4.8 Article

Melanocortin 4 receptor agonism enhances sexual brain processing in women with hypoactive sexual desire disorder

Journal

JOURNAL OF CLINICAL INVESTIGATION
Volume 132, Issue 19, Pages -

Publisher

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI152341

Keywords

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Funding

  1. AMAG Pharmaceuticals Inc.
  2. Medical Research Council (MRC) [MR/T006242/1]
  3. National Institute for Health Research (NIHR) [CS-2018-18-ST2-002, RP-2014-05-001]
  4. National Institutes of Health Research (NIHR) [CS-2018-18-ST2-002] Funding Source: National Institutes of Health Research (NIHR)

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The study involved 31 premenopausal heterosexual women with HSDD in a double-blinded crossover trial, and found that MC4R agonism significantly increased sexual desire and enhanced sexual brain processing, including reducing self-consciousness and increasing sensitivity to erotic stimuli.
BACKGROUND. Hypoactive sexual desire disorder (HSDD) is characterized by a persistent deficiency of sexual fantasies and desire for sexual activity, causing marked distress and interpersonal difficulty. It is the most prevalent female sexual health problem globally, affecting approximately 10% of women, but has limited treatment options. Melanocortin 4 receptor (MC4R) agonists have emerged as a promising therapy for women with HSDD, through unknown mechanisms. Studying the pathways involved is crucial for our understanding of normal and abnormal sexual behavior. METHODS. Using psychometric, functional neuroimaging, and hormonal analyses, we conducted a randomized, double -blinded, placebo-controlled, crossover clinical study to assess the effects of MC4R agonism compared with placebo on sexual brain processing in 31 premenopausal heterosexual women with HSDD.RESULTS. MC4R agonism significantly increased sexual desire for up to 24 hours after administration compared with placebo. During functional neuroimaging, MC4R agonism enhanced cerebellar and supplementary motor area activity and deactivated the secondary somatosensory cortex, specifically in response to visual erotic stimuli, compared with placebo. In addition, MC4R agonism enhanced functional connectivity between the amygdala and the insula during visual erotic stimuli compared with placebo. CONCLUSION. These data suggest that MC4R agonism enhanced sexual brain processing by reducing self-consciousness, increasing sexual imagery, and sensitizing women with HSDD to erotic stimuli. These findings provide mechanistic insight into the action of MC4R agonism in sexual behavior and are relevant to the ongoing development of HSDD therapies and MC4R agonist development more widely.

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