Inhibition of mTOR signaling with rapamycin regresses established cardiac hypertrophy induced by pressure overload

Circulation. 2004 Jun 22;109(24):3050-5. doi: 10.1161/01.CIR.0000130641.08705.45. Epub 2004 Jun 7.

Abstract

Background: Rapamycin is a specific inhibitor of the mammalian target of rapamycin (mTOR). We recently reported that administration of rapamycin before exposure to ascending aortic constriction significantly attenuated the load-induced increase in heart weight by approximately 70%.

Methods and results: To examine whether rapamycin can regress established cardiac hypertrophy, mice were subjected to pressure overload (ascending aortic constriction) for 1 week, echocardiography was performed to verify an increase in ventricular wall thickness, and mice were given rapamycin (2 mg x kg(-1) x d(-1)) for 1 week. After 1 week of pressure overload (before treatment), 2 distinct groups of animals became apparent: (1) mice with compensated cardiac hypertrophy (normal function) and (2) mice with decompensated hypertrophy (dilated with depressed function). Rapamycin regressed the pressure overload-induced increase in heart weight/body weight (HW/BW) ratio by 68% in mice with compensated hypertrophy and 41% in mice with decompensated hypertrophy. Rapamycin improved left ventricular end-systolic dimensions, fractional shortening, and ejection fraction in mice with decompensated cardiac hypertrophy. Rapamycin also altered the expression of some fetal genes, reversing, in part, changes in alpha-myosin heavy chain and sarcoplasmic reticulum Ca2+ ATPase.

Conclusions: Rapamycin may be a therapeutic tool to regress established cardiac hypertrophy and improve cardiac function.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adaptation, Physiological
  • Animals
  • Aorta
  • Aortic Diseases / complications
  • Cardiomegaly / drug therapy*
  • Cardiomegaly / etiology
  • Cell Size / drug effects
  • Constriction, Pathologic / complications
  • Drug Evaluation, Preclinical
  • Gene Expression Regulation / drug effects
  • Male
  • Mice
  • Myocytes, Cardiac / pathology
  • Organ Size / drug effects
  • Phosphorylation
  • Protein Kinases / drug effects*
  • Protein Kinases / physiology
  • Protein Processing, Post-Translational / drug effects
  • Ribosomal Protein S6 / metabolism
  • Sirolimus / pharmacology
  • Sirolimus / therapeutic use*
  • Stroke Volume / drug effects
  • TOR Serine-Threonine Kinases

Substances

  • Ribosomal Protein S6
  • Protein Kinases
  • mTOR protein, mouse
  • TOR Serine-Threonine Kinases
  • Sirolimus