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Neuroprotective activity of Cymbopogon martinii against cerebral ischemia/reperfusion-induced oxidative stress in rats

Author:
Buch, Prakruti, Patel, Vishal, Ranpariya, Vishavas, Sheth, Navin, Parmar, Sachin
Source:
Journal of ethnopharmacology 2012 v.142 no.1 pp. 35-40
ISSN:
0378-8741
Subject:
Cymbopogon martinii, albino, anorexia, brain, brain damage, carotid arteries, catalase, essential oils, glutathione, histopathology, ischemia, lipid peroxidation, neuroprotective effect, oxidative stress, rats, stroke, superoxide dismutase, thiols
Abstract:
ETHNOPHARMACOLOGICAL RELEVANCE: Cymbopogon martinii (Roxb.) Watson (Family: Graminae), commonly known as Palmarosa, is traditionally prescribed for central nervous system (CNS) disorders such as neuralgia, epileptic fits and anorexia. Although the plant possesses diverse pharmacological actions, the neuroprotective action has got little attention. AIM OF THE STUDY: The present study evaluated neuroprotective effect of essential oil of Cymbopogon martinii (EOCM) against global cerebral ischemia/reperfusion (I/R)-induced oxidative stress in rats. MATERIALS AND METHODS: Global ischemic brain damage was induced by bilateral common carotid artery (BCCA) occlusion for 30min, followed by 60min reperfusion on Wistar albino rats. The biochemical levels of lipid peroxidation (LPO), superoxide dismutase (SOD), catalase (CAT), total thiols and glutathione (GSH) were estimated and brain coronal sections and histopathological studies were performed. RESULTS: BCCA occlusion, followed by reperfusion caused varied biochemical/enzymatic alterations viz. increase in LPO and decrease in SOD, CAT, total thiols and GSH. The prior treatment of EOCM (50mg/kg and 100mg/kg, p.o. for 10 days) markedly reversed these changes and restored to normal levels as compared to I/R groups. Moreover, brain coronal sections and histopathological studies revealed protection against ischemic brain damage in the EOCM-treated groups. CONCLUSION: This study, for the first time, shows potent neuroprotective effect of EOCM against global cerebral I/R-induced oxidative stress in rats, suggesting its therapeutic potential in cerebrovascular diseases (CVD) including stroke.
Agid:
557654