M. Dawes et Jm. Ritter, Mg2+-induced vasodilation in human forearm vasculature is inhibited by N-G-monomethyl-L-arginine but not by indometacin, J VASC RES, 37(4), 2000, pp. 276-281
Citations number
27
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
We have investigated the mechanism of the vasodilator action of Mg2+ in hum
an forearm resistance vasculature. Venous occlusion plethysmography was use
d to measure vasodilator responses to Mg2+ infused via the brachial artery
in healthy men, and to determine effects on Mg2+ responses of indometacin (
an inhibitor of cyclo-oxygenase) and of NG-monomethyl-L-arginine (L-NMMA, a
n inhibitor of the L-arginine/nitric oxide, L-arg/ NO, pathway). Magnesium
sulphate infusion (0.05, 0.1, 0.2 mmol min(-1)) increased plasma Mg2+ conce
ntration to 1.57 +/- 0.16 mmol.l(-1) in venous blood from the infused arm a
t the highest dose. There was a dose-related increase in forearm blood flow
in the infused arm to a maximum of 6.37 +/- 1.37 ml.min(-1).dl forearm(-1)
at the highest dose corresponding to an increase of 159 +/- 25% in blood f
low relative to the non-infused arm. There was no tachyphylaxis during a se
cond infusion following a 21-min recovery period. Indometacin had no effect
on vasodilator responses to Mg2+, whereas L-NMMA inhibited Mg2+ responses
(area under the dose-response curve) by 43 +/- 6% (p = 0.0003 by repeated-m
easures ANOVA). Therefore the L-arg/NO pathway is responsible, in part, for
the vasodilator action of Mg2+ in human forearm resistance vasculature. Co
pyright (C) 2000 S. Karger AG, Basel.