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Updated: Jan 20, 2026

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Effect of miR-9 on myocardial fibrosis in rats via TGF-β1/Smads signaling pathway

X Jin1, L-L Yu, C-X Yu

  • 1Department of Cardiology, Yantai Hospital of Traditional Chinese Medicine, Yantai, China. yucx05@163.com.

Abstract

Insights

MicroRNA-9 (miR-9) alleviates myocardial fibrosis in rats by inhibiting the TGF-β1/Smads pathway. This study observed miR-9's effect on cardiac fibrosis and its underlying mechanism.

Area of Science:

  • Cardiovascular Biology
  • Molecular Medicine
  • Fibrosis Research

Background:

  • Myocardial fibrosis (MF) is a significant pathological process.
  • Understanding the molecular mechanisms regulating MF is crucial for developing therapeutic strategies.

Purpose of the Study:

  • To investigate the therapeutic effect of microRNA-9 (miR-9) on myocardial fibrosis in a rat model.
  • To elucidate the underlying molecular mechanism of miR-9 in regulating myocardial fibrosis.

Main Methods:

  • Myocardial fibrosis was induced in rats.
  • Rats were divided into Sham, Model, and miR-9 treatment groups.
  • Key indicators measured included heart/body weight ratios, hydroxyproline content, collagen levels (Type I and III), miR-9 expression, and TGF-β1/Smads2 protein levels via RT-PCR and Western blotting.

Main Results:

  • Rats with induced myocardial fibrosis showed increased heart/body weight ratios, hydroxyproline, collagen I and III, TGF-β1, and Smads2 levels, alongside decreased miR-9 expression compared to controls.
  • miR-9 treatment significantly reversed these pathological changes, reducing fibrosis markers and TGF-β1/Smads2 signaling.

Conclusions:

  • MicroRNA-9 (miR-9) demonstrates a protective effect against myocardial fibrosis in rats.
  • The mechanism involves the inhibition of the transforming growth factor-β1 (TGF-β1)/Smads signaling pathway.

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