Lin Yang, Chun-Feng Cheng, Zhi-Fang Li, Xiao-Jing Huang, Shao-Qing Cai, Shan-Yu Ye, Li-Jun Zhao, Yi Xiong, Dong-Feng Chen, He-Lu Liu, Zhen-Xing Ren, Hong-Cheng Fang
International journal of molecular medicine 2023 JunDiabetic cardiomyopathy (DCM) is a cardiovascular disease which has been reported as a major cause of mortality worldwide for several years. Berberine (BBR) is a natural compound extracted from a Chinese herb, with a clinically reported anti‑DCM effect; however, its molecular mechanisms have not yet been fully elucidated. The present study indicated that BBR markedly alleviated DCM by inhibiting IL‑1β secretion and the expression of gasdermin D (Gsdmd) at the post‑transcriptional level. Considering the importance of microRNAs (miRNAs/miRs) in the regulation of the post‑transcriptional process of specific genes, the ability of BBR to upregulate the expression levels of miR‑18a‑3p by activating its promoter (‑1,000/‑500) was examined. Notably, miR‑18a‑3p targeted Gsdmd and abated pyroptosis in high glucose‑treated H9C2 cells. Moreover, miR‑18a‑3p overexpression inhibited Gsdmd expression and improved biomarkers of cardiac function in a rat model of DCM. On the whole, the findings of the present study indicate that BBR alleviates DCM by inhibiting miR‑18a‑3p‑mediated Gsdmd activation; thus, BBR may be considered a potential therapeutic agent for the treatment of DCM.
Lin Yang, Chun-Feng Cheng, Zhi-Fang Li, Xiao-Jing Huang, Shao-Qing Cai, Shan-Yu Ye, Li-Jun Zhao, Yi Xiong, Dong-Feng Chen, He-Lu Liu, Zhen-Xing Ren, Hong-Cheng Fang. Berberine blocks inflammasome activation and alleviates diabetic cardiomyopathy via the miR‑18a‑3p/Gsdmd pathway. International journal of molecular medicine. 2023 Jun;51(6)
PMID: 37114562
View Full Text