Cerebroprotective effects of red ginseng extract pretreatment against ischemia-induced oxidative stress and apoptosis

So Yeong Cheon, Kyoung Joo Cho, Jong Eun Lee, Hyun Woo Kim, Su Kyoung Lee, Hyun Jeong Kim, Gyung Whan Kim

Research output: Contribution to journalArticlepeer-review

15 Citations (Scopus)

Abstract

Panax ginseng C.A. Meyer has been traditionally used as a medicinal plant and has beneficial effects due to pharmacological properties. Although ginseng is thought to be protective under abnormal conditions, the effects of pretreatment with red ginseng (RG) extract on ischemic stroke have not been fully elucidated. We investigated the protective effects of RG extract after focal cerebral ischemia in mice. Crude RG extract (360 mg/kg) was administered intraperitoneally for 2 weeks. Mice were then subjected to occlusion of the middle cerebral artery for 1 hour, followed by reperfusion for 4 and 24 hours. Pretreatment with RG extract followed by ischemia/reperfusion (I/R) resulted in significant reduction of oxidized hydroethidine signals in ischemic areas. At 4 and 24 hours after I/R, the number of 8-hydroxyguanosine and apoptosis signal-regulating kinase 1 (ASK1)-positive cells decreased in the ischemic penumbra as seen using immunofluorescent staining. Western blotting showed that RG efficiently attenuated the protein levels of activated ASK1 in the ischemic penumbra. Consequently, DNA fragmentation and the infarct volume were reduced by RG extract pretreatment 24 hours after I/R. Also, RG extract resulted in better performance in rotarod test after I/R. Thus, RG pretreatment demonstrates a protective effect at suppressing ischemia-induced oxidative stress and apoptosis in ischemic lesions. Pretreatment with crude RG extract may be an effective strategy for preventing brain injury after an ischemic stroke.

Original languageEnglish
Pages (from-to)269-277
Number of pages9
JournalInternational Journal of Neuroscience
Volume123
Issue number4
DOIs
Publication statusPublished - 2013 Apr

Bibliographical note

Funding Information:
The authors report no conflict of interest. The authors alone are responsible for the content and writing of this paper. The financial info needs to be part of the declaration of interests. This study was funded by a grant (A110023) from the Korea Healthcare Technology R&D Project, Ministry of Health & Welfare, Republic of Korea, and supported by the National Research Foundation by the Korea government (NRF 20100012644).

All Science Journal Classification (ASJC) codes

  • Neuroscience(all)

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