A Neural Circuit Underlying the Generation of Hot Flushes.

Cell Rep

Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA; Departments of Biochemistry and Genome Sciences, University of Washington, Seattle, WA 98195, USA. Electronic address:

Published: July 2018

AI Article Synopsis

  • Hot flushes, often experienced during menopause, result from the decline of gonadal hormones and are linked to specific neurons (Kiss1 neurons) in the hypothalamus that are sensitive to these hormone levels.
  • Researchers used genetic and viral techniques in mice to show that activating these neurons triggers a response that causes blood vessels to widen, leading to flushing and lower core body temperature.
  • The study suggests that temporary activation of Kiss1 neurons after hormone withdrawal is a key factor in causing hot flushes, functioning through the release of neurokinin B in a specific brain area.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6094949PMC
http://dx.doi.org/10.1016/j.celrep.2018.06.037DOI Listing

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