Endothelin receptor B is required for the blood pressure-lowering effect of G protein-coupled estrogen receptor 1 in ovariectomized rats.

Rawan N Almutlaq, David M Pollock, Eman Y Gohar
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Abstract

Activation of G protein-coupled estrogen receptor 1 (GPER1) elicits antihypertensive actions in different animal models. The endothelin-1 signaling system plays a fundamental role in blood pressure regulation. Lack of functional endothelin receptor B (ETB) evokes hypertension and salt sensitivity. GPER1 and ETB interact to promote urinary sodium excretion in female rats. We hypothesized that activation of GPER1 protects against hypertension and salt sensitivity induced by ETB antagonism in female rats. Female Sprague-Dawley rats were implanted with radiotelemetry. Animals were then subjected to ovariectomy and simultaneously implanted with minipumps to deliver either the GPER1 agonist G1 or its corresponding vehicle. Two weeks post surgery, we initiated treatment of rats with the ETB antagonist A-192621. Animals were maintained on a normal-salt diet and then challenged with a high-salt diet for an additional 5 days. Assessment of mean arterial blood pressure revealed an increase in vehicle-treated, but not G1-treated, rats in response to ovariectomy. A-192621 increased blood pressure in normal-salt diet-fed vehicle- and G1-treated rats. G1 improved the circadian blood pressure rhythms that were disrupted in A-192621-treated ovariectomized rats. Thus, although systemic GPER1 activation did not protect ovariectomized rats from hypertension and salt sensitivity induced by ETB antagonism, it maintained circadian blood pressure rhythms. Functional ETB is required to elicit the antihypertensive actions of GPER1. Additional studies are needed to improve our understanding of the interaction between G protein-coupled receptors in regulating circadian blood pressure rhythm.NEW & NOTEWORTHY Systemic G protein-coupled estrogen receptor 1 (GPER1) activation in rats prevents the increase in blood pressure evoked by ovariectomy. Blockade of endothelin receptor B negates the blood pressure-lowering impact of GPER1 in ovariectomized rats. Endothelin receptor B plays an important role in mediating the blood pressure-lowering action of GPER1 activation in female rats.

内皮素受体 B 是 G 蛋白偶联雌激素受体 1 对卵巢切除大鼠降压作用的必要条件
在不同的动物模型中,激活 G 蛋白偶联雌激素受体 1(GPER1)可产生降压作用。内皮素-1 信号系统在血压调节中发挥着重要作用。缺乏功能性内皮素受体 B 受体(ETB)会引起高血压和盐敏感性。GPER1 和 ETB 相互作用,促进雌性大鼠的尿钠排泄。我们假设,激活 GPER1 可保护雌性大鼠免受 ETB 拮抗剂诱发的高血压和盐敏感性的影响。我们给雌性 Sprague Dawley 大鼠植入了无线电遥测装置。然后,对大鼠进行卵巢切除术,并同时植入微型泵,输送 GPER1 激动剂 G1 或相应的载体(Veh)。手术后两周,我们开始用 ETB 拮抗剂 A-192621 对大鼠进行治疗。先用正常食盐(NS)喂养大鼠,然后再用高盐(HS)喂养大鼠 5 天。平均动脉血压评估显示,Veh 处理的大鼠血压升高,而 G1 处理的大鼠血压不升高,这与卵巢切除术有关。A-192621 可增加以 NS 喂养的 Veh 和 G1 处理的大鼠的血压。G1 改善了 A-192621 处理的卵巢切除大鼠的昼夜血压节律。因此,虽然全身 GPER1 激活不能保护卵巢切除大鼠免受 ETB 拮抗剂诱发的高血压和盐敏感性的影响,但却能维持昼夜节律血压。功能性 ETB 是激发 GPER1 抗高血压作用的必要条件。我们需要进行更多的研究,以进一步了解 G 蛋白偶联受体在调节昼夜血压节律中的相互作用。
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