Jelenković, Ankica

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  • Jelenković, Ankica (8)
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Author's Bibliography

Effects of Vitamin D3 on the NADPH Oxidase and Matrix Metalloproteinase 9 in an Animal Model of Global Cerebral Ischemia.

Velimirović, Milica; Jevtić Dožudić, Gordana; Selaković, Vesna; Stojković, Tihomir; Puškaš, Nela; Zaletel, Ivan; Živković, Milica; Dragutinović, Vesna; Nikolić, Tatjana; Jelenković, Ankica; Đorović, Đorđe; Mirčić, Aleksandar; Petronijević, Nataša D.

(2018)

TY  - JOUR
AU  - Velimirović, Milica
AU  - Jevtić Dožudić, Gordana
AU  - Selaković, Vesna
AU  - Stojković, Tihomir
AU  - Puškaš, Nela
AU  - Zaletel, Ivan
AU  - Živković, Milica
AU  - Dragutinović, Vesna
AU  - Nikolić, Tatjana
AU  - Jelenković, Ankica
AU  - Đorović, Đorđe
AU  - Mirčić, Aleksandar
AU  - Petronijević, Nataša D.
PY  - 2018
UR  - https://www.hindawi.com/journals/omcl/2018/3273654/
UR  - http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC5932460
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3167
AB  - Decreased blood flow in the brain leads to a rapid increase in reactive oxygen species (ROS). NADPH oxidase (NOX) is an enzyme family that has the physiological function to produce ROS. NOX2 and NOX4 overexpression is associated with aggravated ischemic injury, while NOX2/4-deficient mice had reduced stroke size. Dysregulation of matrix metalloproteinases (MMPs) contributes to tissue damage. The active form of vitamin D3 expresses neuroprotective, immunomodulatory, and anti-inflammatory effects in the CNS. The present study examines the effects of the vitamin D3 pretreatment on the oxidative stress parameters and the expression of NOX subunits, MMP9, microglial marker Iba1, and vitamin D receptor (VDR), in the cortex and hippocampus of Mongolian gerbils subjected to ten minutes of global cerebral ischemia, followed by 24 hours of reperfusion. The ischemia/reperfusion procedure has induced oxidative stress, changes in the expression of NOX2 subunits and MMP9 in the brain, and increased MMP9 activity in the serum of experimental animals. Pretreatment with vitamin D3 was especially effective on NOX2 subunits, MMP9, and the level of malondialdehyde and superoxide anion. These results outline the significance of the NOX and MMP9 investigation in brain ischemia and the importance of adequate vitamin D supplementation in ameliorating the injury caused by I/R.
T2  - Oxidative medicine and cellular longevity
T1  - Effects of Vitamin D3 on the NADPH Oxidase and Matrix Metalloproteinase 9 in an Animal Model of Global Cerebral Ischemia.
VL  - 2018
DO  - 10.1155/2018/3273654
SP  - 3273654
ER  - 
@article{
author = "Velimirović, Milica and Jevtić Dožudić, Gordana and Selaković, Vesna and Stojković, Tihomir and Puškaš, Nela and Zaletel, Ivan and Živković, Milica and Dragutinović, Vesna and Nikolić, Tatjana and Jelenković, Ankica and Đorović, Đorđe and Mirčić, Aleksandar and Petronijević, Nataša D.",
year = "2018",
abstract = "Decreased blood flow in the brain leads to a rapid increase in reactive oxygen species (ROS). NADPH oxidase (NOX) is an enzyme family that has the physiological function to produce ROS. NOX2 and NOX4 overexpression is associated with aggravated ischemic injury, while NOX2/4-deficient mice had reduced stroke size. Dysregulation of matrix metalloproteinases (MMPs) contributes to tissue damage. The active form of vitamin D3 expresses neuroprotective, immunomodulatory, and anti-inflammatory effects in the CNS. The present study examines the effects of the vitamin D3 pretreatment on the oxidative stress parameters and the expression of NOX subunits, MMP9, microglial marker Iba1, and vitamin D receptor (VDR), in the cortex and hippocampus of Mongolian gerbils subjected to ten minutes of global cerebral ischemia, followed by 24 hours of reperfusion. The ischemia/reperfusion procedure has induced oxidative stress, changes in the expression of NOX2 subunits and MMP9 in the brain, and increased MMP9 activity in the serum of experimental animals. Pretreatment with vitamin D3 was especially effective on NOX2 subunits, MMP9, and the level of malondialdehyde and superoxide anion. These results outline the significance of the NOX and MMP9 investigation in brain ischemia and the importance of adequate vitamin D supplementation in ameliorating the injury caused by I/R.",
journal = "Oxidative medicine and cellular longevity",
title = "Effects of Vitamin D3 on the NADPH Oxidase and Matrix Metalloproteinase 9 in an Animal Model of Global Cerebral Ischemia.",
volume = "2018",
doi = "10.1155/2018/3273654",
pages = "3273654"
}
Velimirović, M., Jevtić Dožudić, G., Selaković, V., Stojković, T., Puškaš, N., Zaletel, I., Živković, M., Dragutinović, V., Nikolić, T., Jelenković, A., Đorović, Đ., Mirčić, A.,& Petronijević, N. D.. (2018). Effects of Vitamin D3 on the NADPH Oxidase and Matrix Metalloproteinase 9 in an Animal Model of Global Cerebral Ischemia.. in Oxidative medicine and cellular longevity, 2018, 3273654.
https://doi.org/10.1155/2018/3273654
Velimirović M, Jevtić Dožudić G, Selaković V, Stojković T, Puškaš N, Zaletel I, Živković M, Dragutinović V, Nikolić T, Jelenković A, Đorović Đ, Mirčić A, Petronijević ND. Effects of Vitamin D3 on the NADPH Oxidase and Matrix Metalloproteinase 9 in an Animal Model of Global Cerebral Ischemia.. in Oxidative medicine and cellular longevity. 2018;2018:3273654.
doi:10.1155/2018/3273654 .
Velimirović, Milica, Jevtić Dožudić, Gordana, Selaković, Vesna, Stojković, Tihomir, Puškaš, Nela, Zaletel, Ivan, Živković, Milica, Dragutinović, Vesna, Nikolić, Tatjana, Jelenković, Ankica, Đorović, Đorđe, Mirčić, Aleksandar, Petronijević, Nataša D., "Effects of Vitamin D3 on the NADPH Oxidase and Matrix Metalloproteinase 9 in an Animal Model of Global Cerebral Ischemia." in Oxidative medicine and cellular longevity, 2018 (2018):3273654,
https://doi.org/10.1155/2018/3273654 . .
36
17
33

Aluminum neurotoxicity: From subtle molecular lesions to neurological diseases

Jelenković, Ankica

(Nova Science Publishers, Inc., New York, 2016)

TY  - BOOK
PY  - 2016
UR  - https://www.novapublishers.com/catalog/product_info.php?products_id=57596&osCsid=57a0e63e53cf827e95b97b9bdbd404f6
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/2774
AB  - Aluminum is the third most abundant element in the Earth’s crust. In many of the previous experimental, epidemiological, pathohistological, biochemical and other research studies, aluminum, accumulated from the environment has been recognized as a very harmful substance to the human body. Aluminum intake usually happens unintentionally due to the fact that people know little about its prevalence in water, factory-processed foods, medicines, cosmetics, etc. When accumulated in human organs, it can cause severe damage, and even lead to chronic neurodegenerative diseases. Both oxidative and nitrosative stress can be the leading cause or contribute to its toxic effects in humans and animals. All of this is supported by the fact that mitochondrial dysfunction is the earliest stage of aluminum neurotoxicity. When oxidative damage occurs under the effects of free radicals, together with the decreased antioxidant protection - due to the decreased production of the chemical energy molecule (adenosine triphosphate) as well as reducing equivalents (both in and out of mitochondria) - then the conditions for the occurrence of a vicious circle in aluminum neurotoxicity are created. Aluminum also significantly interferes with the main steps of the synaptic neurotransmission, which may lead to the progression of neuropathies. The glutamate-glutamine pathway and numerous neurotransmitter transporters are affected as well. Oxidative stress and the disruption of neurotransmission do not only exist when adult individuals are exposed to this neurotoxin, but also in individuals prenatally exposed to it as well, and these are expressed after birth. Numerous research studies, both in animals and humans, ex vivo and in vitro, quite clearly showed that aluminum can be associated with chronic neurodegenerative diseases. Additionally, there is a positive correlation between the exposure to aluminum and the pathophysiology of Alzheimer’s, Parkinson’s, Huntington’s disease, amyotrophic lateral sclerosis, and so on. One of the possible mechanisms for the generation/development of these diseases could be the disturbed homeostasis of essential metals and the appearance of unfolded or misfolded proteins that are mostly specific for a particular disease. In those research studies, the influence of aluminum on the generation of beta-amyloid, alpha synuclein, etc. was satisfactorily examined. It is very difficult, however, to suppress aluminum neurotoxicity, as well as development and progression of the diseases caused by or associated with aluminum. This is the result of some complex mechanisms through which aluminum causes its deleterious effects, and which are also responsible for the existence of multiple targets for aluminum. It is, therefore, necessary to know how these mechanisms induce the damage, in order to be able to prevent or treat the damage once it occurs. A large number of substances, including active components in traditional medicine, medical drugs and substances which are used only experimentally, have been examined so far. The results of studies conducted so far are inconclusive and they require further research. According to all the aforementioned findings, it may be concluded that well-planned, prospective and randomized clinical trials are necessary in order to use any of these substances in humans.
PB  - Nova Science Publishers, Inc., New York
T2  - Aluminum Neurotoxicity: From Subtle Molecular Lesions to Neurological Diseases
T1  - Aluminum neurotoxicity: From subtle molecular lesions to neurological diseases
SP  - 1
EP  - 168
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_2774
ER  - 
@book{
editor = "Jelenković, Ankica",
year = "2016",
abstract = "Aluminum is the third most abundant element in the Earth’s crust. In many of the previous experimental, epidemiological, pathohistological, biochemical and other research studies, aluminum, accumulated from the environment has been recognized as a very harmful substance to the human body. Aluminum intake usually happens unintentionally due to the fact that people know little about its prevalence in water, factory-processed foods, medicines, cosmetics, etc. When accumulated in human organs, it can cause severe damage, and even lead to chronic neurodegenerative diseases. Both oxidative and nitrosative stress can be the leading cause or contribute to its toxic effects in humans and animals. All of this is supported by the fact that mitochondrial dysfunction is the earliest stage of aluminum neurotoxicity. When oxidative damage occurs under the effects of free radicals, together with the decreased antioxidant protection - due to the decreased production of the chemical energy molecule (adenosine triphosphate) as well as reducing equivalents (both in and out of mitochondria) - then the conditions for the occurrence of a vicious circle in aluminum neurotoxicity are created. Aluminum also significantly interferes with the main steps of the synaptic neurotransmission, which may lead to the progression of neuropathies. The glutamate-glutamine pathway and numerous neurotransmitter transporters are affected as well. Oxidative stress and the disruption of neurotransmission do not only exist when adult individuals are exposed to this neurotoxin, but also in individuals prenatally exposed to it as well, and these are expressed after birth. Numerous research studies, both in animals and humans, ex vivo and in vitro, quite clearly showed that aluminum can be associated with chronic neurodegenerative diseases. Additionally, there is a positive correlation between the exposure to aluminum and the pathophysiology of Alzheimer’s, Parkinson’s, Huntington’s disease, amyotrophic lateral sclerosis, and so on. One of the possible mechanisms for the generation/development of these diseases could be the disturbed homeostasis of essential metals and the appearance of unfolded or misfolded proteins that are mostly specific for a particular disease. In those research studies, the influence of aluminum on the generation of beta-amyloid, alpha synuclein, etc. was satisfactorily examined. It is very difficult, however, to suppress aluminum neurotoxicity, as well as development and progression of the diseases caused by or associated with aluminum. This is the result of some complex mechanisms through which aluminum causes its deleterious effects, and which are also responsible for the existence of multiple targets for aluminum. It is, therefore, necessary to know how these mechanisms induce the damage, in order to be able to prevent or treat the damage once it occurs. A large number of substances, including active components in traditional medicine, medical drugs and substances which are used only experimentally, have been examined so far. The results of studies conducted so far are inconclusive and they require further research. According to all the aforementioned findings, it may be concluded that well-planned, prospective and randomized clinical trials are necessary in order to use any of these substances in humans.",
publisher = "Nova Science Publishers, Inc., New York",
journal = "Aluminum Neurotoxicity: From Subtle Molecular Lesions to Neurological Diseases",
title = "Aluminum neurotoxicity: From subtle molecular lesions to neurological diseases",
pages = "1-168",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_2774"
}
Jelenković, A.. (2016). Aluminum neurotoxicity: From subtle molecular lesions to neurological diseases. in Aluminum Neurotoxicity: From Subtle Molecular Lesions to Neurological Diseases
Nova Science Publishers, Inc., New York., 1-168.
https://hdl.handle.net/21.15107/rcub_ibiss_2774
Jelenković A. Aluminum neurotoxicity: From subtle molecular lesions to neurological diseases. in Aluminum Neurotoxicity: From Subtle Molecular Lesions to Neurological Diseases. 2016;:1-168.
https://hdl.handle.net/21.15107/rcub_ibiss_2774 .
Jelenković, Ankica, "Aluminum neurotoxicity: From subtle molecular lesions to neurological diseases" in Aluminum Neurotoxicity: From Subtle Molecular Lesions to Neurological Diseases (2016):1-168,
https://hdl.handle.net/21.15107/rcub_ibiss_2774 .
1

The Protective and Dose-Dependent Effects of L-Name in Aluminium-Induced Neurotoxicity

Jelenković, Ankica; Jelenković, Ankica; Jovanović, Marina D.; Petronijević, Nataša; Lepić, Toplica

(Nova Science Publishers, 2016)

TY  - CHAP
AU  - Jelenković, Ankica
AU  - Jovanović, Marina D.
AU  - Petronijević, Nataša
AU  - Lepić, Toplica
PY  - 2016
UR  - https://www.novapublishers.com/catalog/product_info.php?products_id=59851&osCsid=8e6df2fe6f876c8f3f77799c9f9187b2
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/2627
AB  - Numerous research studies have undoubtedly shown that aluminium is a very harmful substance which enters the human body externally from the environment. The aluminum intake usually happens unintentionally, due to the fact that people know little about its prevalence in water, factory-processed foods, medicines, cosmetics, etc. When accumulated in human organs, it can cause severe damage, and even lead to chronic neurodegenerative diseases, including Alzheimer‘s disease. The extent to which nitric oxide (NO) is involved in the basic mechanisms of aluminum neurotoxicity, like oxidative stress and the antioxidant defense, is intriguing scientific community. In this chapter are presented results of the intrahippocampal application of aluminum chloride and a pretreatment with Nω-nitro-L-arginine methyl ester (L-NAME), the non-selective inhibitor of nitric oxide synthase activities. It turned out that, in order to avoid erroneous conclusions about NO not being involved in aluminium-induced neurotoxicity, it was necessary to titrate the dose of L-NAME (1, 10 and 100 micrograms). Among the three doses applied prior to the application of aluminum, only the highest dose acted as an antioxidant in the four examined brain structures.
PB  - Nova Science Publishers
T2  - Aluminum Neurotoxicity: From Subtle Molecular Lesions to Neurological Diseases
T1  - The Protective and Dose-Dependent Effects of L-Name in Aluminium-Induced Neurotoxicity
SP  - 69
EP  - 90
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_2627
ER  - 
@inbook{
editor = "Jelenković, Ankica",
author = "Jelenković, Ankica and Jovanović, Marina D. and Petronijević, Nataša and Lepić, Toplica",
year = "2016",
abstract = "Numerous research studies have undoubtedly shown that aluminium is a very harmful substance which enters the human body externally from the environment. The aluminum intake usually happens unintentionally, due to the fact that people know little about its prevalence in water, factory-processed foods, medicines, cosmetics, etc. When accumulated in human organs, it can cause severe damage, and even lead to chronic neurodegenerative diseases, including Alzheimer‘s disease. The extent to which nitric oxide (NO) is involved in the basic mechanisms of aluminum neurotoxicity, like oxidative stress and the antioxidant defense, is intriguing scientific community. In this chapter are presented results of the intrahippocampal application of aluminum chloride and a pretreatment with Nω-nitro-L-arginine methyl ester (L-NAME), the non-selective inhibitor of nitric oxide synthase activities. It turned out that, in order to avoid erroneous conclusions about NO not being involved in aluminium-induced neurotoxicity, it was necessary to titrate the dose of L-NAME (1, 10 and 100 micrograms). Among the three doses applied prior to the application of aluminum, only the highest dose acted as an antioxidant in the four examined brain structures.",
publisher = "Nova Science Publishers",
journal = "Aluminum Neurotoxicity: From Subtle Molecular Lesions to Neurological Diseases",
booktitle = "The Protective and Dose-Dependent Effects of L-Name in Aluminium-Induced Neurotoxicity",
pages = "69-90",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_2627"
}
Jelenković, A., Jelenković, A., Jovanović, M. D., Petronijević, N.,& Lepić, T.. (2016). The Protective and Dose-Dependent Effects of L-Name in Aluminium-Induced Neurotoxicity. in Aluminum Neurotoxicity: From Subtle Molecular Lesions to Neurological Diseases
Nova Science Publishers., 69-90.
https://hdl.handle.net/21.15107/rcub_ibiss_2627
Jelenković A, Jelenković A, Jovanović MD, Petronijević N, Lepić T. The Protective and Dose-Dependent Effects of L-Name in Aluminium-Induced Neurotoxicity. in Aluminum Neurotoxicity: From Subtle Molecular Lesions to Neurological Diseases. 2016;:69-90.
https://hdl.handle.net/21.15107/rcub_ibiss_2627 .
Jelenković, Ankica, Jelenković, Ankica, Jovanović, Marina D., Petronijević, Nataša, Lepić, Toplica, "The Protective and Dose-Dependent Effects of L-Name in Aluminium-Induced Neurotoxicity" in Aluminum Neurotoxicity: From Subtle Molecular Lesions to Neurological Diseases (2016):69-90,
https://hdl.handle.net/21.15107/rcub_ibiss_2627 .

The protective effects of intrahippocampal application of green tea leaf extract on aluminium-induced brain toxicity

Powell, Nicolas; Jelenković, Ankica; Jovanović, Marina D.; Petronijević, Nataša

(Nova Science Publishers, Inc., New York, 2015)

TY  - CHAP
AU  - Jelenković, Ankica
AU  - Jovanović, Marina D.
AU  - Petronijević, Nataša
PY  - 2015
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/2567
UR  - https://www.novapublishers.com/catalog/product_info.php?products_id=54968
AB  - Diets have attracted great interest on the account of growing evidence of their beneficial effects on human health. Green tea has been used for a very long time as a folk remedy for a wide array of diseases. The well-known green tea beverage is made from a plant Camellia sinensis. The healthy properties of green tea are linked closely to its content of phenolic compounds, particularly to the (-)-epigallocatechin-3-gallate. It has been proposed that green tea may have a beneficial impact on a number of brain functions, as well as on neurodegenerative disorder prevention in humans and in various animal models, including Alzheimer's disease (AD). A large number of scientific studies have supported some of these assumptions. In the case of AD, aluminium may have an important role in the disease aetiology/pathogenesis/precipitation. However, aluminium has biological effects in the green tea plant, where it is a cofactor for polyphenol biosynthesis. Consequently, leaves of green tea accumulate and store large quantities of this element during the plant growth. Thus, it was intriguing whether the unilateral intrahippocampal application of green tea leaf extract (GTLE) and aluminium chloride would have any interaction, measured by the biochemical parameters in six brain structures: the forebrain cortex, striatum, basal forebrain, hippocampus, brain stem and cerebellum, of the adult male Wistar rats. It was found that GTLE given alone demonstrated biochemical effects not only in the ipsilateral hippocampus, but also spread into the five other examined structures at the same side, as well as into the identical brain structures on the contralateral hemisphere. In fact, there were no differences in the activity of superoxide dismutase, cytochrome c oxidase (COX) and acetylcholinesterase (AChE) between the right and the corresponding left brain structures. Moreover, the activity of COX and AChE were significantly higher when compared to the control group. Out of the three observed parameters, the content of reduced glutathione (GSH), superoxide anion and nitrites, aluminium itself demonstrated the strongest effects towards GSH, which was significantly reduced in all structures, compared to the control group. The changes were identical in the ipsi- and contralateral corresponding structures. Howewer, the application of GTLE just before aluminium prevented the reduction of GSH induced by aluminium, and significantly increased its content compared to the control group. Also, the content of superoxide anion was significantly reduced in most structures compared to the control, and to the aluminium-treated group as well. The obtained results of GTE in the aluminium-induced neurotoxicity are in accordance with the antioxidant effects of GTLE. Also, it is clear that GTE administered alone did not demonstrate neurotoxic effects as did the solution of aluminium chloride, but, on the contrary, showed the opposite, neuroprotective effects. To sum up, GTLE has proved to manifest strong antioxidant effects in the brain of healthy rats, and in the cases of neurotoxicity induced by aluminum, as well.
PB  - Nova Science Publishers, Inc., New York
T2  - Green tea and health: antioxidant properties, consumption and role in disease prevention
T1  - The protective effects of intrahippocampal application of green tea leaf extract on aluminium-induced brain toxicity
SP  - 33
EP  - 56
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_2567
ER  - 
@inbook{
editor = "Powell, Nicolas",
author = "Jelenković, Ankica and Jovanović, Marina D. and Petronijević, Nataša",
year = "2015",
abstract = "Diets have attracted great interest on the account of growing evidence of their beneficial effects on human health. Green tea has been used for a very long time as a folk remedy for a wide array of diseases. The well-known green tea beverage is made from a plant Camellia sinensis. The healthy properties of green tea are linked closely to its content of phenolic compounds, particularly to the (-)-epigallocatechin-3-gallate. It has been proposed that green tea may have a beneficial impact on a number of brain functions, as well as on neurodegenerative disorder prevention in humans and in various animal models, including Alzheimer's disease (AD). A large number of scientific studies have supported some of these assumptions. In the case of AD, aluminium may have an important role in the disease aetiology/pathogenesis/precipitation. However, aluminium has biological effects in the green tea plant, where it is a cofactor for polyphenol biosynthesis. Consequently, leaves of green tea accumulate and store large quantities of this element during the plant growth. Thus, it was intriguing whether the unilateral intrahippocampal application of green tea leaf extract (GTLE) and aluminium chloride would have any interaction, measured by the biochemical parameters in six brain structures: the forebrain cortex, striatum, basal forebrain, hippocampus, brain stem and cerebellum, of the adult male Wistar rats. It was found that GTLE given alone demonstrated biochemical effects not only in the ipsilateral hippocampus, but also spread into the five other examined structures at the same side, as well as into the identical brain structures on the contralateral hemisphere. In fact, there were no differences in the activity of superoxide dismutase, cytochrome c oxidase (COX) and acetylcholinesterase (AChE) between the right and the corresponding left brain structures. Moreover, the activity of COX and AChE were significantly higher when compared to the control group. Out of the three observed parameters, the content of reduced glutathione (GSH), superoxide anion and nitrites, aluminium itself demonstrated the strongest effects towards GSH, which was significantly reduced in all structures, compared to the control group. The changes were identical in the ipsi- and contralateral corresponding structures. Howewer, the application of GTLE just before aluminium prevented the reduction of GSH induced by aluminium, and significantly increased its content compared to the control group. Also, the content of superoxide anion was significantly reduced in most structures compared to the control, and to the aluminium-treated group as well. The obtained results of GTE in the aluminium-induced neurotoxicity are in accordance with the antioxidant effects of GTLE. Also, it is clear that GTE administered alone did not demonstrate neurotoxic effects as did the solution of aluminium chloride, but, on the contrary, showed the opposite, neuroprotective effects. To sum up, GTLE has proved to manifest strong antioxidant effects in the brain of healthy rats, and in the cases of neurotoxicity induced by aluminum, as well.",
publisher = "Nova Science Publishers, Inc., New York",
journal = "Green tea and health: antioxidant properties, consumption and role in disease prevention",
booktitle = "The protective effects of intrahippocampal application of green tea leaf extract on aluminium-induced brain toxicity",
pages = "33-56",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_2567"
}
Powell, N., Jelenković, A., Jovanović, M. D.,& Petronijević, N.. (2015). The protective effects of intrahippocampal application of green tea leaf extract on aluminium-induced brain toxicity. in Green tea and health: antioxidant properties, consumption and role in disease prevention
Nova Science Publishers, Inc., New York., 33-56.
https://hdl.handle.net/21.15107/rcub_ibiss_2567
Powell N, Jelenković A, Jovanović MD, Petronijević N. The protective effects of intrahippocampal application of green tea leaf extract on aluminium-induced brain toxicity. in Green tea and health: antioxidant properties, consumption and role in disease prevention. 2015;:33-56.
https://hdl.handle.net/21.15107/rcub_ibiss_2567 .
Powell, Nicolas, Jelenković, Ankica, Jovanović, Marina D., Petronijević, Nataša, "The protective effects of intrahippocampal application of green tea leaf extract on aluminium-induced brain toxicity" in Green tea and health: antioxidant properties, consumption and role in disease prevention (2015):33-56,
https://hdl.handle.net/21.15107/rcub_ibiss_2567 .
2

The use of green tea in treating obesity

Powell, Nicolas; Jelenković, Ankica; Šumarac Dumanović, Mirjana

(Nova Science Publishers, Inc., New York, 2015)

TY  - CHAP
AU  - Jelenković, Ankica
AU  - Šumarac Dumanović, Mirjana
PY  - 2015
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/2568
UR  - https://www.novapublishers.com/catalog/product_info.php?products_id=54968
AB  - Obesity has been increasing at an alarming rate in the last several decades, both in developed and in developing countries, reaching epidemic proportions among young people and adults as well. Unfortunately, nowadays obesity has become a global health problem. It raises the risk of morbidity from a great number of diseases like: diabetes mellitus Type 2, dyslipidemia, arterial hypertension, coronary heart disease, stroke, cancer and respiratory problems including sleep apnea, etc. Both the direct and indirect costs of obesity and obesity-related morbidity have strong economic impact on the whole society. Therefore, the prevention and treatment of obesity remain and should be a priority worldwide. Besides other possible ways of treatment, phytotherapy has an important role in both scientific research and traditional medicine as well. Green tea beverage made from the dried, non-fermented leaves of the plant Camellia sinensis, has been consumed by humans for thousands of years. It has attained high reputation as a health promoting herb. The increasing interest in the effects of green tea is directed towards its ingredients: catechins, caffeine and theanine, all of which possess various biologically and pharmacologically effects. Some of these compounds are highly attractive in drug discovery programs. It is traditionally thought that green tea consumption decreases the risks for obesity, reduces body weight and helps in treating overweight patients. Consequently, health abnormalities related to obesity may be alleviated by green tea consumption. A number of extensive experimental research and epidemiological studies supported the anti-obesity effects of green tea and its various forms, and proposed very complicated mechanisms concerning its potential influence on the body weight and composition. At least, the modulation of lipid and carbohydrate metabolism, body energy balance and food intake could be obtain by consuming green tea. Its antioxidant effects in treating obesity are also exploited. Green tea and its commercial forms (which generally contain ingredients like catechins and caffeine in a higher concentration than the typical green tea beverage) have proved to be highly successful in controlled experiments, but they did not demonstrate identical and unambiguous effects in randomised clinical trials (RCTs). That is the reason why its safety and efficacy could not be properly judged and claimed to be a complementary and alternative medicine used to aid weight loss and weight maintenance. To overcome the problem of the insufficient number of RCTs, a lot of systematic reviews and meta-analyses have been conducted. However, in spite of some benefits shown in decreasing body weight and weight maintenance, the obtained improvement, in general, did not reach statistical significance. That could be the result of great heterogeneity of these trials. Thus, well-characterised, randomised controlled clinical trials are needed in order to assess the promising effects of different forms of green tea on health promotion in overweight and obese humans. In order to avoid possible misleading and aggressive commercial practices conducted by the advertisers, such reliable information is extraordinary important for health-care workers, and for green tea consumers as well.
PB  - Nova Science Publishers, Inc., New York
T2  - Green tea and health: antioxidant properties, consumption and role in disease prevention
T1  - The use of green tea in treating obesity
SP  - 115
EP  - 135
EP  - Jelenković, A., & Šumarac Dumanović, M. (2015). The use of green tea in treating obesity. In N. Powell (Ed.), Green tea and health: antioxidant properties, consumption and role in disease prevention, Food and Beverage Consumption and Health (pp. 115–135). New York: Nova Science Publishers, Inc.
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_2568
ER  - 
@inbook{
editor = "Powell, Nicolas",
author = "Jelenković, Ankica and Šumarac Dumanović, Mirjana",
year = "2015",
abstract = "Obesity has been increasing at an alarming rate in the last several decades, both in developed and in developing countries, reaching epidemic proportions among young people and adults as well. Unfortunately, nowadays obesity has become a global health problem. It raises the risk of morbidity from a great number of diseases like: diabetes mellitus Type 2, dyslipidemia, arterial hypertension, coronary heart disease, stroke, cancer and respiratory problems including sleep apnea, etc. Both the direct and indirect costs of obesity and obesity-related morbidity have strong economic impact on the whole society. Therefore, the prevention and treatment of obesity remain and should be a priority worldwide. Besides other possible ways of treatment, phytotherapy has an important role in both scientific research and traditional medicine as well. Green tea beverage made from the dried, non-fermented leaves of the plant Camellia sinensis, has been consumed by humans for thousands of years. It has attained high reputation as a health promoting herb. The increasing interest in the effects of green tea is directed towards its ingredients: catechins, caffeine and theanine, all of which possess various biologically and pharmacologically effects. Some of these compounds are highly attractive in drug discovery programs. It is traditionally thought that green tea consumption decreases the risks for obesity, reduces body weight and helps in treating overweight patients. Consequently, health abnormalities related to obesity may be alleviated by green tea consumption. A number of extensive experimental research and epidemiological studies supported the anti-obesity effects of green tea and its various forms, and proposed very complicated mechanisms concerning its potential influence on the body weight and composition. At least, the modulation of lipid and carbohydrate metabolism, body energy balance and food intake could be obtain by consuming green tea. Its antioxidant effects in treating obesity are also exploited. Green tea and its commercial forms (which generally contain ingredients like catechins and caffeine in a higher concentration than the typical green tea beverage) have proved to be highly successful in controlled experiments, but they did not demonstrate identical and unambiguous effects in randomised clinical trials (RCTs). That is the reason why its safety and efficacy could not be properly judged and claimed to be a complementary and alternative medicine used to aid weight loss and weight maintenance. To overcome the problem of the insufficient number of RCTs, a lot of systematic reviews and meta-analyses have been conducted. However, in spite of some benefits shown in decreasing body weight and weight maintenance, the obtained improvement, in general, did not reach statistical significance. That could be the result of great heterogeneity of these trials. Thus, well-characterised, randomised controlled clinical trials are needed in order to assess the promising effects of different forms of green tea on health promotion in overweight and obese humans. In order to avoid possible misleading and aggressive commercial practices conducted by the advertisers, such reliable information is extraordinary important for health-care workers, and for green tea consumers as well.",
publisher = "Nova Science Publishers, Inc., New York",
journal = "Green tea and health: antioxidant properties, consumption and role in disease prevention",
booktitle = "The use of green tea in treating obesity",
pages = "115-135-Jelenković, A., & Šumarac Dumanović, M. (2015). The use of green tea in treating obesity. In N. Powell (Ed.), Green tea and health: antioxidant properties, consumption and role in disease prevention, Food and Beverage Consumption and Health (pp. 115–135). New York: Nova Science Publishers, Inc.",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_2568"
}
Powell, N., Jelenković, A.,& Šumarac Dumanović, M.. (2015). The use of green tea in treating obesity. in Green tea and health: antioxidant properties, consumption and role in disease prevention
Nova Science Publishers, Inc., New York., 115-135.
https://hdl.handle.net/21.15107/rcub_ibiss_2568
Powell N, Jelenković A, Šumarac Dumanović M. The use of green tea in treating obesity. in Green tea and health: antioxidant properties, consumption and role in disease prevention. 2015;:115-135.
https://hdl.handle.net/21.15107/rcub_ibiss_2568 .
Powell, Nicolas, Jelenković, Ankica, Šumarac Dumanović, Mirjana, "The use of green tea in treating obesity" in Green tea and health: antioxidant properties, consumption and role in disease prevention (2015):115-135,
https://hdl.handle.net/21.15107/rcub_ibiss_2568 .

Different effects of chronic exposure to ELF magnetic field on spontaneous and amphetamine-induced locomotor and stereotypic activities in rats

Petković, Branka; Pešić, Vesna; Jelenković, Ankica; Vorobyov, Vasily; Prolić, Zlatko

(Pergamon-Elsevier Science Ltd, 2005)

TY  - JOUR
AU  - Petković, Branka
AU  - Pešić, Vesna
AU  - Jelenković, Ankica
AU  - Vorobyov, Vasily
AU  - Prolić, Zlatko
PY  - 2005
UR  - https://www.sciencedirect.com/science/article/abs/pii/S0361923005003011?via%3Dihub
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3807
AB  - The effects of chronic (7 days) exposure to an extremely low frequency magnetic field (ELF-MF, 50 Hz, 0.5 mT) on spontaneous and amphetamine-induced (1.5 mg/kg, i.p.) locomotor and stereotypic activities in adult rats were examined by open field test for 2 h on exposure days 1, 3, and 7. After 1 day of exposure to ELF-MF, the spontaneous locomotor activity was increased clearly at the first hour of observation and significantly at the second one as compared to the corresponding values in other series with ELF-MF and sham-exposed animals. After 7 days of exposure to ELF-MF, an amphetamine enhancing effect on the locomotor activity was significantly reduced at the second hour of observation as compared to that in 1-day- and sham-exposed rats treated with amphetamine. In contrast to the locomotor activity, the amphetamine-induced stereotypic behaviour in 7-day pre-exposed rats was significantly reduced at the first hour versus sham-exposed rats. While at the second hour of observation this effect was significant as compared to 1- and 3-day exposed animals (but not sham-exposed rats). Our results indicate that an extremely low frequency magnetic field is able to affect differently two types of behaviour, which are dependent on both the time course of exposure and the imbalance in the brain mediatory systems.
PB  - Pergamon-Elsevier Science Ltd
T2  - Brain Research Bulletin
T1  - Different effects of chronic exposure to ELF magnetic field on spontaneous and amphetamine-induced locomotor and stereotypic activities in rats
IS  - 6
VL  - 67
DO  - 10.1016/j.brainresbull.2005.07.017
SP  - 498
EP  - 503
ER  - 
@article{
author = "Petković, Branka and Pešić, Vesna and Jelenković, Ankica and Vorobyov, Vasily and Prolić, Zlatko",
year = "2005",
abstract = "The effects of chronic (7 days) exposure to an extremely low frequency magnetic field (ELF-MF, 50 Hz, 0.5 mT) on spontaneous and amphetamine-induced (1.5 mg/kg, i.p.) locomotor and stereotypic activities in adult rats were examined by open field test for 2 h on exposure days 1, 3, and 7. After 1 day of exposure to ELF-MF, the spontaneous locomotor activity was increased clearly at the first hour of observation and significantly at the second one as compared to the corresponding values in other series with ELF-MF and sham-exposed animals. After 7 days of exposure to ELF-MF, an amphetamine enhancing effect on the locomotor activity was significantly reduced at the second hour of observation as compared to that in 1-day- and sham-exposed rats treated with amphetamine. In contrast to the locomotor activity, the amphetamine-induced stereotypic behaviour in 7-day pre-exposed rats was significantly reduced at the first hour versus sham-exposed rats. While at the second hour of observation this effect was significant as compared to 1- and 3-day exposed animals (but not sham-exposed rats). Our results indicate that an extremely low frequency magnetic field is able to affect differently two types of behaviour, which are dependent on both the time course of exposure and the imbalance in the brain mediatory systems.",
publisher = "Pergamon-Elsevier Science Ltd",
journal = "Brain Research Bulletin",
title = "Different effects of chronic exposure to ELF magnetic field on spontaneous and amphetamine-induced locomotor and stereotypic activities in rats",
number = "6",
volume = "67",
doi = "10.1016/j.brainresbull.2005.07.017",
pages = "498-503"
}
Petković, B., Pešić, V., Jelenković, A., Vorobyov, V.,& Prolić, Z.. (2005). Different effects of chronic exposure to ELF magnetic field on spontaneous and amphetamine-induced locomotor and stereotypic activities in rats. in Brain Research Bulletin
Pergamon-Elsevier Science Ltd., 67(6), 498-503.
https://doi.org/10.1016/j.brainresbull.2005.07.017
Petković B, Pešić V, Jelenković A, Vorobyov V, Prolić Z. Different effects of chronic exposure to ELF magnetic field on spontaneous and amphetamine-induced locomotor and stereotypic activities in rats. in Brain Research Bulletin. 2005;67(6):498-503.
doi:10.1016/j.brainresbull.2005.07.017 .
Petković, Branka, Pešić, Vesna, Jelenković, Ankica, Vorobyov, Vasily, Prolić, Zlatko, "Different effects of chronic exposure to ELF magnetic field on spontaneous and amphetamine-induced locomotor and stereotypic activities in rats" in Brain Research Bulletin, 67, no. 6 (2005):498-503,
https://doi.org/10.1016/j.brainresbull.2005.07.017 . .
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Non-linearity in combined effects of ELF magnetic field and amphetamine on motor activity in rats

Pešić, Vesna; Petković, Branka; Jelenković, Ankica; Vorobyov, Vasily; Prolić, Zlatko

(Elsevier, 2004)

TY  - JOUR
AU  - Pešić, Vesna
AU  - Petković, Branka
AU  - Jelenković, Ankica
AU  - Vorobyov, Vasily
AU  - Prolić, Zlatko
PY  - 2004
UR  - https://www.sciencedirect.com/science/article/pii/S016643280300281X?via%3Dihub
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3810
AB  - The effects of short-term (15 min) pre-exposure of rats to extremely low-frequency magnetic field (ELF-MF, 50 Hz, 6 mT) on their motor (locomotor and stereotypic) activity induced by D-amphetamine sulphate (AMPH) at different doses (0.5, 1.5 and 4.5 mg/kg, i.p.) were studied in the open field test. In saline-treated rats both parameters of motor activity were unaffected by ELF-MF irradiation. The rats pre-exposed to ELF-MF and injected with the lowest dose of AMPH showed the same locomotor activity as control animals, while their stereotypic behaviour was significantly elevated. ELF-MF in combination with AMPH at higher doses significantly enhanced motor activity when compared with values obtained in both control and combined experiments with the lowest dose of the drug. However, only combined locomotor effect at the middle dose of AMPH was significantly greater than those observed in corresponding experiments with AMPH alone. These results demonstrate that acute short-term exposure to ELF-MF is able to modify a motor activity in dependence on the extent of AMPH-induced neurotransmitter imbalance.
PB  - Elsevier
T2  - Behavioural Brain Research
T1  - Non-linearity in combined effects of ELF magnetic field and amphetamine on motor activity in rats
IS  - 1-2
VL  - 150
DO  - 10.1016/j.bbr.2003.07.003
SP  - 223
EP  - 227
ER  - 
@article{
author = "Pešić, Vesna and Petković, Branka and Jelenković, Ankica and Vorobyov, Vasily and Prolić, Zlatko",
year = "2004",
abstract = "The effects of short-term (15 min) pre-exposure of rats to extremely low-frequency magnetic field (ELF-MF, 50 Hz, 6 mT) on their motor (locomotor and stereotypic) activity induced by D-amphetamine sulphate (AMPH) at different doses (0.5, 1.5 and 4.5 mg/kg, i.p.) were studied in the open field test. In saline-treated rats both parameters of motor activity were unaffected by ELF-MF irradiation. The rats pre-exposed to ELF-MF and injected with the lowest dose of AMPH showed the same locomotor activity as control animals, while their stereotypic behaviour was significantly elevated. ELF-MF in combination with AMPH at higher doses significantly enhanced motor activity when compared with values obtained in both control and combined experiments with the lowest dose of the drug. However, only combined locomotor effect at the middle dose of AMPH was significantly greater than those observed in corresponding experiments with AMPH alone. These results demonstrate that acute short-term exposure to ELF-MF is able to modify a motor activity in dependence on the extent of AMPH-induced neurotransmitter imbalance.",
publisher = "Elsevier",
journal = "Behavioural Brain Research",
title = "Non-linearity in combined effects of ELF magnetic field and amphetamine on motor activity in rats",
number = "1-2",
volume = "150",
doi = "10.1016/j.bbr.2003.07.003",
pages = "223-227"
}
Pešić, V., Petković, B., Jelenković, A., Vorobyov, V.,& Prolić, Z.. (2004). Non-linearity in combined effects of ELF magnetic field and amphetamine on motor activity in rats. in Behavioural Brain Research
Elsevier., 150(1-2), 223-227.
https://doi.org/10.1016/j.bbr.2003.07.003
Pešić V, Petković B, Jelenković A, Vorobyov V, Prolić Z. Non-linearity in combined effects of ELF magnetic field and amphetamine on motor activity in rats. in Behavioural Brain Research. 2004;150(1-2):223-227.
doi:10.1016/j.bbr.2003.07.003 .
Pešić, Vesna, Petković, Branka, Jelenković, Ankica, Vorobyov, Vasily, Prolić, Zlatko, "Non-linearity in combined effects of ELF magnetic field and amphetamine on motor activity in rats" in Behavioural Brain Research, 150, no. 1-2 (2004):223-227,
https://doi.org/10.1016/j.bbr.2003.07.003 . .
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