4.7 Article

Danggui-Shaoyao-San ameliorates cognition deficits and attenuates oxidative stress-related neuronal apoptosis in D-galactose-induced senescent mice

期刊

JOURNAL OF ETHNOPHARMACOLOGY
卷 141, 期 1, 页码 386-395

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2012.02.050

关键词

Danggui-Shaoyao-San; D-Galactose; Oxidative stress; Neuronal apoptosis

资金

  1. National Key Scientific and Technological Special Projects [2009ZX09502-011]
  2. Jiangsu Province Program for Culture and Creation Project [CXLX11_0815, CX11B-007XS]
  3. Priority Academic Program Development of Jiangsu Higher Education Institutions

向作者/读者索取更多资源

Ethnopharmacological relevance: Danggui-Shaoyao-San (DSS), a famous traditional Chinese medicine formula consisting of six herbal medicines, has been used to treat gynecological disorders and neural dysfunctions. Aim of the study: The present study was carried out to investigate the effects of DSS on cognitive ability and oxidative stress-related neuronal apoptosis in the hippocampus of aging mice induced by D-galactose (D-gal) to elucidate the underlying molecular mechanisms. Materials and methods: Ethanol extract of DSS (DE) were orally administered to D-gal-induced senescent mice for six weeks. The cognitive ability was determined by the methods of step-down type passive avoidance test and Morris water maze test. The activities of superoxide dismutase (SOD) and nitric oxide synthase (NOS), and levels of carbonyl protein (CP), glutathione (GSH), malondialdehyde (MDA) and nitric oxide (NO) were also examined. Furthermore, the expression of apoptotic related proteins in hippocampus of D-gal-treated mice, such as Bcl-2, Bax and caspase-3 proteins, were determined by immunohistochemistry. Results: DE at the doses of 1.8, 3.6 and 7.2 g/kg significantly enhanced the cognitive performances and restored the abnormal activities of SOD and NOS and levels of CP. MDA, GSH and NO induced by D-gal. Moreover, the neural apoptosis in the hippocampus of D-gal-treated mice was improved by DE through regulating the expression of Bcl-2, Bax and caspase-3. Conclusion: These results demonstrate that DE has neuroprotective effects in D-gal-induced senescent mice by ameliorating oxidative stress induced neuronal apoptosis in the brain. (c) 2012 Elsevier Ireland Ltd. All rights reserved.

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