Modified Huang-Lian-Jie-Du Decoction Ameliorates Aβ Synaptotoxicity in a Murine Model of Alzheimer's Disease

被引:44
作者
Liu, Yan [1 ,2 ]
Du, Ting [2 ]
Zhang, Wenlong [1 ]
Lu, Weiye [1 ]
Peng, Zhichao [3 ]
Huang, Shuqiong [2 ]
Sun, Xiangdong [4 ]
Zhu, Xiaoqin [5 ]
Chen, Chaojun [3 ]
Qian, Linchao [2 ]
Wen, Lei [2 ]
Xu, Pingyi [6 ]
Zhang, Yunlong [1 ,7 ]
机构
[1] Guangzhou Med Univ, Sch Basic Med Sci, Key Lab Neurosci, Guangzhou 511436, Guangdong, Peoples R China
[2] Xiamen Univ, Sch Med, Dept Tradit Chinese Med, Xiamen 361102, Fujian, Peoples R China
[3] Guangzhou Chinese Med Integrated Hosp Huadu, Dept Neurol, Guangzhou 510800, Guangdong, Peoples R China
[4] Guangzhou Med Univ, Sch Basic Med Sci, Affiliated Hosp 2, Guangzhou 510260, Guangdong, Peoples R China
[5] Guangzhou Med Univ, Guangzhou 511436, Guangdong, Peoples R China
[6] Guangzhou Med Univ, Dept Neurol, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[7] Xiamen Univ, Shenzhen Res Inst, Shenzhen 518000, Guangdong, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
EXTRACELLULAR ADENOSINE ACCUMULATION; MOUSE MODEL; GUT MICROBIOTA; COGNITIVE IMPAIRMENT; RECEPTORS; NEUROPROTECTION; DYSFUNCTION; INHIBITION; OLIGOMERS; MEMORY;
D O I
10.1155/2019/8340192
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Alzheimer's disease (AD) is a common neurodegenerative disease, characterized by cognitive dysfunction; however, the therapeutic strategies are not fully understood. Huang-Lian-Jie-Du-Decoction (HLJDD) is a famous traditional Chinese herbal formula that has been widely used clinically to treat dementia. Recently, according to previous study and our clinical practice, we generate a new modification of HLJDD (named modified-HLJDD). In this study, we indicated that modified-HLJDD attenuated learning and memory deficiencies in A beta(1-42) oligomer-induced AD model, and we confirmed the exact metabolites in modified-HLJDD solution, as compared with HLJDD by UHPLC-Q-TOF-MS. Using GC-Q-TOF/MS-based metabolomics, we identified adenosine as the potential significant metabolite, responsible for modified-HLJDD regulating energy metabolism and synaptic plasticity in AD model. We also revealed that the potential underlying mechanism of modified-HLJDD in AD model may involve NMDA receptor-mediated glutamatergic transmission and adenosine/ATPase/AMPK cascade. Moreover, we also indicated the differential gut microbiota which mainly involved Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria at the phylum level upon modified-HLJDD treatment in AD model. Based on the correlation of metabolomic analysis with microbiome analysis, we clarified that Dorea is the most affected microbiota with adenosine upon modified-HLJDD treatment in AD model. Thus, our study suggests that modified-HLJDD may serve as a potential therapeutic drug in treating AD.
引用
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页数:27
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