, T., Oreščanin Dušić, Z., Nikolić-Kokić, A., Bresjanac, M., Blagojević, D., 2021. Ibogaine-Mediated ROS/Antioxidant Elevation in Isolated Rat Uterus Is β-Adrenergic Receptors and KATP Channels Mediated. Antioxidants 10(11),1792.
PB  - European College of Neuropsychopharmacology (ECNP)
C3  - The 35th ECNP Congress; 2023 Oct 7-10; Barcelona, Spain
T1  - Progesterone exerts protective effects in rat permanent bilateral common carotid artery occlusion model
IS  - P.0477
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_5315
ER  - 
@conference{
author = "Guševac Stojanović, Ivana and Tatalović, Nikola and Veljković, Filip and Martinović, Jelena and Zarić Kontić, Marina and Blagojević, Duško and Stojanović, Zoran and Drakulić, Dunja",
year = "2022",
abstract = "Introduction: Cerebral hypoperfusion (CH), a reduced cerebral blood flow, characteristic for aging and neurodegenerative disorders, might be associated with a pro-oxidative state in the brain due to the generation of reactive oxygen species (ROS) that cause neuronal damage. These overgenerated pro-oxidants might be reduced, disabled and neutralized by the endogenous antioxidant enzymes, including superoxide dismutase (SOD) and catalase (CAT). A sex steroid hormone, progesterone, in several experimental models of neuronal injury exerts anti-oxidative properties upregulating anti-oxidative molecules and thus promoting neuroprotection. However, its efficacy in the state of CH is still unknown and it is necessary to better understand the mechanism underlying this hormone’s neuroprotective effects.
Aim: We investigated whether progesterone is able to modulate CH-induced pro-oxidative/anti-oxidative imbalance, as well as SOD and CAT activities, in the prefrontal cortex of three-month-old male Wistar rats subjected to permanent bilateral common carotid artery occlusion (2VO).
Methods: The appropriate actions were undertaken to reduce the distress of the animals in agreement with the European Community Council Directive of 86/609/EEC and 010/63/EU for animal experiments. All experimental procedures were allowed by the Ethical Committee for the Use of Laboratory Animals of VINČA Institute of Nuclear Sciences - National Institute of thе Republic of Serbia, University of Belgrade, Belgrade, Republic of Serbia (protocol authorization numbers 02/11 and 323-07-04253/2016-05). Following chloral hydrate anaesthesia, 8 rats randomly assigned in 2VO groups were double occluded with 5–0 silk suture, while 4 animals from sham operated group were subjected to the same surgical procedure but without actual ligation of carotid arteries. Four hours following the surgical procedure animals from sham operated group, used as controls, were subcutaneously treated with vehicle (commercial flax oil, 1 mg/kg/day, S + V), while animals in 2VO groups were subjected to either progesterone (1.7 mg/kg/day, 2VO + P) or vehicle (commercial flax oil, 1 mg/kg/day, 2VO + V). Following 7 days lasting treatments, pro-oxidative/anti-oxidative balance was assessed according to the method of Alamdari et al. [1]; while activities of anti-oxidative enzymes were determined as described in the study by Tatalović et al. [2]. One-way analysis of variance (ANOVA) test followed by Tukey’s post hoc test was employed to analyse data. The values of p < 0.05 or less were considered statistically significant.
Results: Obtained results demonstrate that compared to controls, 2VO and vehicle treatment induced a significant increase of pro-oxidants levels (p < 0.01) as well as the activities of both investigated anti-oxidative enzymes, although only the CAT activity was significantly increased (p < 0.05). Following progesterone treatment, pro-oxidants levels were lowered to the control level which caused the difference between the 2VO groups (p < 0.05). In parallel, no statistically significant change in SOD activity was observed, while CAT was upregulated (p < 0.05).
Conclusion: Presented results suggest that in the prefrontal cortex in the state of CH, progesterone, by modulating the CAT activity, downregulates overgenerated reactive species, reduces CH-induced oxidative stress and exerts anti-oxidative outcomes.
The Ministry of Education, Science and Technological Development


Disclosure statement: Financially supported by The Ministry of Education, Science and Technological Development, grants No 451-03-1/2022-14/13 and 451-03-68/2022-14/ 200007 and 13451-03-68/2022-14/ 200175




 
[1] Alamdari, D.H., Ghayour-Mobarhan, M., Tavallaie, S., Parizadeh, M.R., Moohebati, M., Ghafoori, F., et al., 2008. Prooxidant–antioxidant balance as a new risk factor in patients with angiographically defined coronary artery disease. Clinical Biochemistry 41(6),375–380. 
[2] Tatalović, N., Vidonja Uzelac, T., Oreščanin Dušić, Z., Nikolić-Kokić, A., Bresjanac, M., Blagojević, D., 2021. Ibogaine-Mediated ROS/Antioxidant Elevation in Isolated Rat Uterus Is β-Adrenergic Receptors and KATP Channels Mediated. Antioxidants 10(11),1792.",
publisher = "European College of Neuropsychopharmacology (ECNP)",
journal = "The 35th ECNP Congress; 2023 Oct 7-10; Barcelona, Spain",
title = "Progesterone exerts protective effects in rat permanent bilateral common carotid artery occlusion model",
number = "P.0477",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_5315"
}
Guševac Stojanović, I., Tatalović, N., Veljković, F., Martinović, J., Zarić Kontić, M., Blagojević, D., Stojanović, Z.,& Drakulić, D.. (2022). Progesterone exerts protective effects in rat permanent bilateral common carotid artery occlusion model. in The 35th ECNP Congress; 2023 Oct 7-10; Barcelona, Spain
European College of Neuropsychopharmacology (ECNP).(P.0477).
https://hdl.handle.net/21.15107/rcub_ibiss_5315
Guševac Stojanović I, Tatalović N, Veljković F, Martinović J, Zarić Kontić M, Blagojević D, Stojanović Z, Drakulić D. Progesterone exerts protective effects in rat permanent bilateral common carotid artery occlusion model. in The 35th ECNP Congress; 2023 Oct 7-10; Barcelona, Spain. 2022;(P.0477).
https://hdl.handle.net/21.15107/rcub_ibiss_5315 .
Guševac Stojanović, Ivana, Tatalović, Nikola, Veljković, Filip, Martinović, Jelena, Zarić Kontić, Marina, Blagojević, Duško, Stojanović, Zoran, Drakulić, Dunja, "Progesterone exerts protective effects in rat permanent bilateral common carotid artery occlusion model" in The 35th ECNP Congress; 2023 Oct 7-10; Barcelona, Spain, no. P.0477 (2022),
https://hdl.handle.net/21.15107/rcub_ibiss_5315 .

Cerebral hypoperfusion and progesterone treatment alter parameters of oxidative stress and antioxidant defence in male rats

Guševac Stojanović, Ivana; Todorović, Ana; Pejić, Snežana; Tatalović, Nikola; Blagojević, Duško; Martinović, Jelena; Grković, Ivana; Mitrović, Nataša; Zarić, Marina; Drakulić, Dunja

(Belgrade: Society of Physical Chemists of Serbia, 2021)

TY  - CONF
AU  - Guševac Stojanović, Ivana
AU  - Todorović, Ana
AU  - Pejić, Snežana
AU  - Tatalović, Nikola
AU  - Blagojević, Duško
AU  - Martinović, Jelena
AU  - Grković, Ivana
AU  - Mitrović, Nataša
AU  - Zarić, Marina
AU  - Drakulić, Dunja
PY  - 2021
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/5247
AB  - Numerous natural compounds, like progesterone (P4), a sex steroid hormone, are highlighted as promising agents for treatment of different disorders including prolonged disturbance of blood flow. However, its action on several oxidative stress markers (pro/antioxidant balance, products of lipid peroxidation and phosphatidylcholine to lysophosphatidylcholine intensity ratio) and one of the major components of antioxidant system, superoxide dismutase in rat prefrontal cortex (PFC) following permanent bilateral occlusion of common carotid arteries (2VO) is not completely investigated. According to the obtained results, levels of investigated oxidative stress markers and SOD activity were altered in 2VO animals treated with vehicle, while P4 treatment returned them to control values. Overall, presented data indicate that P4 might manifest antioxidative features in PFC of 2VO rats.
PB  - Belgrade: Society of Physical Chemists of Serbia
C3  - Proceeding: 15th International Conference on Fundamental and Applied Aspects of Physical Chemistry: Physical Chemistry 2021: the Conference is dedicated to the 30th Anniversary of the founding of the Society of Physical Chemists of Serbia and 100th Anniversary of Bray-Liebhafsky reaction. Vol. 1; 2021 Sep 20-24; Belgrade, Serbia
T1  - Cerebral hypoperfusion and progesterone treatment alter parameters of oxidative stress and antioxidant defence in male rats
VL  - 1
SP  - 25
EP  - 32
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_5247
ER  - 
@conference{
author = "Guševac Stojanović, Ivana and Todorović, Ana and Pejić, Snežana and Tatalović, Nikola and Blagojević, Duško and Martinović, Jelena and Grković, Ivana and Mitrović, Nataša and Zarić, Marina and Drakulić, Dunja",
year = "2021",
abstract = "Numerous natural compounds, like progesterone (P4), a sex steroid hormone, are highlighted as promising agents for treatment of different disorders including prolonged disturbance of blood flow. However, its action on several oxidative stress markers (pro/antioxidant balance, products of lipid peroxidation and phosphatidylcholine to lysophosphatidylcholine intensity ratio) and one of the major components of antioxidant system, superoxide dismutase in rat prefrontal cortex (PFC) following permanent bilateral occlusion of common carotid arteries (2VO) is not completely investigated. According to the obtained results, levels of investigated oxidative stress markers and SOD activity were altered in 2VO animals treated with vehicle, while P4 treatment returned them to control values. Overall, presented data indicate that P4 might manifest antioxidative features in PFC of 2VO rats.",
publisher = "Belgrade: Society of Physical Chemists of Serbia",
journal = "Proceeding: 15th International Conference on Fundamental and Applied Aspects of Physical Chemistry: Physical Chemistry 2021: the Conference is dedicated to the 30th Anniversary of the founding of the Society of Physical Chemists of Serbia and 100th Anniversary of Bray-Liebhafsky reaction. Vol. 1; 2021 Sep 20-24; Belgrade, Serbia",
title = "Cerebral hypoperfusion and progesterone treatment alter parameters of oxidative stress and antioxidant defence in male rats",
volume = "1",
pages = "25-32",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_5247"
}
Guševac Stojanović, I., Todorović, A., Pejić, S., Tatalović, N., Blagojević, D., Martinović, J., Grković, I., Mitrović, N., Zarić, M.,& Drakulić, D.. (2021). Cerebral hypoperfusion and progesterone treatment alter parameters of oxidative stress and antioxidant defence in male rats. in Proceeding: 15th International Conference on Fundamental and Applied Aspects of Physical Chemistry: Physical Chemistry 2021: the Conference is dedicated to the 30th Anniversary of the founding of the Society of Physical Chemists of Serbia and 100th Anniversary of Bray-Liebhafsky reaction. Vol. 1; 2021 Sep 20-24; Belgrade, Serbia
Belgrade: Society of Physical Chemists of Serbia., 1, 25-32.
https://hdl.handle.net/21.15107/rcub_ibiss_5247
Guševac Stojanović I, Todorović A, Pejić S, Tatalović N, Blagojević D, Martinović J, Grković I, Mitrović N, Zarić M, Drakulić D. Cerebral hypoperfusion and progesterone treatment alter parameters of oxidative stress and antioxidant defence in male rats. in Proceeding: 15th International Conference on Fundamental and Applied Aspects of Physical Chemistry: Physical Chemistry 2021: the Conference is dedicated to the 30th Anniversary of the founding of the Society of Physical Chemists of Serbia and 100th Anniversary of Bray-Liebhafsky reaction. Vol. 1; 2021 Sep 20-24; Belgrade, Serbia. 2021;1:25-32.
https://hdl.handle.net/21.15107/rcub_ibiss_5247 .
Guševac Stojanović, Ivana, Todorović, Ana, Pejić, Snežana, Tatalović, Nikola, Blagojević, Duško, Martinović, Jelena, Grković, Ivana, Mitrović, Nataša, Zarić, Marina, Drakulić, Dunja, "Cerebral hypoperfusion and progesterone treatment alter parameters of oxidative stress and antioxidant defence in male rats" in Proceeding: 15th International Conference on Fundamental and Applied Aspects of Physical Chemistry: Physical Chemistry 2021: the Conference is dedicated to the 30th Anniversary of the founding of the Society of Physical Chemists of Serbia and 100th Anniversary of Bray-Liebhafsky reaction. Vol. 1; 2021 Sep 20-24; Belgrade, Serbia, 1 (2021):25-32,
https://hdl.handle.net/21.15107/rcub_ibiss_5247 .

Effects of fullerene C60 supplementation on gut microbiota and glucose and lipid homeostasis in rats

Đurašević, Siniša; Nikolić, Gorana; Todorović, Ana; Drakulić, Dunja; Pejić, Snežana; Martinović, Vesna; Mitić-Ćulafić, Dragana; Milić, Dragana; Kop, Tatjana J.; Jasnić, Nebojša; Đorđević, Jelena; Todorović, Zoran

(2020)

TY  - JOUR
AU  - Đurašević, Siniša
AU  - Nikolić, Gorana
AU  - Todorović, Ana
AU  - Drakulić, Dunja
AU  - Pejić, Snežana
AU  - Martinović, Vesna
AU  - Mitić-Ćulafić, Dragana
AU  - Milić, Dragana
AU  - Kop, Tatjana J.
AU  - Jasnić, Nebojša
AU  - Đorđević, Jelena
AU  - Todorović, Zoran
PY  - 2020
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3645
AB  - The effects of twelve weeks of supplementation with fullerene C60 olive/coconut oil solution on a broad spectrum of parameters in rats were examined. The tissue bioaccumulation of C60 was shown to be tissue-specific, with the liver, heart, and adrenal glands being the organs of the greatest, and the kidney, brain, and spleen being the organs of the smallest accumulation. C60 did not change aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase serum activities level, nor the damage of liver cells DNA. There were no effects of fullerene on prooxidant-antioxidant balance in the liver, kidney, spleen, heart, and brain, nor any visible harmful effects on the liver, heart, aorta, spleen, kidney, and small intestine histology. Fullerene changed the gut microbiota structure towards the bacteria that ameliorate lipid homeostasis, causing a serum triglycerides concentration decrease. However, C60 significantly increased the insulin resistance, serum ascorbate oxidation, and brain malondialdehyde and advanced oxidation protein products level. The deteriorative effects of C60 on the brain and serum could be attributed to the specific physicochemical composition of these tissues, potentiating the C60 aggregation or biotransformation as the key element of its pro-oxidative action.
T2  - Food and Chemical Toxicology
T1  - Effects of fullerene C60 supplementation on gut microbiota and glucose and lipid homeostasis in rats
VL  - 140
DO  - 10.1016/j.fct.2020.111302
SP  - 111302
ER  - 
@article{
author = "Đurašević, Siniša and Nikolić, Gorana and Todorović, Ana and Drakulić, Dunja and Pejić, Snežana and Martinović, Vesna and Mitić-Ćulafić, Dragana and Milić, Dragana and Kop, Tatjana J. and Jasnić, Nebojša and Đorđević, Jelena and Todorović, Zoran",
year = "2020",
abstract = "The effects of twelve weeks of supplementation with fullerene C60 olive/coconut oil solution on a broad spectrum of parameters in rats were examined. The tissue bioaccumulation of C60 was shown to be tissue-specific, with the liver, heart, and adrenal glands being the organs of the greatest, and the kidney, brain, and spleen being the organs of the smallest accumulation. C60 did not change aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase serum activities level, nor the damage of liver cells DNA. There were no effects of fullerene on prooxidant-antioxidant balance in the liver, kidney, spleen, heart, and brain, nor any visible harmful effects on the liver, heart, aorta, spleen, kidney, and small intestine histology. Fullerene changed the gut microbiota structure towards the bacteria that ameliorate lipid homeostasis, causing a serum triglycerides concentration decrease. However, C60 significantly increased the insulin resistance, serum ascorbate oxidation, and brain malondialdehyde and advanced oxidation protein products level. The deteriorative effects of C60 on the brain and serum could be attributed to the specific physicochemical composition of these tissues, potentiating the C60 aggregation or biotransformation as the key element of its pro-oxidative action.",
journal = "Food and Chemical Toxicology",
title = "Effects of fullerene C60 supplementation on gut microbiota and glucose and lipid homeostasis in rats",
volume = "140",
doi = "10.1016/j.fct.2020.111302",
pages = "111302"
}
Đurašević, S., Nikolić, G., Todorović, A., Drakulić, D., Pejić, S., Martinović, V., Mitić-Ćulafić, D., Milić, D., Kop, T. J., Jasnić, N., Đorđević, J.,& Todorović, Z.. (2020). Effects of fullerene C60 supplementation on gut microbiota and glucose and lipid homeostasis in rats. in Food and Chemical Toxicology, 140, 111302.
https://doi.org/10.1016/j.fct.2020.111302
Đurašević S, Nikolić G, Todorović A, Drakulić D, Pejić S, Martinović V, Mitić-Ćulafić D, Milić D, Kop TJ, Jasnić N, Đorđević J, Todorović Z. Effects of fullerene C60 supplementation on gut microbiota and glucose and lipid homeostasis in rats. in Food and Chemical Toxicology. 2020;140:111302.
doi:10.1016/j.fct.2020.111302 .
Đurašević, Siniša, Nikolić, Gorana, Todorović, Ana, Drakulić, Dunja, Pejić, Snežana, Martinović, Vesna, Mitić-Ćulafić, Dragana, Milić, Dragana, Kop, Tatjana J., Jasnić, Nebojša, Đorđević, Jelena, Todorović, Zoran, "Effects of fullerene C60 supplementation on gut microbiota and glucose and lipid homeostasis in rats" in Food and Chemical Toxicology, 140 (2020):111302,
https://doi.org/10.1016/j.fct.2020.111302 . .
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Progesterone downscales oxidative stress and boosts antioxidant defense capacity in rat model of permanent common carotid artery occlusion

Guševac, Ivana; Tatalović, Nikola; Zarić, Marina; Martinović, Jelena; Mitrović, Nataša; Blagojević, Duško; Grković, Ivana; Drakulić, Dunja

(Brussels, Belgium : Federation of European Neurocience Societies, 2018)

TY  - CONF
AU  - Guševac, Ivana
AU  - Tatalović, Nikola
AU  - Zarić, Marina
AU  - Martinović, Jelena
AU  - Mitrović, Nataša
AU  - Blagojević, Duško
AU  - Grković, Ivana
AU  - Drakulić, Dunja
PY  - 2018
UR  - https://forum2018.fens.org/
UR  - https://radar.ibiss.bg.ac.rs/123456789/3897
AB  - Potent neurosteroid progesterone (P4) strongly influences functional recovery in
various models of neurological diseases. However, its protective antioxidative
potential is not well established in stance of chronic cerebral hypoperfusion (CCH)
that induces ischemic milieu in the brain. CCH results in a cascade of events
leading to uncontrolled generation of 4-hydroxynonenal (HNE), a hallmark of
oxidative stress that can be abolished by mitochondrial antioxidant enzyme
manganese superoxide dismutase (MnSOD). Post-ischemic brain regeneration
requires preservation of cerebral blood flow that could be achieved by production of
vasodilatator nitric oxide (NO), synthesized by endothelial NO synthase (eNOS)
whose actions are regulated by phosphorylation at various sites. Decreased
phosphorylation of eNOS at Thr495 during antioxidative response, promotes its
activity and NO production, contributing to neuroprotection. Given the scarcity of
data about P4 antioxidative actions in prefrontal cortex during CCH, current study
assessed the level of HNE and NO, as well as MnSOD activity and the extent of
eNOS phosphorylation at Thr495 in rats subjected to sham operation and injected
with vehicle (commercial flax oil) or animals with permanent occlusion of common
carotid arteries and treated either with vehicle or P4 (1.7 mg/kg/day) for 7 days.
Results indicate that P4 decreases CCH-induced HNE generation and MnSOD
activity, diminishes inactivation of eNOS and increases production of protective NO.
In conclusion, P4 might downscale oxidative stress and boost antioxidant defense
capacity in CCH model, pointing investigated parameters as potential targets of P4
neuroprotective actions. Financially supported by MNTPR RS, grants 173044 and
41014.
PB  - Brussels, Belgium : Federation of European Neurocience Societies
C3  - 11th FENS Forum of Neuroscience
T1  - Progesterone downscales oxidative stress and boosts antioxidant defense capacity in rat model of permanent common carotid artery occlusion
SP  - 1971
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_3897
ER  - 
@conference{
author = "Guševac, Ivana and Tatalović, Nikola and Zarić, Marina and Martinović, Jelena and Mitrović, Nataša and Blagojević, Duško and Grković, Ivana and Drakulić, Dunja",
year = "2018",
abstract = "Potent neurosteroid progesterone (P4) strongly influences functional recovery in
various models of neurological diseases. However, its protective antioxidative
potential is not well established in stance of chronic cerebral hypoperfusion (CCH)
that induces ischemic milieu in the brain. CCH results in a cascade of events
leading to uncontrolled generation of 4-hydroxynonenal (HNE), a hallmark of
oxidative stress that can be abolished by mitochondrial antioxidant enzyme
manganese superoxide dismutase (MnSOD). Post-ischemic brain regeneration
requires preservation of cerebral blood flow that could be achieved by production of
vasodilatator nitric oxide (NO), synthesized by endothelial NO synthase (eNOS)
whose actions are regulated by phosphorylation at various sites. Decreased
phosphorylation of eNOS at Thr495 during antioxidative response, promotes its
activity and NO production, contributing to neuroprotection. Given the scarcity of
data about P4 antioxidative actions in prefrontal cortex during CCH, current study
assessed the level of HNE and NO, as well as MnSOD activity and the extent of
eNOS phosphorylation at Thr495 in rats subjected to sham operation and injected
with vehicle (commercial flax oil) or animals with permanent occlusion of common
carotid arteries and treated either with vehicle or P4 (1.7 mg/kg/day) for 7 days.
Results indicate that P4 decreases CCH-induced HNE generation and MnSOD
activity, diminishes inactivation of eNOS and increases production of protective NO.
In conclusion, P4 might downscale oxidative stress and boost antioxidant defense
capacity in CCH model, pointing investigated parameters as potential targets of P4
neuroprotective actions. Financially supported by MNTPR RS, grants 173044 and
41014.",
publisher = "Brussels, Belgium : Federation of European Neurocience Societies",
journal = "11th FENS Forum of Neuroscience",
title = "Progesterone downscales oxidative stress and boosts antioxidant defense capacity in rat model of permanent common carotid artery occlusion",
pages = "1971",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_3897"
}
Guševac, I., Tatalović, N., Zarić, M., Martinović, J., Mitrović, N., Blagojević, D., Grković, I.,& Drakulić, D.. (2018). Progesterone downscales oxidative stress and boosts antioxidant defense capacity in rat model of permanent common carotid artery occlusion. in 11th FENS Forum of Neuroscience
Brussels, Belgium : Federation of European Neurocience Societies., 1971.
https://hdl.handle.net/21.15107/rcub_ibiss_3897
Guševac I, Tatalović N, Zarić M, Martinović J, Mitrović N, Blagojević D, Grković I, Drakulić D. Progesterone downscales oxidative stress and boosts antioxidant defense capacity in rat model of permanent common carotid artery occlusion. in 11th FENS Forum of Neuroscience. 2018;:1971.
https://hdl.handle.net/21.15107/rcub_ibiss_3897 .
Guševac, Ivana, Tatalović, Nikola, Zarić, Marina, Martinović, Jelena, Mitrović, Nataša, Blagojević, Duško, Grković, Ivana, Drakulić, Dunja, "Progesterone downscales oxidative stress and boosts antioxidant defense capacity in rat model of permanent common carotid artery occlusion" in 11th FENS Forum of Neuroscience (2018):1971,
https://hdl.handle.net/21.15107/rcub_ibiss_3897 .

Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development

Grković, Ivana; Bjelobaba, Ivana; Mitrović, Nataša; Lavrnja, Irena; Drakulić, Dunja; Martinović, Jelena; Stanojlović, Miloš; Horvat, Anica; Nedeljković, Nadežda

(Amsterdam: Elsevier Science Publisher, 2016)

TY  - JOUR
AU  - Grković, Ivana
AU  - Bjelobaba, Ivana
AU  - Mitrović, Nataša
AU  - Lavrnja, Irena
AU  - Drakulić, Dunja
AU  - Martinović, Jelena
AU  - Stanojlović, Miloš
AU  - Horvat, Anica
AU  - Nedeljković, Nadežda
PY  - 2016
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/5977
AB  - Nucleoside triphosphate diphosphohydrolase3 (NTPDase3) is membrane-bound ectoenzyme which hydrolyzes extracellular ATP, thus modulating the function of purinergicreceptors and the pattern of purinergic signaling. Here we analyzed the developmentalexpression of NTPDase3 in female hypothalamus, cerebral cortex and hippocampal formationat different postnatal ages (PD7–PD90) by qRT-PCR and immunohistochemistry. Inhypothalamus and hippocampus, a similar developmental profile was seen: NTPDase3 geneexpression was stable during postnatal development and increased in adults. In the cortex,upregulation of NTPDase3 mRNA expression was seen at PD15 and further increase wasevidenced in adults. Immunohistochemical analysis at PD7 revealed faint neuronal NTPDase3localization, in dorsal hypothalamus. The immunoreactivity (ir) gradually increased in PD15and PD20, in clusters of cells in the lateral, ventral and dorsomedial hypothalamus.Furthermore, in PD20 animals, NTPDase3-ir was detected on short fibers in the posteriorhypothalamic area, while in PD30 the fibers appeared progressively longer and markedlyvaricose. In adults, the strongest NTPDase3-ir was observed in collections of cells indorsomedial hypothalamic nucleus, dorsal and lateral hypothalamus and in several thalamicareas, whereas the varicose fibers traversed entire diencephalon, particularly paraventricularthalamic nucleus, ventromedial and dorsomedial hypothalamic nuclei, the arcuate nucleus andthe prefornical part of the lateral hypothalamus. The presumably ascending NTPDase3-irfibers were first observed in PD20; their density and the varicose appearance increased untilthe adulthood. Prominent enhancement of NTPDase3-ir in the hypothalamus coincides withage when animals acquire diurnal rhythms of sleeping and feeding, supporting the hypothesisthat this enzyme may be involved in regulation of homeostatic functions.
PB  - Amsterdam: Elsevier Science Publisher
T2  - Journal of chemical neuroanatomy
T1  - Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development
VL  - 77
DO  - 10.1016/j.jchemneu.2016.04.001
SP  - 10
EP  - 18
ER  - 
@article{
author = "Grković, Ivana and Bjelobaba, Ivana and Mitrović, Nataša and Lavrnja, Irena and Drakulić, Dunja and Martinović, Jelena and Stanojlović, Miloš and Horvat, Anica and Nedeljković, Nadežda",
year = "2016",
abstract = "Nucleoside triphosphate diphosphohydrolase3 (NTPDase3) is membrane-bound ectoenzyme which hydrolyzes extracellular ATP, thus modulating the function of purinergicreceptors and the pattern of purinergic signaling. Here we analyzed the developmentalexpression of NTPDase3 in female hypothalamus, cerebral cortex and hippocampal formationat different postnatal ages (PD7–PD90) by qRT-PCR and immunohistochemistry. Inhypothalamus and hippocampus, a similar developmental profile was seen: NTPDase3 geneexpression was stable during postnatal development and increased in adults. In the cortex,upregulation of NTPDase3 mRNA expression was seen at PD15 and further increase wasevidenced in adults. Immunohistochemical analysis at PD7 revealed faint neuronal NTPDase3localization, in dorsal hypothalamus. The immunoreactivity (ir) gradually increased in PD15and PD20, in clusters of cells in the lateral, ventral and dorsomedial hypothalamus.Furthermore, in PD20 animals, NTPDase3-ir was detected on short fibers in the posteriorhypothalamic area, while in PD30 the fibers appeared progressively longer and markedlyvaricose. In adults, the strongest NTPDase3-ir was observed in collections of cells indorsomedial hypothalamic nucleus, dorsal and lateral hypothalamus and in several thalamicareas, whereas the varicose fibers traversed entire diencephalon, particularly paraventricularthalamic nucleus, ventromedial and dorsomedial hypothalamic nuclei, the arcuate nucleus andthe prefornical part of the lateral hypothalamus. The presumably ascending NTPDase3-irfibers were first observed in PD20; their density and the varicose appearance increased untilthe adulthood. Prominent enhancement of NTPDase3-ir in the hypothalamus coincides withage when animals acquire diurnal rhythms of sleeping and feeding, supporting the hypothesisthat this enzyme may be involved in regulation of homeostatic functions.",
publisher = "Amsterdam: Elsevier Science Publisher",
journal = "Journal of chemical neuroanatomy",
title = "Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development",
volume = "77",
doi = "10.1016/j.jchemneu.2016.04.001",
pages = "10-18"
}
Grković, I., Bjelobaba, I., Mitrović, N., Lavrnja, I., Drakulić, D., Martinović, J., Stanojlović, M., Horvat, A.,& Nedeljković, N.. (2016). Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development. in Journal of chemical neuroanatomy
Amsterdam: Elsevier Science Publisher., 77, 10-18.
https://doi.org/10.1016/j.jchemneu.2016.04.001
Grković I, Bjelobaba I, Mitrović N, Lavrnja I, Drakulić D, Martinović J, Stanojlović M, Horvat A, Nedeljković N. Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development. in Journal of chemical neuroanatomy. 2016;77:10-18.
doi:10.1016/j.jchemneu.2016.04.001 .
Grković, Ivana, Bjelobaba, Ivana, Mitrović, Nataša, Lavrnja, Irena, Drakulić, Dunja, Martinović, Jelena, Stanojlović, Miloš, Horvat, Anica, Nedeljković, Nadežda, "Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development" in Journal of chemical neuroanatomy, 77 (2016):10-18,
https://doi.org/10.1016/j.jchemneu.2016.04.001 . .
1
8
5
8

Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development

Grković, Ivana; Bjelobaba, Ivana; Mitrović, Nataša; Lavrnja, Irena; Drakulić, Dunja; Martinović, Jelena; Stanojlović, Miloš; Horvat, Anica; Nedeljković, Nadežda

(Amsterdam: Elsevier Science Publisher, 2016)

TY  - JOUR
AU  - Grković, Ivana
AU  - Bjelobaba, Ivana
AU  - Mitrović, Nataša
AU  - Lavrnja, Irena
AU  - Drakulić, Dunja
AU  - Martinović, Jelena
AU  - Stanojlović, Miloš
AU  - Horvat, Anica
AU  - Nedeljković, Nadežda
PY  - 2016
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/5976
AB  - Nucleoside triphosphate diphosphohydrolase3 (NTPDase3) is membrane-bound ectoenzyme which hydrolyzes extracellular ATP, thus modulating the function of purinergic
receptors and the pattern of purinergic signaling. Here we analyzed the developmental
expression of NTPDase3 in female hypothalamus, cerebral cortex and hippocampal formation
at different postnatal ages (PD7–PD90) by qRT-PCR and immunohistochemistry. In
hypothalamus and hippocampus, a similar developmental profile was seen: NTPDase3 gene
expression was stable during postnatal development and increased in adults. In the cortex,
upregulation of NTPDase3 mRNA expression was seen at PD15 and further increase was
evidenced in adults. Immunohistochemical analysis at PD7 revealed faint neuronal NTPDase3
localization, in dorsal hypothalamus. The immunoreactivity (ir) gradually increased in PD15
and PD20, in clusters of cells in the lateral, ventral and dorsomedial hypothalamus.
Furthermore, in PD20 animals, NTPDase3-ir was detected on short fibers in the posterior
hypothalamic area, while in PD30 the fibers appeared progressively longer and markedly
varicose. In adults, the strongest NTPDase3-ir was observed in collections of cells in
dorsomedial hypothalamic nucleus, dorsal and lateral hypothalamus and in several thalamic
areas, whereas the varicose fibers traversed entire diencephalon, particularly paraventricular
thalamic nucleus, ventromedial and dorsomedial hypothalamic nuclei, the arcuate nucleus and
the prefornical part of the lateral hypothalamus. The presumably ascending NTPDase3-ir
fibers were first observed in PD20; their density and the varicose appearance increased until
the adulthood. Prominent enhancement of NTPDase3-ir in the hypothalamus coincides with
age when animals acquire diurnal rhythms of sleeping and feeding, supporting the hypothesis
that this enzyme may be involved in regulation of homeostatic functions.
PB  - Amsterdam: Elsevier Science Publisher
T2  - Journal of chemical neuroanatomy
T1  - Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development
VL  - 77
DO  - 10.1016/j.jchemneu.2016.04.001
SP  - 10
EP  - 18
ER  - 
@article{
author = "Grković, Ivana and Bjelobaba, Ivana and Mitrović, Nataša and Lavrnja, Irena and Drakulić, Dunja and Martinović, Jelena and Stanojlović, Miloš and Horvat, Anica and Nedeljković, Nadežda",
year = "2016",
abstract = "Nucleoside triphosphate diphosphohydrolase3 (NTPDase3) is membrane-bound ectoenzyme which hydrolyzes extracellular ATP, thus modulating the function of purinergic
receptors and the pattern of purinergic signaling. Here we analyzed the developmental
expression of NTPDase3 in female hypothalamus, cerebral cortex and hippocampal formation
at different postnatal ages (PD7–PD90) by qRT-PCR and immunohistochemistry. In
hypothalamus and hippocampus, a similar developmental profile was seen: NTPDase3 gene
expression was stable during postnatal development and increased in adults. In the cortex,
upregulation of NTPDase3 mRNA expression was seen at PD15 and further increase was
evidenced in adults. Immunohistochemical analysis at PD7 revealed faint neuronal NTPDase3
localization, in dorsal hypothalamus. The immunoreactivity (ir) gradually increased in PD15
and PD20, in clusters of cells in the lateral, ventral and dorsomedial hypothalamus.
Furthermore, in PD20 animals, NTPDase3-ir was detected on short fibers in the posterior
hypothalamic area, while in PD30 the fibers appeared progressively longer and markedly
varicose. In adults, the strongest NTPDase3-ir was observed in collections of cells in
dorsomedial hypothalamic nucleus, dorsal and lateral hypothalamus and in several thalamic
areas, whereas the varicose fibers traversed entire diencephalon, particularly paraventricular
thalamic nucleus, ventromedial and dorsomedial hypothalamic nuclei, the arcuate nucleus and
the prefornical part of the lateral hypothalamus. The presumably ascending NTPDase3-ir
fibers were first observed in PD20; their density and the varicose appearance increased until
the adulthood. Prominent enhancement of NTPDase3-ir in the hypothalamus coincides with
age when animals acquire diurnal rhythms of sleeping and feeding, supporting the hypothesis
that this enzyme may be involved in regulation of homeostatic functions.",
publisher = "Amsterdam: Elsevier Science Publisher",
journal = "Journal of chemical neuroanatomy",
title = "Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development",
volume = "77",
doi = "10.1016/j.jchemneu.2016.04.001",
pages = "10-18"
}
Grković, I., Bjelobaba, I., Mitrović, N., Lavrnja, I., Drakulić, D., Martinović, J., Stanojlović, M., Horvat, A.,& Nedeljković, N.. (2016). Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development. in Journal of chemical neuroanatomy
Amsterdam: Elsevier Science Publisher., 77, 10-18.
https://doi.org/10.1016/j.jchemneu.2016.04.001
Grković I, Bjelobaba I, Mitrović N, Lavrnja I, Drakulić D, Martinović J, Stanojlović M, Horvat A, Nedeljković N. Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development. in Journal of chemical neuroanatomy. 2016;77:10-18.
doi:10.1016/j.jchemneu.2016.04.001 .
Grković, Ivana, Bjelobaba, Ivana, Mitrović, Nataša, Lavrnja, Irena, Drakulić, Dunja, Martinović, Jelena, Stanojlović, Miloš, Horvat, Anica, Nedeljković, Nadežda, "Expression of ecto-nucleoside triphosphate diphosphohydrolase3 (NTPDase3) in the female rat brain during postnatal development" in Journal of chemical neuroanatomy, 77 (2016):10-18,
https://doi.org/10.1016/j.jchemneu.2016.04.001 . .
1
8
5
8

Low-Dose Dexamethasone Treatment Promotes the Pro-Survival Signalling Pathway in the Adult Rat Prefrontal Cortex

Drakulić, Dunja R; Veličković, Nataša; Stanojlović, Milos R; Grković, Ivana S; Mitrović, N; Lavrnja, Irena; Horvat, Anica I

(2013)

TY  - JOUR
AU  - Drakulić, Dunja R
AU  - Veličković, Nataša
AU  - Stanojlović, Milos  R
AU  - Grković, Ivana S
AU  - Mitrović, N
AU  - Lavrnja, Irena
AU  - Horvat, Anica I
PY  - 2013
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/994
AB  - Synthetic glucocorticoid dexamethasone (DEX), a highly potent anti-inflammatory and immunosuppressive agent, is widely used in the treatment of brain cancer, as well as for inflammatory and autoimmune diseases. The present study aimed to determine whether low-dose subchronic DEX treatment (100g/kg for eight consecutive days) exerts long-term effects on apoptosis in the adult rat prefrontal cortex (PFC) by examining the expression of cell death-promoting molecules [poly(ADP-ribose) polymerase (PARP), p53, procaspase 3, cleaved caspase 3, Bax] and cell-survival molecules (AKT, Bcl-2). The results obtained revealed that body, thymus and adrenal gland weights, as well corticosterone levels, in the serum and PFC were reduced 1day after the last DEX injection. In the PFC, DEX caused activation of AKT, augmentation of pro-survival Bcl-2 protein and an enhanced Bcl-2/Bax protein ratio, as well Bcl-2 translocation to the mitochondria. An unaltered profile with respect to the protein expression of apoptotic molecules PARP, procaspase 3 and Bax was detected, whereas p53 protein was decreased. Reverse transcriptase -polymerase chain reaction analysis showed a decrease of p53 mRNA levels and no significant difference in Bcl-2 and Bax mRNA expression in DEX-treated rats. Finally, a DNA fragmentation assay and Fluoro-Jade staining demonstrated no considerable changes in apoptosis in the rat PFC. Our findings support the concept that low-dose DEX creates a hypocorticoid state in the brain and also indicate that subchronic DEX treatment activates the pro-survival signalling pathway but does not change apoptotic markers in the rat PFC. This mechanism might be relevant for the DEX-induced apoptosis resistance observed during and after chemotherapy of patients with brain tumours.
T2  - Journal of Neuroendocrinology
T1  - Low-Dose Dexamethasone Treatment Promotes the Pro-Survival Signalling Pathway in the Adult Rat Prefrontal Cortex
IS  - 7
VL  - 25
SP  - 125
EP  - 616
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_994
ER  - 
@article{
author = "Drakulić, Dunja R and Veličković, Nataša and Stanojlović, Milos  R and Grković, Ivana S and Mitrović, N and Lavrnja, Irena and Horvat, Anica I",
year = "2013",
abstract = "Synthetic glucocorticoid dexamethasone (DEX), a highly potent anti-inflammatory and immunosuppressive agent, is widely used in the treatment of brain cancer, as well as for inflammatory and autoimmune diseases. The present study aimed to determine whether low-dose subchronic DEX treatment (100g/kg for eight consecutive days) exerts long-term effects on apoptosis in the adult rat prefrontal cortex (PFC) by examining the expression of cell death-promoting molecules [poly(ADP-ribose) polymerase (PARP), p53, procaspase 3, cleaved caspase 3, Bax] and cell-survival molecules (AKT, Bcl-2). The results obtained revealed that body, thymus and adrenal gland weights, as well corticosterone levels, in the serum and PFC were reduced 1day after the last DEX injection. In the PFC, DEX caused activation of AKT, augmentation of pro-survival Bcl-2 protein and an enhanced Bcl-2/Bax protein ratio, as well Bcl-2 translocation to the mitochondria. An unaltered profile with respect to the protein expression of apoptotic molecules PARP, procaspase 3 and Bax was detected, whereas p53 protein was decreased. Reverse transcriptase -polymerase chain reaction analysis showed a decrease of p53 mRNA levels and no significant difference in Bcl-2 and Bax mRNA expression in DEX-treated rats. Finally, a DNA fragmentation assay and Fluoro-Jade staining demonstrated no considerable changes in apoptosis in the rat PFC. Our findings support the concept that low-dose DEX creates a hypocorticoid state in the brain and also indicate that subchronic DEX treatment activates the pro-survival signalling pathway but does not change apoptotic markers in the rat PFC. This mechanism might be relevant for the DEX-induced apoptosis resistance observed during and after chemotherapy of patients with brain tumours.",
journal = "Journal of Neuroendocrinology",
title = "Low-Dose Dexamethasone Treatment Promotes the Pro-Survival Signalling Pathway in the Adult Rat Prefrontal Cortex",
number = "7",
volume = "25",
pages = "125-616",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_994"
}
Drakulić, D. R., Veličković, N., Stanojlović, Milos  R, Grković, I. S., Mitrović, N., Lavrnja, I.,& Horvat, A. I.. (2013). Low-Dose Dexamethasone Treatment Promotes the Pro-Survival Signalling Pathway in the Adult Rat Prefrontal Cortex. in Journal of Neuroendocrinology, 25(7), 125-616.
https://hdl.handle.net/21.15107/rcub_ibiss_994
Drakulić DR, Veličković N, Stanojlović, Milos  R, Grković IS, Mitrović N, Lavrnja I, Horvat AI. Low-Dose Dexamethasone Treatment Promotes the Pro-Survival Signalling Pathway in the Adult Rat Prefrontal Cortex. in Journal of Neuroendocrinology. 2013;25(7):125-616.
https://hdl.handle.net/21.15107/rcub_ibiss_994 .
Drakulić, Dunja R, Veličković, Nataša, Stanojlović, Milos  R, Grković, Ivana S, Mitrović, N, Lavrnja, Irena, Horvat, Anica I, "Low-Dose Dexamethasone Treatment Promotes the Pro-Survival Signalling Pathway in the Adult Rat Prefrontal Cortex" in Journal of Neuroendocrinology, 25, no. 7 (2013):125-616,
https://hdl.handle.net/21.15107/rcub_ibiss_994 .

Time-Course of Hypothalamic-Pituitary-Adrenal Axis Activity and Inflammation in Juvenile Rat Brain After Cranial Irradiation

Veličković, Nataša; Drakulić, Dunja R; Petrović, Snjezana B; Grković, Ivana S; Milosević, Maja S; Stanojlović, Milos R; Horvat, Anica I

(2012)

TY  - JOUR
AU  - Veličković, Nataša
AU  - Drakulić, Dunja R
AU  - Petrović, Snjezana B
AU  - Grković, Ivana S
AU  - Milosević, Maja S
AU  - Stanojlović, Milos  R
AU  - Horvat, Anica I
PY  - 2012
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/1104
AB  - Recent studies reported that exposure of juvenile rats to cranial irradiation affects hypothalamic-pituitary-adrenal (HPA) axis stability, leading to its activation along with radiation-induced inflammation. In the present study, we hypothesized whether inflammatory reaction in the CNS could be a mediator of HPA axis response to cranial irradiation (CI). Therefore, we analyzed time-course changes of serum corticosterone level, as well IL-1 beta and TNF-alpha level in the serum and hypothalamus of juvenile rats after CI. Protein and gene expression of the glucocorticoid receptor (GR) and nuclear factor kappaB (NF kappa B) were examined in the hippocampus within 24 h postirradiation interval. Cranial irradiation led to rapid induction of both GR and NF kappa B mRNA and protein in the hippocampus at 1 h. The increment in NF kappa B protein persisted for 2 h, therefore NF kappa B/GR protein ratio was turned in favor of NF kappa B. Central inflammation was characterized by increased IL-1 beta in the hypothalamus, with maximum levels at 2 and 4 h after irradiation, while both IL-1 beta and TNF-alpha were undetectable in the serum. Enhanced hypothalamic IL-1 beta probably induced the relocation of hippocampal NF kappa B to the nucleus and decreased NF kappa B mRNA at 6 h, indicating promotion of inflammation in the key tissue for HPA axis regulation. Concomitant increase of corticosterone level and enhanced GR nuclear translocation in the hippocampus at 6 h might represent a compensatory mechanism for observed inflammation. Our results indicate that acute radiation response is characterized by increased central inflammation and concomitant HPA axis activation, most likely having a role in protection of the organism from overwhelming inflammatory reaction.
T2  - Cellular and Molecular Neurobiology
T1  - Time-Course of Hypothalamic-Pituitary-Adrenal Axis Activity and Inflammation in Juvenile Rat Brain After Cranial Irradiation
IS  - 7
VL  - 32
SP  - 129
EP  - 1185
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_1104
ER  - 
@article{
author = "Veličković, Nataša and Drakulić, Dunja R and Petrović, Snjezana B and Grković, Ivana S and Milosević, Maja S and Stanojlović, Milos  R and Horvat, Anica I",
year = "2012",
abstract = "Recent studies reported that exposure of juvenile rats to cranial irradiation affects hypothalamic-pituitary-adrenal (HPA) axis stability, leading to its activation along with radiation-induced inflammation. In the present study, we hypothesized whether inflammatory reaction in the CNS could be a mediator of HPA axis response to cranial irradiation (CI). Therefore, we analyzed time-course changes of serum corticosterone level, as well IL-1 beta and TNF-alpha level in the serum and hypothalamus of juvenile rats after CI. Protein and gene expression of the glucocorticoid receptor (GR) and nuclear factor kappaB (NF kappa B) were examined in the hippocampus within 24 h postirradiation interval. Cranial irradiation led to rapid induction of both GR and NF kappa B mRNA and protein in the hippocampus at 1 h. The increment in NF kappa B protein persisted for 2 h, therefore NF kappa B/GR protein ratio was turned in favor of NF kappa B. Central inflammation was characterized by increased IL-1 beta in the hypothalamus, with maximum levels at 2 and 4 h after irradiation, while both IL-1 beta and TNF-alpha were undetectable in the serum. Enhanced hypothalamic IL-1 beta probably induced the relocation of hippocampal NF kappa B to the nucleus and decreased NF kappa B mRNA at 6 h, indicating promotion of inflammation in the key tissue for HPA axis regulation. Concomitant increase of corticosterone level and enhanced GR nuclear translocation in the hippocampus at 6 h might represent a compensatory mechanism for observed inflammation. Our results indicate that acute radiation response is characterized by increased central inflammation and concomitant HPA axis activation, most likely having a role in protection of the organism from overwhelming inflammatory reaction.",
journal = "Cellular and Molecular Neurobiology",
title = "Time-Course of Hypothalamic-Pituitary-Adrenal Axis Activity and Inflammation in Juvenile Rat Brain After Cranial Irradiation",
number = "7",
volume = "32",
pages = "129-1185",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_1104"
}
Veličković, N., Drakulić, D. R., Petrović, S. B., Grković, I. S., Milosević, M. S., Stanojlović, Milos  R,& Horvat, A. I.. (2012). Time-Course of Hypothalamic-Pituitary-Adrenal Axis Activity and Inflammation in Juvenile Rat Brain After Cranial Irradiation. in Cellular and Molecular Neurobiology, 32(7), 129-1185.
https://hdl.handle.net/21.15107/rcub_ibiss_1104
Veličković N, Drakulić DR, Petrović SB, Grković IS, Milosević MS, Stanojlović, Milos  R, Horvat AI. Time-Course of Hypothalamic-Pituitary-Adrenal Axis Activity and Inflammation in Juvenile Rat Brain After Cranial Irradiation. in Cellular and Molecular Neurobiology. 2012;32(7):129-1185.
https://hdl.handle.net/21.15107/rcub_ibiss_1104 .
Veličković, Nataša, Drakulić, Dunja R, Petrović, Snjezana B, Grković, Ivana S, Milosević, Maja S, Stanojlović, Milos  R, Horvat, Anica I, "Time-Course of Hypothalamic-Pituitary-Adrenal Axis Activity and Inflammation in Juvenile Rat Brain After Cranial Irradiation" in Cellular and Molecular Neurobiology, 32, no. 7 (2012):129-1185,
https://hdl.handle.net/21.15107/rcub_ibiss_1104 .

Ontogenetic profile of ecto-5 '-nucleotidase in rat brain synaptic plasma membranes

Stanojević, Ivana; Bjelobaba, Ivana; Nedeljković, Nadežda N.; Drakulić, Dunja R.; Petrović, Snježana B.; Stojiljković, Mirjana B.; Horvat, Anica I.

(John Wiley and Sons, 2011)

TY  - JOUR
AU  - Stanojević, Ivana
AU  - Bjelobaba, Ivana
AU  - Nedeljković, Nadežda N.
AU  - Drakulić, Dunja R.
AU  - Petrović, Snježana B.
AU  - Stojiljković, Mirjana B.
AU  - Horvat, Anica I.
PY  - 2011
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/1286
AB  - Ecto-5'-nucleotidase (CD73; EC 3.1.3.5, e-5NT) is regarded as the key enzyme in the extracellular formation of adenosine, which acts as a neuromodulator and important trophic and homeostatic factor in the brain. In the present study, we have investigated e-5NT activity, kinetic properties concerning AMP hydrolysis and the enzyme protein abundance in the purified synaptic plasma membrane (SPM) preparations isolated from whole female rat brain at different ages. We observed pronounced increase in AMP hydrolyzing activity in SPM during maturation, with greatest increment between juvenile (15-day-old) and pre-pubertal (30-day-old) rats. Immunodetection of e-5NT protein in the SPM displayed the reverse pattern of expression, with the maximum relative abundance at juvenile and minimum relative abundance in the adult stage. Negative correlation between the enzyme activity and the enzyme protein abundance in the SPM indicates that e-5NT has additional roles in the synaptic compartment during postnatal brain development, other than those related to AMP hydrolysis. Determination of kinetic parameters, K(m) and V(max), suggested that the increase in the enzyme activity with maturation was entirely due to the increase in the enzyme catalytic efficiency (V(max)/K(m)). Finally, double immunofluorescence staining against e-5NT and presynaptic membrane marker syntaxin provided first direct evidence for the existence of this ecto-enzyme in the presynaptic compartment. The results of the study suggest that e-5NT may be a part of general scheme of brain development and synapse maturation and provide rationale for the previously reported inconsistencies between enzyme immunohistochemical and biochemical studies concerning localization of e-5NT in the brain. (C) 2011 ISDN. Published by Elsevier Ltd. All rights reserved.
PB  - John Wiley and Sons
T2  - International Journal of Developmental Neuroscience
T1  - Ontogenetic profile of ecto-5 '-nucleotidase in rat brain synaptic plasma membranes
IS  - 4
VL  - 29
DO  - 10.1016/j.ijdevneu.2011.03.003
SP  - 397
EP  - 403
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_1286
ER  - 
@article{
author = "Stanojević, Ivana and Bjelobaba, Ivana and Nedeljković, Nadežda N. and Drakulić, Dunja R. and Petrović, Snježana B. and Stojiljković, Mirjana B. and Horvat, Anica I.",
year = "2011",
abstract = "Ecto-5'-nucleotidase (CD73; EC 3.1.3.5, e-5NT) is regarded as the key enzyme in the extracellular formation of adenosine, which acts as a neuromodulator and important trophic and homeostatic factor in the brain. In the present study, we have investigated e-5NT activity, kinetic properties concerning AMP hydrolysis and the enzyme protein abundance in the purified synaptic plasma membrane (SPM) preparations isolated from whole female rat brain at different ages. We observed pronounced increase in AMP hydrolyzing activity in SPM during maturation, with greatest increment between juvenile (15-day-old) and pre-pubertal (30-day-old) rats. Immunodetection of e-5NT protein in the SPM displayed the reverse pattern of expression, with the maximum relative abundance at juvenile and minimum relative abundance in the adult stage. Negative correlation between the enzyme activity and the enzyme protein abundance in the SPM indicates that e-5NT has additional roles in the synaptic compartment during postnatal brain development, other than those related to AMP hydrolysis. Determination of kinetic parameters, K(m) and V(max), suggested that the increase in the enzyme activity with maturation was entirely due to the increase in the enzyme catalytic efficiency (V(max)/K(m)). Finally, double immunofluorescence staining against e-5NT and presynaptic membrane marker syntaxin provided first direct evidence for the existence of this ecto-enzyme in the presynaptic compartment. The results of the study suggest that e-5NT may be a part of general scheme of brain development and synapse maturation and provide rationale for the previously reported inconsistencies between enzyme immunohistochemical and biochemical studies concerning localization of e-5NT in the brain. (C) 2011 ISDN. Published by Elsevier Ltd. All rights reserved.",
publisher = "John Wiley and Sons",
journal = "International Journal of Developmental Neuroscience",
title = "Ontogenetic profile of ecto-5 '-nucleotidase in rat brain synaptic plasma membranes",
number = "4",
volume = "29",
doi = "10.1016/j.ijdevneu.2011.03.003",
pages = "397-403",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_1286"
}
Stanojević, I., Bjelobaba, I., Nedeljković, N. N., Drakulić, D. R., Petrović, S. B., Stojiljković, M. B.,& Horvat, A. I.. (2011). Ontogenetic profile of ecto-5 '-nucleotidase in rat brain synaptic plasma membranes. in International Journal of Developmental Neuroscience
John Wiley and Sons., 29(4), 397-403.
https://doi.org/10.1016/j.ijdevneu.2011.03.003
https://hdl.handle.net/21.15107/rcub_ibiss_1286
Stanojević I, Bjelobaba I, Nedeljković NN, Drakulić DR, Petrović SB, Stojiljković MB, Horvat AI. Ontogenetic profile of ecto-5 '-nucleotidase in rat brain synaptic plasma membranes. in International Journal of Developmental Neuroscience. 2011;29(4):397-403.
doi:10.1016/j.ijdevneu.2011.03.003
https://hdl.handle.net/21.15107/rcub_ibiss_1286 .
Stanojević, Ivana, Bjelobaba, Ivana, Nedeljković, Nadežda N., Drakulić, Dunja R., Petrović, Snježana B., Stojiljković, Mirjana B., Horvat, Anica I., "Ontogenetic profile of ecto-5 '-nucleotidase in rat brain synaptic plasma membranes" in International Journal of Developmental Neuroscience, 29, no. 4 (2011):397-403,
https://doi.org/10.1016/j.ijdevneu.2011.03.003 .,
https://hdl.handle.net/21.15107/rcub_ibiss_1286 .
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Inhibition of Mitochondrial Na+-Dependent Ca2+ Efflux By 17 Beta-Estradiol in the Rat Hippocampus

Petrović, Snjezana B; Veličković, Nataša; Stanojević, Ivana; Milosević, Maja S; Drakulić, Dunja R; Stanojlović, Milos R; Horvat, Anica I

(2011)

TY  - JOUR
AU  - Petrović, Snjezana B
AU  - Veličković, Nataša
AU  - Stanojević, Ivana
AU  - Milosević, Maja S
AU  - Drakulić, Dunja R
AU  - Stanojlović, Milos  R
AU  - Horvat, Anica I
PY  - 2011
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/1265
AB  - Our results, as well as those of others, have indicated that 17 beta-estradiol (E2) exerts its nongenomic effects in neuronal cells by affecting plasma membrane Ca2+ flux. In neuronal cells mitochondria possess Ca2+ buffering properties as they both sequester and release Ca2+. The goal of this study was to examine the rapid non-genomic effect of E2 on mitochondria! Ca2+ transport in hippocampal synaptosomes from ovariectomised rats. In addition, we aimed to determine if, and to what extent, E2 receptors participated in mitochondria! Ca2+ transport modulation by E2 in vitro. E2-specific binding and Ca2+ transport was monitored. At physiological E2 concentrations (0.1-1.5 nmol/L), specific E2 binding to mitochondria isolated from hippocampal synaptosomes was detected with a B-max and K-m of 37.6 +/- 2.6 fmol/mg protein and 0.69 +/- 0.14 nmol/L of free E2, respectively. The main mitochondrial Ca2+ influx mechanism is the Ruthenium Red-sensitive uniporter driven by mitochondrial membrane potential. Despite no effect of E2 on Ca2+ influx, a physiological E2 concentration (0.5 nmol/L) protected mitochondrial membrane potential and consequently Ca2+ influx from the uncoupling agent carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (1 mu mol/L). In neuronal cells the predominant mitochondria! Ca2+ efflux mechanism is the Na+/Ca2+ exchanger. E2 caused Ca2+ efflux inhibition (by 46%) coupled with increased affinity of the Na+/Ca2+ exchanger for Na+. Using E2 receptor (ER alpha and ER beta) antagonists and agonists, we confirmed ER beta's involvement in E2-induced mitochondrial membrane potential protection as well as Ca2+ efflux inhibition. In summary, our results indicate that the nongenomic neuromodulatory role of E2 in rat hippocampus is achieved by affecting mitochondria! Ca2+ transport via, in part, mitochondrial ER beta. (C) 2011 IBRO. Published by Elsevier Ltd. All rights reserved.
T2  - Neuroscience
T1  - Inhibition of Mitochondrial Na+-Dependent Ca2+ Efflux By 17 Beta-Estradiol in the Rat Hippocampus
IS  - null
VL  - 192
EP  - 204
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_1265
ER  - 
@article{
author = "Petrović, Snjezana B and Veličković, Nataša and Stanojević, Ivana and Milosević, Maja S and Drakulić, Dunja R and Stanojlović, Milos  R and Horvat, Anica I",
year = "2011",
abstract = "Our results, as well as those of others, have indicated that 17 beta-estradiol (E2) exerts its nongenomic effects in neuronal cells by affecting plasma membrane Ca2+ flux. In neuronal cells mitochondria possess Ca2+ buffering properties as they both sequester and release Ca2+. The goal of this study was to examine the rapid non-genomic effect of E2 on mitochondria! Ca2+ transport in hippocampal synaptosomes from ovariectomised rats. In addition, we aimed to determine if, and to what extent, E2 receptors participated in mitochondria! Ca2+ transport modulation by E2 in vitro. E2-specific binding and Ca2+ transport was monitored. At physiological E2 concentrations (0.1-1.5 nmol/L), specific E2 binding to mitochondria isolated from hippocampal synaptosomes was detected with a B-max and K-m of 37.6 +/- 2.6 fmol/mg protein and 0.69 +/- 0.14 nmol/L of free E2, respectively. The main mitochondrial Ca2+ influx mechanism is the Ruthenium Red-sensitive uniporter driven by mitochondrial membrane potential. Despite no effect of E2 on Ca2+ influx, a physiological E2 concentration (0.5 nmol/L) protected mitochondrial membrane potential and consequently Ca2+ influx from the uncoupling agent carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (1 mu mol/L). In neuronal cells the predominant mitochondria! Ca2+ efflux mechanism is the Na+/Ca2+ exchanger. E2 caused Ca2+ efflux inhibition (by 46%) coupled with increased affinity of the Na+/Ca2+ exchanger for Na+. Using E2 receptor (ER alpha and ER beta) antagonists and agonists, we confirmed ER beta's involvement in E2-induced mitochondrial membrane potential protection as well as Ca2+ efflux inhibition. In summary, our results indicate that the nongenomic neuromodulatory role of E2 in rat hippocampus is achieved by affecting mitochondria! Ca2+ transport via, in part, mitochondrial ER beta. (C) 2011 IBRO. Published by Elsevier Ltd. All rights reserved.",
journal = "Neuroscience",
title = "Inhibition of Mitochondrial Na+-Dependent Ca2+ Efflux By 17 Beta-Estradiol in the Rat Hippocampus",
number = "null",
volume = "192",
pages = "204",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_1265"
}
Petrović, S. B., Veličković, N., Stanojević, I., Milosević, M. S., Drakulić, D. R., Stanojlović, Milos  R,& Horvat, A. I.. (2011). Inhibition of Mitochondrial Na+-Dependent Ca2+ Efflux By 17 Beta-Estradiol in the Rat Hippocampus. in Neuroscience, 192(null).
https://hdl.handle.net/21.15107/rcub_ibiss_1265
Petrović SB, Veličković N, Stanojević I, Milosević MS, Drakulić DR, Stanojlović, Milos  R, Horvat AI. Inhibition of Mitochondrial Na+-Dependent Ca2+ Efflux By 17 Beta-Estradiol in the Rat Hippocampus. in Neuroscience. 2011;192(null):null-204.
https://hdl.handle.net/21.15107/rcub_ibiss_1265 .
Petrović, Snjezana B, Veličković, Nataša, Stanojević, Ivana, Milosević, Maja S, Drakulić, Dunja R, Stanojlović, Milos  R, Horvat, Anica I, "Inhibition of Mitochondrial Na+-Dependent Ca2+ Efflux By 17 Beta-Estradiol in the Rat Hippocampus" in Neuroscience, 192, no. null (2011),
https://hdl.handle.net/21.15107/rcub_ibiss_1265 .