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Cerebroprotective activity of on global cerebral ischemia in rats. | LitMetric

Cerebroprotective activity of on global cerebral ischemia in rats.

Indian J Pharmacol

Department of Chemistry, Chalapathi Institute of Pharmaceutical Sciences, Guntur, Andhra Pradesh, India.

Published: June 2017

Objectives: The study was performed to evaluate the cerebroprotective activity of methanolic extract (ME) of - a folk medicine used as anti-inflammatory and in central nervous system ailments. It has high phenolic and flavonoid contents including rutin.

Materials And Methods: Global cerebral ischemia was induced in male albino Wistar rats by temporary bilateral carotid artery occlusion (BCAO) for 30 min, followed by 4 h reperfusion. Groups of rats were pretreated for 10 days with 100, 200, and 400 mg/kg of ME of and 3 mg/kg of edaravone, a marketed cerebroprotective agent, as standard. Antioxidant enzymes such as, the levels of malondialdehyde (MDA), glutathione peroxidase (GPx), glutathione reductase (GR), glutathione-S-transferase (GST), superoxide dismutase (SOD), catalase (CAT) and hydrogen peroxide (HO), protein content, brain water content, cerebral infarct size and the histopathological changes were measured.

Results: -pretreated groups restored the biochemical parameters significantly in a dose-dependent manner. The ischemic changes were involved with an increase in the concentration of MDA and HO, followed by decreased SOD, CAT, GPx, GR, and GST activity in rat brain. The neurodegenaration and its attenuation by were confirmed by examination of triphenyl tetrazolium chloride staining and histopathological changes in the cerebral ischemic rat brains. Similarly, reversed the brain water content in the ischemia-reperfusion animals.

Conclusion: The result of the study indicates that the treatment with enhances the antioxidant defense against BCAO-induced global cerebral ischemia/reperfusion and exerts cerebroprotection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155472PMC
http://dx.doi.org/10.4103/0253-7613.194849DOI Listing

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