Literature DB >> 12124213

Functional NOS 1 in the rat mesenteric arterial bed.

Jennifer C Sullivan1, Ararat D Giulumian, David M Pollock, Leslie C Fuchs, Jennifer S Pollock.   

Abstract

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 N(5)-(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 [(3)H]arginine to [(3)H]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, approximately 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.

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Year:  2002        PMID: 12124213     DOI: 10.1152/ajpheart.00073.2002

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   4.733


  7 in total

1.  Renal NOS activity, expression, and localization in male and female spontaneously hypertensive rats.

Authors:  Jennifer C Sullivan; Jennifer L Pardieck; Kelly A Hyndman; Jennifer S Pollock
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2009-11-04       Impact factor: 3.619

2.  Nitric oxide produced by endothelial nitric oxide synthase promotes diuresis.

Authors:  Jazmin M Perez-Rojas; Kamal M Kassem; William H Beierwaltes; Jeffrey L Garvin; Marcela Herrera
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2010-02-10       Impact factor: 3.619

3.  IL-10 treatment decreases blood pressure in male, but not female, spontaneously hypertensive rats.

Authors:  Ellen E Gillis; Jacqueline B Musall; Babak Baban; Jennifer C Sullivan
Journal:  Am J Physiol Renal Physiol       Date:  2020-07-20

4.  Nitric oxide synthase-mediated blood pressure regulation in obese melanocortin-4 receptor-deficient pregnant rats.

Authors:  Frank T Spradley; Jennifer M Sasser; Jacqueline B Musall; Jennifer C Sullivan; Joey P Granger
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2016-08-17       Impact factor: 3.619

5.  Distinct regulation of inner medullary collecting duct nitric oxide production from mice and rats.

Authors:  Kelly A Hyndman; Jing Xue; Alexander MacDonell; Joshua S Speed; Chunhua Jin; Jennifer S Pollock
Journal:  Clin Exp Pharmacol Physiol       Date:  2013-03       Impact factor: 2.557

6.  Female sex hormones protect against salt-sensitive hypertension but not essential hypertension.

Authors:  Krystal N Brinson; Olga Rafikova; Jennifer C Sullivan
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2014-07-15       Impact factor: 3.619

7.  Lack of contribution of nitric oxide synthase to cholinergic vasodilation in murine renal afferent arterioles.

Authors:  Sungmi Park; Benjamin J Bivona; Lisa M Harrison-Bernard
Journal:  Am J Physiol Renal Physiol       Date:  2018-02-07
  7 in total

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