Douglas Gillian, Cruz M Natalia, Poston Lucilla, Gustafsson Jan-Ake, Kublickiene Karolina
Maternal and Fetal Research Unit, Division of Reproduction and Endocrinology, Kings College London, London, UK.
Am J Physiol Regul Integr Comp Physiol. 2008 Jan;294(1):R112-20. doi: 10.1152/ajpregu.00421.2007. Epub 2007 Oct 24.
The role of the estrogen receptor (ER) subtypes in the modulation of vascular function is poorly understood. The aim of this study was to characterize ex vivo the functional properties of small arteries and their response to estrogens in the mesenteric circulation of female and male ER-beta knockout mice (beta-ERKO) and their wild-type (WT) littermates. Responses to changes in intraluminal flow and pressure were obtained before and after incubation with 17beta-estradiol or ER-alpha agonist propyl-pyrazole-triol (3 h; 10 nM). Cumulative concentration-response curves to acetylcholine, norepinephrine, and passive distensibility were compared with respect to sex and genotype. The collagen and elastin content within the vascular wall and ER expression were also determined. Endothelial morphology was visualized by scanning electron microscopy. 17beta-Estradiol and propyl-pyrazole-triol-treated arteries from female beta-ERKO and WT mice showed enhanced flow-mediated dilation, but this was not evident in males. Distensibility was decreased in arteries from beta-ERKO females. Sex differences in myogenic tone were observed in 17beta-estradiol-treated arteries, but were similar between beta-ERKO and WT mice. Acetylcholine- and norepinephrine-induced responses were similar between groups and sexes. ER-alpha was similarly expressed in the endothelium and media of arteries from all groups studied, as well as ER-beta in WT animals. Endothelial morphology was similar in arteries from animals of both sexes and genotype; however, arterial elastin content was decreased, and collagen content was increased in beta-ERKO male compared with WT male and with beta-ERKO female. We suggest that ERs play a sex-specific role in estrogen-mediated flow responses and distensibility, and that deletion of ER-beta affects artery structure but only in male animals. Further studies in beta-ERKO mice with established hypertension and in alpha-ERKO mice are warranted.
雌激素受体(ER)亚型在调节血管功能中的作用尚不清楚。本研究的目的是在体外表征雌性和雄性ER-β基因敲除小鼠(β-ERKO)及其野生型(WT)同窝小鼠肠系膜循环中小动脉的功能特性及其对雌激素的反应。在用17β-雌二醇或ER-α激动剂丙基吡唑三醇孵育之前和之后(3小时;10 nM),获得对管腔内流量和压力变化的反应。比较了乙酰胆碱、去甲肾上腺素和被动扩张性的累积浓度-反应曲线在性别和基因型方面的差异。还测定了血管壁内的胶原蛋白和弹性蛋白含量以及ER表达。通过扫描电子显微镜观察内皮形态。来自雌性β-ERKO和WT小鼠的经17β-雌二醇和丙基吡唑三醇处理的动脉显示出增强的血流介导的扩张,但在雄性中不明显。β-ERKO雌性小鼠的动脉扩张性降低。在经17β-雌二醇处理的动脉中观察到肌源性张力的性别差异,但在β-ERKO和WT小鼠之间相似。乙酰胆碱和去甲肾上腺素诱导的反应在各组和各性别之间相似。在所有研究组的动脉内皮和中膜中,ER-α的表达相似,在WT动物中ER-β的表达也相似。不同性别和基因型动物的动脉内皮形态相似;然而,与WT雄性和β-ERKO雌性相比,β-ERKO雄性的动脉弹性蛋白含量降低,胶原蛋白含量增加。我们认为ER在雌激素介导的血流反应和扩张性中发挥性别特异性作用,并且ER-β的缺失影响动脉结构,但仅在雄性动物中。有必要对患有高血压的β-ERKO小鼠和α-ERKO小鼠进行进一步研究。