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AJP - Cell Physiology, Vol 273, Issue 3 C834-C842, Copyright © 1997 by American Physiological Society
ARTICLES |
N. N. Tran, A. Robert, J. Atkinson and C. Capdeville-Atkinson
Laboratoire de Pharmacologie Cardio-vasculaire, Faculte de Pharmacie, Universite Henri Poincare-Nancy 1, France.
We investigated the possibility that the inhibition of oxidative phosphorylation in vascular smooth muscle attenuates norepinephrine- or KCl-evoked vasoconstriction with no change in mobilization of intracellular calcium concentration ([Ca2+]i). Experiments were performed in perfused segments of the rat tail artery loaded with the intracellular calcium dye fura 2, in the absence and presence of dinitrophenol or sodium cyanide; inhibition of oxidative phosphorylation was evaluated from the fall in intracellular ATP levels. The metabolic inhibitors reduced vasoconstriction with no change in [Ca2+]i handling, suggesting that 1) inhibition of oxidative phosphorylation attenuates vasoconstriction via a mechanism downstream of [Ca2+]i, and 2) [Ca2+]i homeostasis (both increases and decreases in [Ca2+]i) can be maintained in the presence of inhibitors of oxidative phosphorylation.
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