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作 者:LIN Po-li CAO Jun-ling REN Ping CHEN Jia-li CAO Bo-ya HE Ping ZHENG Chang-hui LI Qi-wen WANG Wei ZHANG Jian
机构地区:[1]School of Chinese Materia Medica,Beijing University of Chinese Medicine,Beijing(100029),China [2]Department of Pharmacy,Dongfang Hospital,Beijing University of Chinese Medicine,Beijing(100078),China [3]School of Chinese Medicine,Beijing University of Chinese Medicine,Beijing(100029),China [4]School of Life Sciences,Beijing University of Chinese Medicine,Beijing(100029),China [5]School of Basic Medical Sciences,Guangzhou University of Chinese Medicine,Guangzhou(510006),China [6]Beijing Key Laboratory of TCM Syndrome and Formula,Beijing(100029),China [7]Key Laboratory of Beijing University of Chinese Medicine,Ministry of Education,Beijing(100029),China
出 处:《Chinese Journal of Integrative Medicine》2023年第12期1087-1098,共12页中国结合医学杂志(英文版)
基 金:Supported by the National Natural Science Foundation of China (No.82004095);the Fundamental Research Funds for the Central Universities (No.2021-JYB-XJSJJ031)。
摘 要:Objective:To explore the potential molecular mechanism of tetrahydropalmatine(THP)on acute myocardial ischemia(AMI).Methods:First,the target genes of THP and AMI were collected from SymMap Database,Traditional Chinese Medicine Database and Analysis Platform,and Swiss Target Prediction,respectively.Then,the overlapping target genes between THP and AMI were evaluated for Grene Ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)enrichment analysis and protein-protein interaction network analysis.The binding affinity between the protein and THP was assessed by molecular docking.Finally,the protective effects of THP on AMI model and oxygen and glucose deprivation(OGD)model of H9C2 cardiomyocyte were explored and the expression levels of target genes were detected by RT-qP CR in vivo and in vitro.Results:MMP9,PPARG,PTGS2,SLC6A4,ESR1,JAK2,GSK3B,NOS2 and AR were recognized as hub genes.The KEGG enrichment analysis results revealed that the potential target genes of THP were involved in the regulation of PPAR and hormone pathways.THP improved the cardiac function,as well as alleviated myocardial cell damage.Furthermore,THP significantly decreased the RNA expression levels of MMP9,PTGS2,SLC6A4,GSK3B and ESR1(P<0.05,P<0.01)after AMI.In vitro,THP significantly increased H9C2 cardiomyocyte viability(P<0.05,P<0.01)and inhibited the RNA expression levels of PPARG,ESR1 and AR(P<0.05,P<0.01)in OGD model.Conclusions:THP could improve cardiac function and alleviate myocardial injury in AMI.The underlying mechanism may be inhibition of inflammation,the improvement of energy metabolism and the regulation of hormones.
关 键 词:TETRAHYDROPALMATINE acute myocardial infarction INFLAMMATION energy metabolism HORMONE
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