An X-Ray diffraction study on mouse cardiac cross-bridge function in vivo: effects of adrenergic {beta}-stimulation

Biophys J. 2006 Mar 1;90(5):1723-8. doi: 10.1529/biophysj.105.074062. Epub 2005 Dec 9.

Abstract

To investigate how beta-stimulation affects the contractility of cardiac muscle, x-ray diffraction from cardiac muscle in the left ventricular free wall of a mouse heart was recorded in vivo. To our knowledge, this is the first x-ray diffraction study on a heart in a living body. After the R wave in electrocardiograms, the ratio of the intensities of the equatorial (1,0) and (1,1) reflections decreased for approximately 50 ms from a diastolic value of 2.1 to a minimum of 0.8, and then recovered. The spacing of the (1,0) lattice planes increased for approximately 90 ms from a diastolic value of 37.2 nm to a maximum of 39.1 nm, and then returned to the diastolic level, corresponding to approximately 10% stretch of sarcomere. Stimulation of beta-adrenergic receptor by dobutamine (20 microg/kg/min) accelerated both the decrease in the intensity ratio, which reached a smaller systolic value, and the increase in the lattice spacing. However, the intensity ratio and spacing at the end-diastole were unchanged. The recovery of the lattice spacing during relaxation was also accelerated. The mass transfer to the thin filaments at systole in a beta-stimulated heart was close to the peak value in twitch of frog skeletal muscle at 4 degrees C, showing that the majority of cross-bridges have been recruited with few in reserve.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / physiology*
  • Actins / ultrastructure*
  • Adrenergic beta-Agonists / administration & dosage
  • Animals
  • Dobutamine / administration & dosage*
  • Heart / drug effects
  • Heart / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Myocardial Contraction / drug effects
  • Myocardial Contraction / physiology*
  • Myosins / physiology*
  • Myosins / ultrastructure*
  • Protein Conformation / drug effects
  • X-Ray Diffraction / methods

Substances

  • Actins
  • Adrenergic beta-Agonists
  • Dobutamine
  • Myosins