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ABSTRACT: Objective
Genetically diverse UM-HET3 (HET3) mice have emerged as a more robust model of human large artery dysfunction than the commonly used inbred C57BL/6J (C57) mice. However, HET3 resistance artery function has not been examined. The purpose of this study was to examine HET3 versus C57 mesenteric resistance artery agonist-induced vasomotor responses to phenylephrine (PE) and acetylcholine (ACh), PE-induced myoendothelial feedback (endothelium-dependent feedback dilation to PE-induced vasoconstriction) and its underlying mechanisms, and eNOS (an enzyme involved in endothelium-dependent dilation) expression.Hypothesis
Vasomotor responses, mechanisms, and eNOS protein expression would be similar between HET3 and C57 mesenteric resistance arteries of both sexes.Methods
SUBMITTER: Looft-Wilson RC
PROVIDER: S-EPMC12702883 | biostudies-literature | 2025
REPOSITORIES: biostudies-literature