Male ejaculation acutely suppresses sexual motivation in male mice. In contrast, relatively little is known about how male ejaculation affects sexual motivation and sexual behavior in female mice. How the brain responds to the completion of mating is also unclear. Here, by using a self-paced mating assay, we first demonstrate that female mice show decreased sexual motivation acutely after experiencing male ejaculation. By using brain-wide analysis of activity-dependent labeling, we next pin-pointed the medial preoptic area as a brain region strongly activated during the post-ejaculatory period. Furthermore, using freely moving calcium imaging to compare the neural activity of inhibitory and excitatory neurons in the medial preoptic area, we revealed that a subset of the neurons in this region responds significantly and specifically to male ejaculation but not to female-to-male sniffing or to male mounting. While there were excitatory and inhibitory neurons that showed increased response to male ejaculation, the response magnitude as well as the proportion of neurons responding to the event was significantly larger in the inhibitory neuron population. Next, by unbiased classification of their responses, we also found a subpopulation of neurons that increase their activity late after the onset of male ejaculation. These neurons were all inhibitory indicating that male ejaculation induces a prolonged inhibitory activity in the medial preoptic area. Lastly, we found that chemogenetic activation of medial preoptic area neurons that were active during the post-ejaculatory period, but not during appetitive or consummatory periods, were sufficient to suppress female sexual motivation. Together, our data illuminate the importance of the medial preoptic area as a brain node which encodes a negative signal that sustains a low sexual motivation state after the female mice experience ejaculation.
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http://dx.doi.org/10.7554/eLife.91765 | DOI Listing |
Reprod Domest Anim
March 2025
College of Veterinary Science & A.H., NDVSU, Jabalpur, Madhya Pradesh, India.
The oxidative status of seminal fluid is a critical factor in producing high-quality sperm doses for artificial insemination. This study aimed to investigate the impact of seasonal variations on oxidative stress biomarkers and ROMO1 (Reactive Oxygen Modulator 1) gene expression in Barbari and Sirohi bucks. Four ejaculates of adult breeding Barbari and Sirohi bucks, six from each breed, were collected fortnightly using an artificial vagina during the summer and winter seasons for the study.
View Article and Find Full Text PDFSci Rep
March 2025
Department of Urology, University Medical Center Utrecht, Utrecht, The Netherlands.
The male urethra transports urine and semen. Any disease of the male urethra, hindering normal voiding or ejaculation, has a major impact on quality of life. Urethral stricture disease is common and molecular research into urethral strictures is hampered by the lack of reliable models of the human urethra.
View Article and Find Full Text PDFPLoS One
March 2025
Discipline of Pharmaceutical Sciences, School of Health Sciences, Westville Campus, University of KwaZulu-Natal, Durban, South Africa.
Introduction: There is an ongoing global upsurge of opioid misuse, fatal overdose and other related disorders, significantly affecting the African continent, due to resource-limited settings and poor epidemiological surveillance systems. This scoping review maps scientific evidence on epidemiological data on unlawful opioid use to identify knowledge gaps and policy shortcomings.
Method: The databases (PubMed, Scopus, Web of Sciences) and references were searched guided by Population, Concept, and Context (PCC) and PRISMA-ScR.
Reprod Domest Anim
March 2025
Laboratory of Animal Germplasm Conservation, Department of Animal Sciences, Federal University of the Semiarid Region-UFERSA, Mossoró, Brazil.
The advancement of short-term storage methods for collared peccary semen targets its potential application in artificial insemination programmes and for combination with cryopreservation techniques. The objective of this study was to evaluate the performance of a transport container (Botutainer) for the preservation of collared peccary semen using commercial extenders (BTS, NUTRIXcell+ and PRIMXcell Ultra) as well as a TRIS + egg yolk extender. Ten ejaculates obtained by electroejaculation were diluted and stored at 5°C for 72 h.
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