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Journal of Chinese Pharmaceutical Sciences ›› 2020, Vol. 29 ›› Issue (12): 880-895.DOI: 10.5246/jcps.2020.12.078

• Original articles • Previous Articles     Next Articles

Protective effect of hydroxysafflor yellow A on Parkinson cell model and its network pharmacology analysis

Shuang Li1,3, Chunyan Guo1,2,*(), Shuangshuang Li1, Sihan You1, Xiujuan Yu1   

  1. 1 Department of Pharmacy, HeBei North University, Zhangjiakou 075000, China
    2 Hebei Key Laboratory of Neuropharmacology, Zhangjiakou 075000, China
    3 College of Life Sciences, Hebei Normal University, Shijiazhuang 050024, China
  • Received:2020-09-15 Revised:2020-10-20 Accepted:2020-11-01 Online:2020-12-30 Published:2020-12-30
  • Contact: Chunyan Guo
  • About author:
    Chunyan Guo, Ph.D., Professor of Chemistry of Hebei North University, Supervisor of Master Students, is currently the member of Science and Technology Branch of Academic Committee. Dr. Guo is also the Executive Director of Hebei Pharmacology Society. In 2012, Dr. Guo went to University of Manitoba as a visiting scholar. Dr. Guo's main research direction includes analysis of active components and its derived metabolites of medicinal natural products in vivo. She held Science and Technology Support Plan Projects of Hebei Province, and has won the third prize of Science and Technology Progress of Hebei Province. At present, she mainly undertakes the teaching works of Analytical Chemistry, Pharmaceutical Analysis, Biopharmaceutical Analysis and Drug Quality Testing Technology.

Abstract:

As an effective component of safflower, hydroxysafflor yellow A (HSYA) has the effect of promoting blood circulation, removing blood stasis, and relieving pain, and it has a certain effect on blood stasis and wind-induced Parkinson’s disease (PD). However, the current research mostly involves a single intervention mechanism, which is not conducive to the clinical transformation of this type of drugs. In the present study, rotenone was used to construct a PD cell model, and the protective effect of HSYA on the PD cell model was evaluated by cell viability and mitochondrial membrane potential. TTD database was used to query PD-related therapeutic targets, Swiss Target Prediction database to query HSYA-related targets, STRING database was used to search the gene interaction relationship of common targets, and ClueGO pathway was adopted to enrich and analyze common targets and their interaction targets, as well as to explore the comprehensive intervention mechanism. The results showed that rotenone could successfully establish the PD cell model, and HSYA had significant protective effect on PD cell model. Through the network pharmacological analysis, 36 PD-related therapeutic targets and 88 HSYA-related targets were queried. The common targets of PD and HSYA were FKBP1A, HTR1A, SLC6A4 and SLC6A3. To enrich four common targets and their interaction targets through REACTOME pathway, eight cell signal pathways were obtained, and six cell biological processes were obtained through biological process pathway enrichment.

Key words: Hydroxysafflor yellow A, Parkinson's disease, Network pharmacology

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