Beneficial effects of Mammalian target of rapamycin inhibition on left ventricular remodeling after myocardial infarction

J Am Coll Cardiol. 2009 Dec 15;54(25):2435-46. doi: 10.1016/j.jacc.2009.08.031.

Abstract

Objectives: The extent of adverse myocardial remodeling contributes essentially to the prognosis after myocardial infarction (MI). In this study we investigated whether inhibition of "mammalian target of rapamycin" (mTOR) attenuates left ventricular (LV) remodeling after MI.

Background: Therapeutic strategies to inhibit remodeling are currently limited to inhibition of neurohumoral activation. The mTOR-dependent signaling mechanisms are centrally involved in remodeling processes and provide new therapeutic opportunities.

Methods: Everolimus (RAD) treatment was initiated on the day after or 3 days after induction of myocardial infarction (MI) in rats.

Results: After 28 days, RAD-treated animals had reduced post-MI remodeling, with improved LV function and smaller LV end-diastolic diameters (8.9 + or - 0.3 mm vs. 11.4 + or - 0.2 mm, p < 0.05), end-diastolic volumes (304 + or - 30 microl vs. 414 + or - 16 microl, p < 0.05), and cardiac myocyte size (-40% vs. vehicle, p < 0.05). Infarct size was significantly reduced compared with vehicle-treated animals. The mTOR inhibition increased autophagy and concomitantly decreased proteasome activity in the border zone of the infarcted myocardium. Measurement of autophagic flux demonstrated that RAD did not decrease autophagosome clearance. When RAD treatment was initiated 3 days after MI, adverse remodeling was still attenuated and increased autophagy was still present. Sustained improvement of LV function was observed 3 months after MI, even when RAD treatment was discontinued after 1 month.

Conclusions: Inhibition of mTOR is a potential therapeutic strategy to limit infarct size and to attenuate adverse LV remodeling after MI.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atrial Natriuretic Factor / metabolism
  • Autophagy / drug effects
  • Diastole / physiology
  • Echocardiography
  • Everolimus
  • Heart Ventricles / diagnostic imaging
  • Immunosuppressive Agents / pharmacology*
  • Intracellular Signaling Peptides and Proteins / antagonists & inhibitors*
  • Intracellular Signaling Peptides and Proteins / physiology
  • Male
  • Microtubule-Associated Proteins / physiology
  • Myocardial Infarction / physiopathology*
  • Myocytes, Cardiac / pathology
  • NF-kappa B / drug effects
  • Phosphorylation
  • Protein Serine-Threonine Kinases / antagonists & inhibitors*
  • Protein Serine-Threonine Kinases / physiology
  • Rats
  • Rats, Wistar
  • Ribosomal Protein S6 Kinases, 70-kDa / drug effects
  • Sirolimus / analogs & derivatives*
  • Sirolimus / pharmacology
  • TOR Serine-Threonine Kinases
  • Up-Regulation
  • Ventricular Dysfunction, Left / physiopathology
  • Ventricular Remodeling / drug effects*
  • Ventricular Remodeling / physiology

Substances

  • Immunosuppressive Agents
  • Intracellular Signaling Peptides and Proteins
  • LC3 protein, rat
  • Microtubule-Associated Proteins
  • NF-kappa B
  • Atrial Natriuretic Factor
  • Everolimus
  • mTOR protein, rat
  • Protein Serine-Threonine Kinases
  • Ribosomal Protein S6 Kinases, 70-kDa
  • TOR Serine-Threonine Kinases
  • Sirolimus