Cerebral microvascular dilation during hypotension and decreased oxygen tension: A role for nNOS

Holly D. Bauser-Heaton, H. Glenn Bohlen

Research output: Contribution to journalArticle

41 Scopus citations

Abstract

Endothelial (eNOS) and neuronal nitric oxide synthase (nNOS) are implicated as important contributors to cerebral vascular regulation through nitric oxide (NO). However, direct in vivo measurements of NO in the brain have not been used to dissect their relative roles, particularly as related to oxygenation of brain tissue. We found that, in vivo, rat cerebral arterioles had increased NO concentration ([NO]) and diameter at reduced periarteriolar oxygen tension (PO2) when either bath oxygen tension or arterial pressure was decreased. Using these protocols with highly selective blockade of nNOS, we tested the hypothesis that brain tissue nNOS could donate NO to the arterioles at rest and during periods of reduced perivascular oxygen tension, such as during hypotension or reduced local availability of oxygen. The decline in periarteriolar PO2 by bath manipulation increased [NO] and vessel diameter comparable with responses at similarly decreased PO2 during hypotension. To determine whether the nNOS provided much of the vascular wall NO, nNOS was locally suppressed with the highly selective inhibitor N-(4S)-(4-amino-5-[aminoethyl]aminopentyl)-N′-nitroguanidine. After blockade, resting [NO], PO2, and diameters decreased, and the increase in [NO] during reduced PO2 or hypotension was completely absent. However, flow-mediated dilation during occlusion of a collateral arteriole did remain intact after nNOS blockade and the vessel wall [NO] increased to ∼80% of normal. Therefore, nNOS predominantly increased NO during decreased periarteriolar oxygen tension, such as that during hypotension, but eNOS was the dominant source of NO for flow shear mechanisms.

Original languageEnglish (US)
Pages (from-to)H2193-H2201
JournalAmerican Journal of Physiology - Heart and Circulatory Physiology
Volume293
Issue number4
DOIs
StatePublished - Oct 1 2007

Keywords

  • Arterioles
  • Brain
  • In vivo
  • Microelectrode
  • Neuronal nitric oxide synthase
  • Nitric oxide

ASJC Scopus subject areas

  • Physiology

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