4.7 Article

Neuroprotective effect of SuHeXiang Wan in Drosophila models of Alzheimer's disease

期刊

JOURNAL OF ETHNOPHARMACOLOGY
卷 134, 期 3, 页码 1028-1032

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2011.02.012

关键词

Alzheimer's disease; apoptosis; Drosophila; SuHeXiang Wan; JNK

资金

  1. Ministry for Health & Welfare & Family Affairs, Republic of Korea [B090068]
  2. Korea Health Promotion Institute [B090068] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Aim of the study: SuHeXiang Wan (SHXW) is a Chinese traditional medicinal prescription that consists of 15 crude herbs. SHXW has been used to treat central nervous depression, seizures, infantile convulsion and stroke, and its essential oil has been shown to have anticonvulsant and antioxidative activity. The goal of this study was to investigate the beneficial effects of SHXW on the neurological phenotypes of Drosophila AD models. Materials and methods: We evaluated the effects of a modified SHXW (called KSOP1009) intake on the AD-like phenotypes of Drosophila AD models, which express human A beta 42 in their developing eyes or neurons. Results: When the flies were kept on the media containing 5 mu g/ml of KSOP1009 extract, A beta 42-induced eye degeneration, apoptosis, and the locomotive dysfunctions were strongly suppressed. However. A beta 42 fibril deposits in the A beta 42 overexpressing model were not affected by treatment with KSOP1009 extract. Conversely, KSOP1009 extract intake significantly suppressed the constitutive active form of hemipterous, a JNK activator, while it induced eye degeneration and JNK activation, which has been recognized as an important mediator of A beta 42-associated neuro-cytotoxicity. Conclusions: In conclusion, the results of this study suggest that KSOP1009 confers a therapeutic potential to AD-like pathology of A beta 42 overexpressing Drosophila model via suppression of the hyperactivation of JNK activity and apoptosis. (C) 2011 Elsevier Ireland Ltd. All rights reserved.

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