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Chennam Srinivasulu Shyamaladevi

Researcher at University of Madras

Publications -  16
Citations -  673

Chennam Srinivasulu Shyamaladevi is an academic researcher from University of Madras. The author has contributed to research in topics: Green tea extract & Glutathione. The author has an hindex of 13, co-authored 16 publications receiving 614 citations.

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Therapeutic effect of green tea extract on oxidative stress in aorta and heart of streptozotocin diabetic rats.

TL;DR: Green tea by providing a competent antioxidative mechanism ameliorates the oxidative stress in the aorta and heart of diabetic rats and suggests that green tea may provide a useful therapeutic option in the reversal of oxidative stress induced cardiac dysfunction in diabetes mellitus.
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Green tea extract impedes dyslipidaemia and development of cardiac dysfunction in streptozotocin-diabetic rats.

TL;DR: Green tea can reduce the risk of cardiovascular disease in diabetes with a significant improvement in lipid metabolism and beneficial effects of GTE are ascribed to its antihyperglycaemic and hypolipidaemic activity.
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Green tea impedes dyslipidemia, lipid peroxidation, protein glycation and ameliorates Ca2+ -ATPase and Na+/K+ -ATPase activity in the heart of streptozotocin-diabetic rats.

TL;DR: The data provide support to the therapeutic effect of GTE and suggest that a possible mechanism of action may be associated with the attenuation of the rise in [Ca2+] and [Na+] by ameliorating Ca2+ -ATPase and Na+/K+ - ATPase activities.
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Green tea attenuates diabetes induced Maillard-type fluorescence and collagen cross-linking in the heart of streptozotocin diabetic rats.

TL;DR: The present study reveals that green tea by ameliorating myocardial collagen characteristics may provide a therapeutic option in the treatment of cardiovascular complications of diabetes.
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Effect of Solanum trilobatum on the antioxidant status during diethyl nitrosamine induced and phenobarbital promoted hepatocarcinogenesis in rat.

TL;DR: ST exerts its chemopreventive effects by modulating the antioxidant status during DEN induced hepatocarcinogenesis by modifying the levels of thiobarbituric reactive substances and antioxidant enzymes.