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Ginsenoside Rg3 improves microcystin-induced cardiotoxicity through the miR-128-3p/MDM4 axis

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成果类型:
期刊论文
作者:
Zhou, Xiaoming;Xia, Xiaoyan
通讯作者:
Xia, XY
作者机构:
[Zhou, Xiaoming] Hunan Univ Chinese Med, Hosp 1, Dept Cardiovasc Med, Changsha, Hunan, Peoples R China.
[Xia, Xiaoyan] Changsha Hlth Vocat Coll, Changsha, Hunan, Peoples R China.
[Xia, Xiaoyan; Xia, XY] Xangshan Univ Town, Changsha Hlth Vocat Coll, Acad Affairs Off, 6 Yuening Ave, Changsha 410016, Hunan, Peoples R China.
通讯机构:
[Xia, XY ] X
Xangshan Univ Town, Changsha Hlth Vocat Coll, Acad Affairs Off, 6 Yuening Ave, Changsha 410016, Hunan, Peoples R China.
语种:
英文
关键词:
MDM4;MiR-128-3p;Microcystin;cardiomyocyte toxicity;ginsenoside Rg3
期刊:
Drug and Chemical Toxicology
ISSN:
0148-0545
年:
2023
页码:
1-11
基金类别:
Hunan Natural Science Foundation-Kewei Joint Project 'Discussion and Mechanism Study of Mitochondrial-related miRNAs in Microcystin-mediated Cardiotoxicity and Protective Effects of Ginseng' [2020JJ8094]
机构署名:
本校为第一机构
院系归属:
第一中医临床学院
摘要:
Microcystin (MC) is the byproduct of cyanobacteria metabolism that is associated with oxidative stress and heart damage. This study aimed to investigate the effect of ginsenoside Rg3 on MC-induced cardiotoxicity. A mouse model of myocardial infarction was constructed by oral MC administration. H9C2 cells were used for in vitro analysis. Cellular oxidative stress, apoptosis, and the relationship between miR-128-3p and double minute 4 protein (MDM4) were analyzed. MiR-128-3p expression was upregulated in vitro and in vivo after MC treatment, which was downregulated after Rg3 treatment. Left vent...

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