1.Chronic Administration of Bacopa Monniera Increases BDNF Protein and mRNA Expressions: A Study in Chronic Unpredictable Stress Induced Animal Model of Depression.
Ritabrata BANERJEE ; Somoday HAZRA ; Anup Kumar GHOSH ; Amal Chandra MONDAL
Psychiatry Investigation 2014;11(3):297-306
OBJECTIVE: The present study aimed to investigate whether graded doses of Bacopa Monniera (BM) extract could produce antidepressant-like effects in chronic unpredictable stress (CUS) induced depression in rats and its possible mechanism(s). METHODS: Rats were subjected to an experimental setting of CUS. The effect of BM extract treatment in CUS-induced depression was examined using behavioral tests including the sucrose consumption, open field test and shuttle box escape test. The mechanism underlying the antidepressant-like action of BM extract was examined by measuring brain-derived neurotrophic factor (BDNF) protein and mRNA expression in brain tissues of CUS-exposed rats. RESULTS: Exposure to CUS for 4 weeks caused depression-like behavior in rats, as indicated by significant decreases in sucrose consumption, locomotor activity and escape latency. In addition, it was found that BDNF protein and mRNA levels in the hippocampus and frontal cortex were lower in CUS-treated rats, as compared to controls. Daily administration of the graded doses of BM extract during the 4-week period of CUS significantly suppressed behavioral changes and attenuated the CUS-induced decrease in BDNF protein and mRNA levels in the hippocampus and frontal cortex. CONCLUSION: The results suggest that BM extract alleviates depression induced by CUS. Present study also confirms that 80-120 mg/kg doses of BM extract have significantly higher antidepressant-like activity.
Animals
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Bacopa*
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Brain
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Brain-Derived Neurotrophic Factor*
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Depression*
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Hippocampus
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Models, Animal*
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Motor Activity
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Rats
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RNA, Messenger*
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Sucrose
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United Nations
2.Elevated level of carbonyl compounds correlates with insulin resistance in type 2 diabetes.
Pinaki SARKAR ; Kaushik KAR ; Mohan Chandra MONDAL ; Indrani CHAKRABORTY ; Manoj KAR
Annals of the Academy of Medicine, Singapore 2010;39(12):909-904
INTRODUCTIONRecent periodicals direct that reactive carbonyl compounds are formed due to existing oxidative stress in type 2 diabetes mellitus, which further nonenzymatically react with proteins and lipids to form irreversible advanced glycation end products (AGE) and advanced lipoxidation end products (ALE). In type 2 diabetes mellitus, insulin resistance plays a pivotal role in hyperglycaemia. In this study, we tried to fi nd the relation between insulin resistance and carbonyl stress.
MATERIALS AND METHODSForty-seven patients of type 2 diabetes mellitus (age 51 ± 5.06 years) were selected and fasting plasma glucose, serum insulin, total carbonyl compounds, HbA1c, thiobarbituric acid reacting substances (TBARS) and Trolox equivalent antioxidant capacity (TEAC) were estimated using standard protocols. Homeostatic model assessement of insulin resistance (HOMA-IR) was evaluated from fasting plasma glucose and serum insulin levels.
RESULTSWe found highly significant correlations of carbonyl compounds with HOMA-IR, fasting plasma glucose and glycated haemoglobin (HbA1c). Correlations of lipid peroxidation end product, TBARS were not so significant.
CONCLUSIONFindings from this study indicate that the level of carbonyl compounds can be a biomarker of insulin resistance in type 2 diabetes mellitus.
Blood Glucose ; metabolism ; Diabetes Mellitus, Type 2 ; metabolism ; physiopathology ; Female ; Glycation End Products, Advanced ; blood ; metabolism ; Homeostasis ; physiology ; Humans ; Hyperglycemia ; metabolism ; Insulin Resistance ; physiology ; Male ; Middle Aged ; Oxidative Stress ; physiology