Hay Meredith, Xue Baojian, Johnson Alan Kim
Department of Physiology, University of Arizona, 1501 N Campbell Rd Bldg 201, Rm 4103, Tucson, AZ, 85724, USA,
Curr Hypertens Rep. 2014 Aug;16(8):458. doi: 10.1007/s11906-014-0458-4.
The role of the brain in hypertension between the sexes is known to be important especially with regards to the effects of circulating sex hormones. A number of different brain regions important for regulation of sympathetic outflow and blood pressure express estrogen receptors (ERα and ERβ). Estradiol, acting predominantly via the ERα, inhibits angiotensin II activation of the area postrema and subfornical organ neurons and inhibits reactive oxygen generation that is required for the development of Angiotensin II-induced neurogenic hypertension. Estradiol activation of ERβ within the paraventricular nucleus and the rostral ventral lateral medulla inhibits these neurons and inhibits angiotensin II, or aldosterone induced increases in sympathetic outflow and hypertension. Understanding the cellular and molecular mechanisms underlying ERα and ERβ actions within key brain regions regulating blood pressure will be essential for the development of "next generation" selective estrogen receptor modulators (SERMS) that can be used clinically for the treatment of neurogenic hypertension.
众所周知,大脑在两性高血压中所起的作用非常重要,尤其是在循环性激素的影响方面。许多对交感神经输出和血压调节至关重要的不同脑区都表达雌激素受体(ERα和ERβ)。雌二醇主要通过ERα发挥作用,抑制最后区和穹窿下器官神经元的血管紧张素II激活,并抑制血管紧张素II诱导的神经源性高血压发展所需的活性氧生成。雌二醇激活室旁核和延髓头端腹外侧的ERβ可抑制这些神经元,并抑制血管紧张素II或醛固酮诱导的交感神经输出增加和高血压。了解调节血压的关键脑区内ERα和ERβ作用的细胞和分子机制,对于开发可临床用于治疗神经源性高血压的“下一代”选择性雌激素受体调节剂(SERMs)至关重要。