4.7 Article

Neurokinin B Administration Induces Hot Flushes in Women

Journal

SCIENTIFIC REPORTS
Volume 5, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/srep08466

Keywords

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Funding

  1. MRC
  2. BBSRC
  3. NIHR
  4. Integrative Mammalian Biology (IMB) Capacity Building Award
  5. NIHR Imperial Biomedical Research Centre Funding Scheme
  6. NIHR/Wellcome Trust McMichael Clinical Research Facility
  7. AMS/Wellcome Starter Grant
  8. Wellcome Trust Translational Medicine
  9. UK
  10. Wellcome Trust
  11. National Institutes of Health Research (NIHR) [RP-2014-05-001] Funding Source: National Institutes of Health Research (NIHR)
  12. Academy of Medical Sciences (AMS) [AMS-SGCL5-Jayasena] Funding Source: researchfish
  13. National Institute for Health Research [ACF-2010-21-015, NF-SI-0507-10337, RP-2014-05-001, NF-SI-0513-10080, ACF-2011-21-004, CL-2015-21-003, ACF-2013-21-007, CL-2009-21-004, CDF-2009-02-05, CL-2014-21-003] Funding Source: researchfish

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Neurokinin B (NKB) is a hypothalamic neuropeptide binding preferentially to the neurokinin 3 receptor. Expression of the gene encoding NKB is elevated in postmenopausal women. Furthermore, rodent studies suggest that NKB signalling may mediate menopausal hot flushes. However, the effects of NKB administration on hot flushes have not been investigated in humans. To address this, we performed a randomised, double-blinded, placebo-controlled, 2-way cross-over study. Ten healthy women were admitted to a temperature and humidity-controlled research unit. Participants received 30 minute intravenous infusions of NKB and vehicle in random order. Symptoms, heart rate, blood pressure, sweating and skin temperature were compared between NKB and vehicle in a double-blinded manner. Eight of ten participants experienced flushing during NKB infusion with none experiencing flushing during vehicle infusion (P = 0.0007). Significant elevations in heart rate (P = 0.0106 vs. pre-symptoms), and skin temperature measured using skin probe (P = 0.0258 vs. pre-symptoms) and thermal imaging (P = 0.0491 vs. pre-symptoms) characteristic of menopausal flushing were observed during hot flush episodes. Our findings provide evidence that NKB administration can cause hot flushes in women. Further studies are required to determine if pharmacological blockade of NKB signalling could inhibit hot flushes during the menopause and during treatment for sex-steroid dependent cancers.

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