Panax ginseng ginsenoside-Rg₂ protects memory impairment via anti-apoptosis in a rat model with vascular dementia
Ethnopharmacological relevance: Ginsenosides, the major active ingredients of Panax ginseng, produce a variety of pharmacological or physiological responses with effects on the central and peripheral nervous systems. Aim of the Study: In this report, we investigated the effects of ginsenoside Rg₂ on...
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Published in | Journal of ethnopharmacology Vol. 115; no. 3; pp. 441 - 448 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Shannon
Amsterdam; New York: Elsevier
12.02.2008
Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 0378-8741 1872-7573 |
DOI | 10.1016/j.jep.2007.10.026 |
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Summary: | Ethnopharmacological relevance: Ginsenosides, the major active ingredients of Panax ginseng, produce a variety of pharmacological or physiological responses with effects on the central and peripheral nervous systems. Aim of the Study: In this report, we investigated the effects of ginsenoside Rg₂ on cerebral ischemia-reperfusion induced impairment of neurological responses, memory and caudate-putamen neuronal apoptosis in a vascular dementia (VD) rat model. Materials and Methods: Neurological evaluation was performed 24h after reperfusion and Y-maze memory performance was assessed at 48h after reperfusion. Immunocytochemical techniques were employed to check the protein expression of BCL-2, BAX, heat shock protein 70 and P53, which are related with cell apoptosis. Results: Neurological responses and memory ability of the ginsenoside Rg₂ or nimodipine groups improved significantly compared with the VD group. The expression of BCL-2 and HSP70 were decreased, while BAX and P53 were increased in the VD model. The expression of BCL-2 and HSP70 proteins were increased, while BAX and P53 decreased after ginsenoside Rg₂ (2.5, 5 and 10mg/kg) and nimodipine (50μg/kg) treatment compared with the VD group. The study suggests that ginsenoside Rg₂ improved neurological performance and memory ability of VD rats through mechanisms related to anti-apoptosis. Conclusions: The capacity for ginsenoside Rg₂ to modulate the expression of apoptotic related proteins suggests that ginsenoside Rg₂ may represent a potential treatment strategy for vascular dementia or other ischemic insults. |
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Bibliography: | http://dx.doi.org/10.1016/j.jep.2007.10.026 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 0378-8741 1872-7573 |
DOI: | 10.1016/j.jep.2007.10.026 |