Characteristics of myocytes isolated from hearts of renovascular hypertensive guinea pigs

Am J Physiol. 1994 May;266(5 Pt 2):H1886-95. doi: 10.1152/ajpheart.1994.266.5.H1886.

Abstract

A model of renovascular hypertension has been developed in the guinea pig using the Goldblatt (2-kidney, 1-clip) operation. Systolic and diastolic blood pressures were significantly increased 3 and 7 wk after the operation, but levels fell to control values at 11 wk. The two-dimensional areas of myocytes isolated from the hearts of Goldblatt-operated (GB) animals were larger than those in control cells at 3 wk (cf. 3,397 +/- 87 and 2,208 +/- 125 microns 2, P < 0.01), and the difference was maintained at 7 and 11 wk. No change in cell contraction or relaxation characteristics were seen at either 3 or 7 wk after clipping. Myocytes from the 11-wk GB group showed a significantly reduced contraction amplitude and velocity at 32 degrees C in maximally activating Ca2+ or isoproterenol concentrations (%cell shortening in Ca2+, cf. 6.8 +/- 0.4 and 10.0 +/- 0.9, P < 0.01). Concentrations eliciting 50% of maximal response for Ca2+ or isoproterenol were unchanged, as was the ratio of isoproterenol to Ca2+ effect in the same cell. Increases in time to peak contraction (TTP) and time to 50% relaxation (R50) were observed in 11-wk GB myocytes, but only at room temperature. There was no lengthening of TTP or R50 of the Ca2+ transient, nor was there any change in Ca2+ current density or inactivation kinetics in these myocytes.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Pressure
  • Body Weight
  • Calcium / metabolism*
  • Calcium / pharmacology
  • Cell Nucleus / pathology
  • Cell Nucleus / ultrastructure
  • Cells, Cultured
  • Electric Stimulation
  • Guinea Pigs
  • Heart / drug effects
  • Heart / physiopathology*
  • Hypertension, Renovascular / physiopathology*
  • Indoles
  • Isoproterenol / pharmacology
  • Male
  • Membrane Potentials
  • Microscopy, Fluorescence
  • Myocardial Contraction* / drug effects
  • Myocardium / metabolism
  • Myocardium / pathology
  • Organ Size
  • Time Factors

Substances

  • Indoles
  • Indo-1 pentaacetoxymethyl ester
  • Isoproterenol
  • Calcium