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Am J Physiol Heart Circ Physiol 283: H658-H663, 2002. First published April 25, 2002; doi:10.1152/ajpheart.00073.2002
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Vol. 283, Issue 2, H658-H663, August 2002

Functional NOS 1 in the rat mesenteric arterial bed

Jennifer C. Sullivan1, Ararat D. Giulumian1, David M. Pollock1,2, Leslie C. Fuchs1,3, and Jennifer S. Pollock1,3

1 Vascular Biology Center, 2 Department of Physiology, and 3 Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta, Georgia 30912

Previously we have demonstrated functional nitric oxide synthase (NOS) 1 in large arteries. Because resistance arteries largely determine blood pressure, this study examined whether functional NOS 1 also exists in resistance arteries. Phenylephrine (PE) contraction was measured in the absence and presence of the NOS 1 inhibitor N5-(1-imino-3-butenyl)-L-ornithine (VNIO) in isolated mesenteric resistance arteries (endothelium intact and denuded) from Sprague-Dawley rats. For NOS 1 activity and expression, the mesenteric arterial bed was separated into cytosolic and particulate fractions. NOS activity was assayed by measuring the conversion of [3H]arginine to [3H]citrulline inhibited by a nonselective NOS inhibitor or VNIO. VNIO increased PE sensitivity in endothelium-intact and -denuded arteries. In cytosolic and particulate fractions of the arterial bed, ~40% of NOS activity was inhibited by VNIO. Immunoprecipitation and Western blot analysis revealed two NOS 1 immunoreactive bands. One band corresponded to the rat brain isoform, whereas the second was of a slightly lower molecular mass. The cytosolic fraction contained both isoforms; however, the particulate fraction had only the lower molecular mass form. These studies demonstrate the existence of functional NOS 1 in resistance arteries.

neuronal nitric oxide synthase activity; resistance arteries; vascular reactivity; subcellular fractionation


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