Contractile behaviour of skinned papillary muscle in mitral valve disease

Thorac Cardiovasc Surg. 1992 Oct;40(5):253-60. doi: 10.1055/s-2007-1022721.

Abstract

The contractile behaviour of Triton-X 100 skinned left ventricular papillary muscle from 19 patients undergoing cardiac surgery for mitral valve stenosis: n = 6, mitral valve incompetence: n = 7, or combined mitral valve disease: n = 6 was analyzed. At supramaximal activation the "vibration induced force clamping technique" was used for isometric analysis of time course and extent of isometric postvibration force recovery. Afterloaded contractions were applied for extrapolation of the maximum shortening velocity at zero load (Vmax). The Calcium sensitivity was analysed by variation of the free EGTA-buffered Calcium concentration at a passive resting force of 2 mN at 26 degrees C. In different types of mitral valve disease the characteristics of isometric force development were unaltered in terms of maximum force development, force per square mm, Calcium sensitivity and the time course of isometric contraction after force clamping. However the capability to shorten as expressed by Vmax was reduced in mitral valve incompetence (3.87 +/- 0.37 ML/s) as compared with mitral valve stenosis (5.29 +/- 0.35 ML/s) or combined mitral valve disease (4.83 +/- 0.51 ML/s). The ratio between the inverse value of Vmax and the time constant of isometric force development after force clamping was significantly different in mitral valve incompetence as compared with other types of mitral valve disease (p < 0.0001). These data argue for the presence of different resistances against shortening in various types of mitral valve disease, due to altered cross-bridge cycling characteristics or to morphological factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Calcium / pharmacology
  • Heart Valve Diseases / physiopathology
  • Humans
  • In Vitro Techniques
  • Isometric Contraction
  • Isotonic Contraction
  • Middle Aged
  • Mitral Valve / drug effects
  • Mitral Valve / physiopathology*
  • Myocardial Contraction / drug effects
  • Myocardial Contraction / physiology*
  • Papillary Muscles / drug effects
  • Papillary Muscles / physiopathology*

Substances

  • Calcium