| First Author | Semple EA | Year | 2023 |
| Journal | Front Endocrinol (Lausanne) | Volume | 14 |
| Pages | 983670 | PubMed ID | 37033219 |
| Mgi Jnum | J:345404 | Mgi Id | MGI:7462830 |
| Doi | 10.3389/fendo.2023.983670 | Citation | Semple EA, et al. (2023) Melanocortin 4 receptor signaling in Sim1 neurons permits sexual receptivity in female mice. Front Endocrinol (Lausanne) 14:983670 |
| abstractText | INTRODUCTION: Female sexual dysfunction affects approximately 40% of women in the United States, yet few therapeutic options exist for these patients. The melanocortin system is a new treatment target for hypoactive sexual desire disorder (HSDD), but the neuronal pathways involved are unclear. METHODS: In this study, the sexual behavior of female MC4R knockout mice lacking melanocortin 4 receptors (MC4Rs) was examined. The mice were then bred to express MC4Rs exclusively on Sim1 neurons (tbMC4RSim1 mice) or on oxytocin neurons (tbMC4ROxt mice) to examine the effect on sexual responsiveness. RESULTS: MC4R knockout mice were found to approach males less and have reduced receptivity to copulation, as indicated by a low lordosis quotient. These changes were independent of body weight. Lordosis behavior was normalized in tbMC4R(Sim1) mice and improved in tbMC4R(Oxt) mice. In contrast, approach behavior was unchanged in tbMC4R(Sim1) mice but greatly increased in tbMC4R(Oxt) animals. The changes were independent of melanocortin-driven metabolic effects. DISCUSSION: These results implicate MC4R signaling in Oxt neurons in appetitive behaviors and MC4R signaling in Sim1 neurons in female sexual receptivity, while suggesting melanocortin-driven sexual function does not rely on metabolic neural circuits. |
