Key result
Endothelin increased myocyte velocity of shortening by 32.8 +/- 2.3 microns/s in control pigs, but decreased it by 8.3 +/- 2.2 microns/s in pigs with pacing-induced congestive heart failure.
Why the study?
Does exogenous endothelin have differential effects on myocyte contractility in pacing-induced heart failure compared to normal controls?
Does exogenous endothelin have differential effects on myocyte contractility in pacing-induced heart failure compared to normal controls?
Endothelin increases contractility in normal cardiac myocytes but decreases it in failing myocytes, suggesting differential pathophysiological effects in the setting of heart failure.
Endothelin may impair myocyte contractility in failing hearts; hypothesis-generating for differential effects in pacing-induced HF models.
Increased plasma concentrations of endothelin have been identified in patients and animals with severe congestive heart failure (CHF). However, whether and to what extent increased endothelin (ET) concentrations influence left ventricular (LV) myocyte contractility, ET-receptor subtype density, and endogenous ET production with the development of CHF remains unclear. Accordingly, myocyte contractile function, response to ET, sarcolemmal ET-receptor density, and myocyte ET production were examined in pigs following the development of pacing-induced CHF (240 beats/min, 3 wk, n = 8) and in controls (n = 8). With CHF, plasma ET increased over threefold. In the presence of ET (10-500 pM), myocyte contractility increased in a dose-dependent manner in control myocytes but decreased in CHF myocytes. For example, in the presence of 200 pM ET, velocity of shortening increased by 32.8 +/- 2.3 microns/s in controls but decreased by 8.3 +/- 2.2 microns/s with CHF. LV sarcolemmal ET-receptor density was primarily of the ETA-receptor subtype in controls (96 +/- 1.0%) and was unchanged with CHF. In quiescent myocyte preparations, control myocytes secreted ET (2.29 +/- 0.45 amol.cell-1.h-1), which was similar in CHF myocytes. These findings suggest that the production of ET may have important and potentially differential effects on contractile function with the development of CHF.
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Thomas et al. (1996) studied Congestive heart failure (n=16). Endothelin vs. Control myocytes was evaluated on Myocyte contractility (velocity of shortening). Endothelin increased myocyte velocity of shortening by 32.8 +/- 2.3 microns/s in control pigs, but decreased it by 8.3 +/- 2.2 microns/s in pigs with pacing-induced congestive heart failure.
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