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Neuroprotection of ginsenoside Re in cerebral ischemia-reperfusion injury in rats.

Abstract
In the present study, we have investigated the neuroprotective potential of ginsenoside Re (Re) in the middle cerebral artery occlusion model in Sprague-Dawley rats. Adult male Sprague-Dawley rats were treated with Re (5, 10 or 20 mg kg(- 1), P.O. for 7 days, once a day) prior to occlusion. There was a significant increase in the neurological symptoms in ischemic animals as compared with the sham group animals. These effects were attenuated by 10 and 20 mg kg(- 1) Re, P.O. There was a significant increase in the level of malondialdehyde (MDA) in ischemic animals indicating oxidative stress. An elevated level of MDA in ischemic animals was reduced by 10 and 20 mg kg(- 1) Re, P.O., respectively. It was observed that Re significantly decreased mitochondrial swelling, thereby preventing the reduction of H(+)-ATPase activity. This study demonstrates the neuroprotective potential of Re in cerebral ischemia-reperfusion injury in rats.
AuthorsLi-Min Chen, Xiao-Mian Zhou, Ying-Lin Cao, Wen-Xiang Hu
JournalJournal of Asian natural products research (J Asian Nat Prod Res) 2008 May-Jun Vol. 10 Issue 5-6 Pg. 439-45 ISSN: 1028-6020 [Print] England
PMID18464084 (Publication Type: Journal Article)
Chemical References
  • Drugs, Chinese Herbal
  • Ginsenosides
  • Neuroprotective Agents
  • ginsenoside Re
  • Malondialdehyde
  • Proton-Translocating ATPases
Topics
  • Animals
  • Brain Ischemia (drug therapy)
  • Drugs, Chinese Herbal (pharmacology, therapeutic use)
  • Ginsenosides (pharmacology, therapeutic use)
  • Lipid Peroxidation (drug effects)
  • Male
  • Malondialdehyde (metabolism)
  • Mitochondrial Swelling (drug effects)
  • Neuroprotective Agents (pharmacology, therapeutic use)
  • Phytotherapy
  • Proton-Translocating ATPases (metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion Injury (drug therapy)

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