Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA.
Graduate Program in Neuroscience, University of Washington, Seattle, WA 98195, USA; Departments of Biochemistry and Genome Sciences, University of Washington, Seattle, WA 98195, USA.
Cell Rep. 2018 Jul 10;24(2):271-277. doi: 10.1016/j.celrep.2018.06.037.
Hot flushes are a sudden feeling of warmth commonly associated with the decline of gonadal hormones at menopause. Neurons in the arcuate nucleus of the hypothalamus that express kisspeptin and neurokinin B (Kiss1 neurons) are candidates for mediating hot flushes because they are negatively regulated by sex hormones. We used a combination of genetic and viral technologies in mice to demonstrate that artificial activation of Kiss1 neurons evokes a heat-dissipation response resulting in vasodilation (flushing) and a corresponding reduction of core-body temperature in both females and males. This response is sensitized by ovariectomy. Brief activation of Kiss1 axon terminals in the preoptic area of the hypothalamus recapitulates this response, while pharmacological blockade of neurokinin B (NkB) receptors in the same brain region abolishes it. We conclude that transient activation of Kiss1 neurons following sex-hormone withdrawal contributes to the occurrence of hot flushes via NkB release in the rostral preoptic area.
热潮是一种突然的温暖感,通常与绝经时性腺激素下降有关。下丘脑弓状核中表达 kisspeptin 和神经激肽 B(Kiss1 神经元)的神经元是介导热潮的候选者,因为它们受性激素的负调控。我们使用小鼠中的遗传和病毒技术组合证明,人工激活 Kiss1 神经元会引发散热反应,导致血管舒张(脸红)和雌性和雄性的核心体温相应降低。这种反应会因卵巢切除术而敏感化。短暂激活下丘脑视前区的 Kiss1 轴突末梢会重现这种反应,而在同一脑区阻断神经激肽 B(NkB)受体则会消除这种反应。我们得出结论,性荷尔蒙撤退后 Kiss1 神经元的短暂激活通过在视前区释放 NkB 导致热潮的发生。