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Yuan-Zhi decoction in the treatment of Alzheimer's disease: An integrated approach based on chemical profiling, network pharmacology, molecular docking and experimental evaluation.
Wu, Qiong; Li, Xiang; Jiang, Xiao-Wen; Yao, Dong; Zhou, Li-Jun; Xu, Zi-Hua; Wang, Nan; Zhao, Qing-Chun; Zhang, Zhou.
Afiliação
  • Wu Q; Department of Life Science and Biochemistry, Shenyang Pharmaceutical University, Shenyang, China.
  • Li X; Department of Pharmacy, General Hospital of Northern Theater Command, Shenyang, China.
  • Jiang XW; Department of Pharmacy, General Hospital of Northern Theater Command, Shenyang, China.
  • Yao D; Department of Life Science and Biochemistry, Shenyang Pharmaceutical University, Shenyang, China.
  • Zhou LJ; Department of Pharmacy, General Hospital of Northern Theater Command, Shenyang, China.
  • Xu ZH; Department of Life Science and Biochemistry, Shenyang Pharmaceutical University, Shenyang, China.
  • Wang N; Department of Pharmacy, General Hospital of Northern Theater Command, Shenyang, China.
  • Zhao QC; Department of Life Science and Biochemistry, Shenyang Pharmaceutical University, Shenyang, China.
  • Zhang Z; Department of Pharmacy, General Hospital of Northern Theater Command, Shenyang, China.
Front Pharmacol ; 13: 893244, 2022.
Article em En | MEDLINE | ID: mdl-36091836
ABSTRACT
Yuan-Zhi Decoction (YZD) is a traditional Chinese medical formulation with demonstrated clinical benefits in Alzheimer's disease (AD). We used liquid chromatography coupled with mass spectrometry to identify 27 unique chemical components of YZD. Analyzing these using network pharmacology and molecular docking models identified 34 potential interacting molecular targets involved in 26 biochemical pathways. When tested in an animal model of AD, the APP/PS1 transgenic mice showed measurable improvements in spatial orientation and memory after the administration of YZD. These improvements coincided with significantly reduced deposition of Aß plaques and tau protein in the hippocampi in the treated animals. In addition, a decreased BACE1 and beta-amyloid levels, a downregulation of the p-GSK-3ß/GSK-3ß, and an upregulation of the PI3K and p-AKT/AKT pathway was seen in YZD treated animals. These in vivo changes validated the involvement of molecular targets and pathways predicted in silico analysis of the chemical components of YZD. This study provides scientific support for the clinical use of YZD and justifies further investigations into its effects in AD. Furthermore, it demonstrates the utility of network pharmacology in elucidating the biochemical mechanisms underlying the beneficial effects of traditional Chinese medicines (TCM).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Pharmacol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Pharmacol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China