Virginia R Nuckols, Leena N Shoemaker, Andrew V Kuczmarski, Katherine M Haigh, Shane J McGinty, Angelica R Del Vecchio, Allyson I Schwab, David G Edwards, Hugh S Taylor, Megan M Wenner
{"title":"短期雌二醇不能恢复绝经后妇女内皮素- b受体介导的血管舒张。","authors":"Virginia R Nuckols, Leena N Shoemaker, Andrew V Kuczmarski, Katherine M Haigh, Shane J McGinty, Angelica R Del Vecchio, Allyson I Schwab, David G Edwards, Hugh S Taylor, Megan M Wenner","doi":"10.1152/ajpheart.00815.2024","DOIUrl":null,"url":null,"abstract":"<p><p>The endothelin-B receptor (ET<sub>B</sub>R) mediates vasodilation in young women, an effect that is absent in postmenopausal women. We have previously demonstrated that ET<sub>B</sub>R-mediated vasodilation is regulated by estradiol (E<sub>2</sub>) in young women; however, the impact of E<sub>2</sub> on ET<sub>B</sub>R function in postmenopausal women remains unknown. Accordingly, the objective of this study was to test the hypothesis that E<sub>2</sub> exposure restores ET<sub>B</sub>R-mediated dilation in postmenopausal women. Ten healthy postmenopausal women (55 ± 2 yr of age, 5 ± 3 years since menopause) completed the study. E<sub>2</sub> was administered by transdermal patch for 7 days (0.1 mg/day, Vivelle-Dot patch). Vasodilation in the cutaneous microcirculation (microvascular endothelial function) was measured via local heating (42°C) using laser Doppler flowmetry combined with intradermal microdialysis perfusions of lactated Ringer's (control) and ET<sub>B</sub>R antagonist (BQ-788, 300 nM) at baseline and after E<sub>2</sub> administration. There was no effect of E<sub>2</sub> on ET<sub>B</sub>R function [hormone × site, <i>F</i>(1,9) = 0.77, <i>P</i> = 0.40]. These data demonstrate that in contrast to findings in premenopausal women, E<sub>2</sub> administration does not restore ET<sub>B</sub>R function in postmenopausal women.<b>NEW & NOTEWORTHY</b> The vascular endothelial endothelin-B receptor (ET<sub>B</sub>R) mediates vasodilation in premenopausal women, an effect modulated by estradiol. ET<sub>B</sub>R-mediated vasodilation is lost in postmenopausal women, but the effect of exogenous estradiol administration on ET<sub>B</sub>R function in postmenopausal women is not known. During estradiol administration, ET<sub>B</sub>R blockade did not affect cutaneous microvascular vasodilatory response to local heating. We demonstrate that exogenous estradiol administration does not restore ET<sub>B</sub>R-mediated vasodilation in postmenopausal women.</p>","PeriodicalId":7692,"journal":{"name":"American journal of physiology. Heart and circulatory physiology","volume":" ","pages":"H327-H332"},"PeriodicalIF":4.1000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Short-term estradiol administration does not restore endothelin-B receptor-mediated vasodilation in postmenopausal women.\",\"authors\":\"Virginia R Nuckols, Leena N Shoemaker, Andrew V Kuczmarski, Katherine M Haigh, Shane J McGinty, Angelica R Del Vecchio, Allyson I Schwab, David G Edwards, Hugh S Taylor, Megan M Wenner\",\"doi\":\"10.1152/ajpheart.00815.2024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The endothelin-B receptor (ET<sub>B</sub>R) mediates vasodilation in young women, an effect that is absent in postmenopausal women. We have previously demonstrated that ET<sub>B</sub>R-mediated vasodilation is regulated by estradiol (E<sub>2</sub>) in young women; however, the impact of E<sub>2</sub> on ET<sub>B</sub>R function in postmenopausal women remains unknown. Accordingly, the objective of this study was to test the hypothesis that E<sub>2</sub> exposure restores ET<sub>B</sub>R-mediated dilation in postmenopausal women. Ten healthy postmenopausal women (55 ± 2 yr of age, 5 ± 3 years since menopause) completed the study. E<sub>2</sub> was administered by transdermal patch for 7 days (0.1 mg/day, Vivelle-Dot patch). Vasodilation in the cutaneous microcirculation (microvascular endothelial function) was measured via local heating (42°C) using laser Doppler flowmetry combined with intradermal microdialysis perfusions of lactated Ringer's (control) and ET<sub>B</sub>R antagonist (BQ-788, 300 nM) at baseline and after E<sub>2</sub> administration. There was no effect of E<sub>2</sub> on ET<sub>B</sub>R function [hormone × site, <i>F</i>(1,9) = 0.77, <i>P</i> = 0.40]. These data demonstrate that in contrast to findings in premenopausal women, E<sub>2</sub> administration does not restore ET<sub>B</sub>R function in postmenopausal women.<b>NEW & NOTEWORTHY</b> The vascular endothelial endothelin-B receptor (ET<sub>B</sub>R) mediates vasodilation in premenopausal women, an effect modulated by estradiol. ET<sub>B</sub>R-mediated vasodilation is lost in postmenopausal women, but the effect of exogenous estradiol administration on ET<sub>B</sub>R function in postmenopausal women is not known. During estradiol administration, ET<sub>B</sub>R blockade did not affect cutaneous microvascular vasodilatory response to local heating. 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引用次数: 0
摘要
内皮素- b受体(ETBR)在年轻女性中介导血管舒张,这种作用在绝经后妇女中不存在。我们之前已经证明etbr介导的血管舒张是由雌二醇(E2)在年轻女性中调节的;然而,E2对绝经后妇女ETBR功能的影响尚不清楚。因此,本研究的目的是验证E2暴露恢复绝经后妇女etbr介导的扩张的假设。10名健康绝经后妇女(55±2岁,绝经后5±3年)完成研究。E2经皮贴剂给药7 d (0.1 mg/d, Vivelle-Dot贴剂)。在基线和E2给药后,通过局部加热(42°C),使用激光多普勒血流仪结合皮内微透析灌注乳酸林格氏(对照组)和ETBR拮抗剂(BQ-788, 300 nM),测量皮肤微循环血管舒张(微血管内皮功能)。E2对ETBR功能无影响(激素*位点,F(1,9) = 0.77, P = 0.40)。这些数据表明,与绝经前妇女的研究结果相反,E2给药不能恢复绝经后妇女的ETBR功能。
Short-term estradiol administration does not restore endothelin-B receptor-mediated vasodilation in postmenopausal women.
The endothelin-B receptor (ETBR) mediates vasodilation in young women, an effect that is absent in postmenopausal women. We have previously demonstrated that ETBR-mediated vasodilation is regulated by estradiol (E2) in young women; however, the impact of E2 on ETBR function in postmenopausal women remains unknown. Accordingly, the objective of this study was to test the hypothesis that E2 exposure restores ETBR-mediated dilation in postmenopausal women. Ten healthy postmenopausal women (55 ± 2 yr of age, 5 ± 3 years since menopause) completed the study. E2 was administered by transdermal patch for 7 days (0.1 mg/day, Vivelle-Dot patch). Vasodilation in the cutaneous microcirculation (microvascular endothelial function) was measured via local heating (42°C) using laser Doppler flowmetry combined with intradermal microdialysis perfusions of lactated Ringer's (control) and ETBR antagonist (BQ-788, 300 nM) at baseline and after E2 administration. There was no effect of E2 on ETBR function [hormone × site, F(1,9) = 0.77, P = 0.40]. These data demonstrate that in contrast to findings in premenopausal women, E2 administration does not restore ETBR function in postmenopausal women.NEW & NOTEWORTHY The vascular endothelial endothelin-B receptor (ETBR) mediates vasodilation in premenopausal women, an effect modulated by estradiol. ETBR-mediated vasodilation is lost in postmenopausal women, but the effect of exogenous estradiol administration on ETBR function in postmenopausal women is not known. During estradiol administration, ETBR blockade did not affect cutaneous microvascular vasodilatory response to local heating. We demonstrate that exogenous estradiol administration does not restore ETBR-mediated vasodilation in postmenopausal women.
期刊介绍:
The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.