Literature DB >> 14764441

Direct effect of ethanol on human vascular function.

Ahmed Tawakol1, Torbjørn Omland, Mark A Creager.   

Abstract

Epidemiological studies indicate that moderate ethanol consumption reduces cardiovascular mortality. Cellular and animal data suggest that ethanol confers beneficial effects on the vascular endothelium and increases the bioavailability of nitric oxide. The purpose of this study was to assess the effect of ethanol on endothelium-dependent, nitric oxide-mediated vasodilation in healthy human subjects. Forearm blood flow (FBF) was determined by venous occlusion plethysmography in healthy human subjects during intra-arterial infusions of either methacholine (0.3, 1.0, 3.0, and 10.0 mcg/min, n = 9), nitroprusside (0.3, 1.0, 3.0, and 10.0 mcg/min, n = 9), or verapamil (10, 30, 100, and 300 mcg/min, n = 8) before and during the concomitant intra-arterial infusions of ethanol (10% ethanol in 5% dextrose). Additionally, a time control experiment was conducted, during which the methacholine dose-response curve was measured twice during vehicle infusions (n = 5). During ethanol infusion, mean forearm and systemic alcohol levels were 227 +/- 30 and 6 +/- 0 mg/dl, respectively. Ethanol infusion alone reduced FBF (2.5 +/- 0.1 to 1.9 +/- 0.1 ml.dl(-1).min(-1), P < 0.05). Despite initial vasoconstriction, ethanol augmented the FBF dose-response curves to methacholine, nitroprusside, and verapamil (P < 0.01 by ANOVA for each). To determine whether this augmented FBF response was related to shear-stress-induced release of nitric oxide, FBF was measured during the coinfusion of ethanol and N(G)-nitro-L-arginine (L-NAME; n = 8) at rest and during verapamil-induced vasodilation. The addition of L-NAME did not block the ability of ethanol to augment verapamil-induced vasodilation. Ethanol has complex direct vascular effects, which include basal vasoconstriction as well as potentiation of both endothelium-dependent and -independent vasodilation. None of these effects appear to be mediated by an increase in nitric oxide bioavailability, thus disputing findings from preclinical models.

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Year:  2004        PMID: 14764441     DOI: 10.1152/ajpheart.01207.2003

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


  6 in total

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2.  Chronic ethanol ingestion increases aortic endothelial nitric oxide synthase expression and nitric oxide production in the rat.

Authors:  Dean J Kleinhenz; Roy L Sutliff; John A Polikandriotis; Erik R Walp; Sergey I Dikalov; David M Guidot; C Michael Hart
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3.  Ethanol exposure alters early cardiac function in the looping heart: a mechanism for congenital heart defects?

Authors:  Ganga Karunamuni; Shi Gu; Yong Qiu Doughman; Lindsy M Peterson; Katherine Mai; Quinn McHale; Michael W Jenkins; Kersti K Linask; Andrew M Rollins; Michiko Watanabe
Journal:  Am J Physiol Heart Circ Physiol       Date:  2013-11-22       Impact factor: 4.733

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Review 5.  Current Knowledge on the Vascular Effects of Menthol.

Authors:  Henrique Silva
Journal:  Front Physiol       Date:  2020-04-07       Impact factor: 4.566

6.  The effects of alcohol consumption on flow-mediated dilation in humans: A systematic review.

Authors:  Chueh-Lung Hwang; Mariann R Piano; Shane A Phillips
Journal:  Physiol Rep       Date:  2021-05
  6 in total

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