Freedman R R, Woodward S, Sabharwal S C
Lafayette Clinic, Detroit, Michigan.
Obstet Gynecol. 1990 Oct;76(4):573-8.
It has been hypothesized that hot flushes are triggered within the hypothalamus by alpha 2-adrenergic receptors on noradrenergic neurons. We administered intravenous clonidine (an alpha 2-adrenergic agonist) and yohimbine (an alpha 2-adrenergic antagonist) to nine menopausal women with hot flushes and to an asymptomatic comparison group. Hot flushes were defined objectively by skin conductance responses recorded from the sternum; finger temperature recordings and symptom reports were also evaluated. The subjects were prescreened using ambulatory skin conductance monitoring. A significantly greater number of hot flushes occurred during yohimbine sessions than in corresponding placebo sessions (six versus zero). Clonidine significantly increased the amount of peripheral heating needed to provoke a hot flush (40.6 versus 33.6 minutes) and reduced the number of hot flushes that did occur (two versus eight). No hot flushes occurred in the asymptomatic women. These findings support the role of a central alpha 2-adrenergic mechanism in the initiation of hot flushes.
有假说认为,潮热是由去甲肾上腺素能神经元上的α2 - 肾上腺素能受体在下丘脑内触发的。我们对9名有潮热症状的绝经后女性和一个无症状的对照组静脉注射可乐定(一种α2 - 肾上腺素能激动剂)和育亨宾(一种α2 - 肾上腺素能拮抗剂)。通过记录胸骨处的皮肤电导反应客观地定义潮热;还评估了手指温度记录和症状报告。使用动态皮肤电导监测对受试者进行预筛选。与相应的安慰剂疗程相比,育亨宾疗程期间出现的潮热数量显著更多(6次对0次)。可乐定显著增加诱发潮热所需的外周加热量(40.6分钟对33.6分钟),并减少实际出现的潮热次数(2次对8次)。无症状女性未出现潮热。这些发现支持中枢α2 - 肾上腺素能机制在潮热发作中的作用。