Effect of miR-21/TLR4/NF-κB pathway on myocardial apoptosis in rats with myocardial ischemia-reperfusion

Y-Q Pan1, J Li, X-W Li

  • 1Department of Cardiology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China. linjiafeng_wzmcfey@163.com.

Abstract

Insights

Myocardial ischemia-reperfusion injury in rats decreases microRNA-21 (miR-21) levels. Overexpressing miR-21 protects the heart by inhibiting the Toll-like receptor 4 (TLR4)/nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) pathway, reducing apoptosis and inflammation.

Area of Science:

  • Cardiovascular Biology
  • Molecular Medicine
  • Regenerative Medicine

Background:

  • Myocardial ischemia-reperfusion (I/R) injury is a major cause of heart damage.
  • The role of micro ribonucleic acid (miR)-21 in I/R injury and its downstream signaling pathways remains incompletely understood.

Purpose of the Study:

  • To investigate the influence of miR-21 and the Toll-like receptor 4 (TLR4)/nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) pathway on myocardial apoptosis.
  • To determine the therapeutic potential of miR-21 in mitigating I/R injury.

Main Methods:

  • Utilized a rat model of myocardial I/R injury.
  • Employed recombinant adeno-associated virus vectors for miR-21 overexpression.
  • Assessed cardiac function, infarct size, apoptosis (TUNEL), and protein/cytokine levels (Western blot, ELISA).

Main Results:

  • Myocardial I/R injury significantly reduced miR-21 expression and cardiac function while increasing apoptosis.
  • Overexpression of miR-21 improved cardiac function and reduced infarct size and apoptosis.
  • miR-21 overexpression suppressed the TLR4/NF-κB pathway, decreasing pro-apoptotic proteins (Caspase-3, Bax) and inflammatory cytokines (IL-6).

Conclusions:

  • Myocardial I/R injury is associated with decreased miR-21 levels.
  • Upregulating miR-21 offers a protective effect against myocardial I/R injury by inhibiting the TLR4/NF-κB pathway.
  • miR-21 represents a potential therapeutic target for treating myocardial I/R injury.

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