Myocardial remodeling after large infarcts in rat converts post rest-potentiation in force decay

Arq Bras Cardiol. 2012 Mar;98(3):243-51. doi: 10.1590/s0066-782x2012005000016. Epub 2012 Feb 16.
[Article in English, Portuguese, Spanish]

Abstract

Background: Post-rest contraction (PRC) of cardiac muscle provides indirect information about the intracellular calcium handling.

Objective: Our aim was to study the behavior of PRC, and its underlying mechanisms, in rats with myocardial infarction.

Methods: Six weeks after coronary occlusion, the contractility of papillary muscles (PM) obtained from sham-operated (C, n=17), moderate infarcted (MMI, n=10) and large infarcted (LMI, n=14) rats was evaluated, following rest intervals of 10 to 60 seconds before and after incubation with lithium chloride (Li(+)) substituting sodium chloride or ryanodine (Ry). Protein expression of SR Ca(2+)-ATPase (SERCA2), Na(+)/Ca(2+) exchanger (NCX), phospholamban (PLB) and phospho-Ser(16)-PLB were analyzed by Western blotting.

Results: MMI exhibited reduced PRC potentiation when compared to C. Opposing the normal potentiation for C, post-rest decays of force were observed in LMI muscles. In addition, Ry blocked PRC decay or potentiation observed in LMI and C; Li(+) inhibited NCX and converted PRC decay to potentiation in LMI. Although MMI and LMI presented decreased SERCA2 (72±7% and 47±9% of Control, respectively) and phospho-Ser(16)-PLB (75±5% and 46±11%, respectively) protein expression, overexpression of NCX (175±20%) was only observed in LMI muscles.

Conclusion: Our results showed, for the first time ever, that myocardial remodeling after MI in rats may change the regular potentiation to post-rest decay by affecting myocyte Ca(2+) handling proteins.

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Calcium-Binding Proteins / metabolism*
  • Disease Models, Animal
  • Lithium Chloride / pharmacology
  • Myocardial Contraction / drug effects*
  • Myocardial Contraction / physiology
  • Myocardial Infarction / classification
  • Myocardial Infarction / metabolism*
  • Myocytes, Cardiac / metabolism
  • Papillary Muscles / metabolism
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Ryanodine / pharmacology
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases / metabolism*
  • Sodium-Calcium Exchanger / metabolism*
  • Ventricular Remodeling / physiology*

Substances

  • Atp2a2 protein, rat
  • Calcium-Binding Proteins
  • Sodium-Calcium Exchanger
  • phospholamban
  • Ryanodine
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases
  • Lithium Chloride
  • Calcium