Effect of nitric oxide synthase inhibitors on endothelial [Ca2+]i and microvessel permeability

P. He, B. Liu, F. E. Curry

Research output: Contribution to journalArticle

63 Scopus citations

Abstract

To investigate the mechanism whereby nitric oxide (NO) signaling pathways regulate microvessel permeability in vivo, we measured changes in microvessel hydraulic conductivity (Lp) and endothelial cytoplasmic calcium concentration ([Ca2+]i) in response to calcium ionophore, ionomycin (5 μM), and ATP (10 μM) before and after the use of NO synthase (NOS) inhibitors in single perfused frog mesenteric venular microvessels. Ionomycin induced a transient increase in endothelial [Ca2+]i and an associated increase in Lp. The NOS inhibitors Nω-nitro-L-arginine methyl ester (10 and 300 μM) and Nω-monomethyl-L-arginine (L-NMMA; 10, 50, and 100 μM) significantly attenuated the peak increase in Lp induced by ionomycin. A similar inhibitory effect was also observed with the increase in Lp mediated by ATP. In contrast, D-NMMA, a biologically inactive isomer of L-NMMA, showed no effect on ionomycin-induced increase in Lp. L-Arginine (3 mM) reversed the inhibitory effect of L-NMMA (10 μM) on Lp. However, the NOS inhibitors did not alter the magnitude and time course of the biphasic increase in endothelial [Ca2+]i induced by both ionomycin and ATP. These data suggest that 1) calcium-dependent NO release is a necessary step to increase microvessel permeability, and 2) the action of NOS inhibitors in attenuating the permeability increase in response to ionomycin and ATP occurs downstream from calcium entry and does not involve modification of the initial increase in endothelial [Ca2+]i.

Original languageEnglish (US)
JournalAmerican Journal of Physiology - Heart and Circulatory Physiology
Volume41
Issue number1
StatePublished - Jan 1997

Keywords

  • Adenosine 5′-triphosphate
  • Calcium ionophore
  • Hydraulic conductivity
  • Individually perfused microvessels

ASJC Scopus subject areas

  • Physiology

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