Department of Physiology, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Am J Physiol Heart Circ Physiol. 2020 Apr 1;318(4):H820-H829. doi: 10.1152/ajpheart.00734.2019. Epub 2020 Feb 21.
Estrogen deficiency is considered to be an important factor leading to cardiovascular diseases (CVDs). Indeed, the prevalence of CVDs in postmenopausal women exceeds that of premenopausal women and men of the same age. Recent research findings provide evidence that estrogen plays a pivotal role in the regulation of calcium homeostasis and therefore fine-tunes normal cardiomyocyte contraction and relaxation processes. Disruption of calcium homeostasis is closely associated with the pathological mechanism of CVDs. Thus, this paper maps out and summarizes the effects and mechanisms of estrogen on calcium handling proteins in cardiac myocytes, including L-type Ca channel, the sarcoplasmic reticulum Ca release channel named ryanodine receptor, sarco(endo)plasmic reticulum Ca-ATPase, and sodium-calcium exchanger. In so doing, we provide theoretical and experimental evidence for the successful design of estrogen-based prevention and treatment therapies for CVDs.
雌激素缺乏被认为是导致心血管疾病(CVDs)的一个重要因素。事实上,绝经后妇女 CVD 的患病率超过了同年龄的绝经前妇女和男性。最近的研究结果提供了证据,表明雌激素在钙稳态的调节中起着关键作用,从而精细地调节正常心肌细胞的收缩和松弛过程。钙稳态的破坏与 CVD 的病理机制密切相关。因此,本文概述并总结了雌激素对心肌细胞中钙处理蛋白的作用及其机制,包括 L 型钙通道、肌浆网 Ca 释放通道(即兰尼碱受体)、肌浆网/内质网 Ca-ATP 酶和钠钙交换体。这样,我们为基于雌激素的 CVD 预防和治疗策略的成功设计提供了理论和实验证据。