Neuroprotective effects of Ginkgo biloba dropping pills in Parkinson's disease

被引:37
|
作者
Yu, Dingyi [1 ]
Zhang, Pengli [1 ]
Li, Junying [1 ]
Liu, Ting [1 ]
Zhang, Yaodan [2 ]
Wang, Qingqing [2 ]
Zhang, Jianbing [2 ]
Lu, Xiaoyan [1 ]
Fan, Xiaohui [1 ]
机构
[1] Zhejiang Univ, Coll Pharmaceut Sci, Pharmaceut Informat Inst, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ Wanbangde Pharmaceut Grp Joint Res, Hangzhou 310058, Zhejiang, Peoples R China
关键词
Ginkgo biloba dropping pills; Parkinson's disease; Neuroprotection; Akt/GSK3; beta; Bax/bcl-2; GLYCOGEN-SYNTHASE KINASE-3; MITOCHONDRIAL DYSFUNCTION; TERPENE TRILACTONES; ALZHEIMERS-DISEASE; MASS-SPECTROMETRY; UPDATE TREATMENTS; OXIDATIVE STRESS; CELL APOPTOSIS; EXTRACT; PLASMA;
D O I
10.1016/j.jpha.2020.06.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Parkinson's disease (PD) is the second most common neurodegenerative disease in the world; however, it lacks effective and safe treatments. Ginkgo biloba dropping pill (GBDP), a unique Chinese G. biloba leaf extract preparation, exhibits antioxidant and neuroprotective effects and has a potential as an alternative therapy for PD. Thus, the aims of this study were to evaluate the effects of GBDP in in vitro and in vivo PD models and to compare the chemical constituents and pharmacological activities of GBDP and the G. biloba extract EGb 761. Using liquid chromatography tandem-mass spectrometry, 46 GBDP constituents were identified. Principal component analysis identified differences in the chemical profiles of GBDP and EGb 761. A quantitative analysis of 12 constituents showed that GBDP had higher levels of several flavonoids and terpene trilactones than EGb 761, whereas EGb 761 had higher levels of organic acids. Moreover, we found that GBDP prevented 6-hydroxydopamine-induced dopaminergic neuron loss in zebrafish and improved cognitive impairment and neuronal damage in methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced PD mice. Although similar effects were observed after EGb 761 treatment, the neuroprotective effects were greater after GBDP treatment on several endpoints. In addition, in vitro results suggested that the Akt/GSK3 beta pathway may be involved in the neuroprotective effects of GBDP. These findings demonstrated that GBDP have potential neuroprotective effects in the treatment of PD. (C) 2020 Xi'an Jiaotong University. Production and hosting by Elsevier B.V.
引用
收藏
页码:220 / 231
页数:12
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