The Effect of Calcineurin Inhibitors on MMPs Activity in Heart and Their Side Effects-A Review of Literature

Int J Mol Sci. 2023 Jun 18;24(12):10291. doi: 10.3390/ijms241210291.

Abstract

This review focuses on the role of metalloproteinases in the pathogenesis of myocardial injury in various disease entities. It reveals how the expression and serum levels of metalloproteinases and their inhibitors change in many disease states. At the same time, the study offers a review of the impact of immunosuppressive treatment on this relationship. Modern immunosuppressive treatment is based mainly on the use of calcineurin inhibitors, including cyclosporine A and tacrolimus. The use of these drugs may carry a number of side effects, specifically to the cardiovascular system. The scale and degree of long-term influence on the organism remains unclear, but a significant risk of complications for transplant recipients who take immunosuppressive drugs as part of their daily treatment is to be expected. Therefore, the knowledge on this subject should be expanded and the negative effects of post-transplant therapy minimized. Immunosuppressive therapy plays an important role in the expression and activation of tissue metalloproteinases and their specific inhibitors, which leads to many tissue changes. The presented study is a collection of research results on the effects of calcineurin inhibitors on the heart, with particular emphasis placed on the participation of MMP-2 and MMP-9. It is also an analysis of the effects of specific heart diseases on myocardial remodeling through inductive or inhibitory effects on matrix metalloproteinases and their inhibitors.

Keywords: calcineurin inhibitors; cyclosporine A; metalloproteinases; tacrolimus.

Publication types

  • Review

MeSH terms

  • Calcineurin
  • Calcineurin Inhibitors* / adverse effects
  • Cyclosporine / adverse effects
  • Immunosuppressive Agents* / adverse effects
  • Matrix Metalloproteinases
  • Tacrolimus / adverse effects

Substances

  • Calcineurin Inhibitors
  • Immunosuppressive Agents
  • Cyclosporine
  • Tacrolimus
  • Matrix Metalloproteinases
  • Calcineurin

Grants and funding

This research received no external funding.