Preclinical study reveals that anterior hypothalamic projections to the periaqueductal gray drive mating rejection in females, highlighting circuit mechanisms tied to fertility cycles.
Selecting an appropriate behavioral response according to one’s internal state is essential for well-being. Across the reproductive cycle, fluctuating levels of sex hormones align female behavior with reproductive capacity by modulating neuronal circuits that express hormone receptors. Sex hormone receptor-expressing neurons present along the anterior-posterior axis of the ventrolateral region of the ventromedial hypothalamus (VMHvl) are key regulators of female sexual behavior. While posterior progesterone receptor-expressing neurons of the VMHvl (pVMHvl PR+ ) are fundamental for female sexual receptivity during the receptive phase of the reproductive cycle, we have recently shown that anterior VMHvl PR+ (aVMHvl PR+ ) neurons are involved in rejection behavior when non-receptive. Here, we mapped the connectional architecture of aVMHvl PR+ neurons using viral tracing approaches. As expected, these neurons strongly project to several hypothalamic areas. Furthermore, consistent with previous reports, we show that aVMHvl PR+ neurons robustly project to several columns of the periaqueductal gray (PAG) along its anterior-posterior axis. Artificial activation of aVMHvl PR+ somas selectively recruits the dorsomedial PAG (dmPAG). Optogenetic activation of aVMHvl PR+ axons in the dmPAG partially recapitulates the rejection phenotype observed upon activation of aVMHvl PR+ somas, increasing the rate of rejections in receptive females. These findings reveal a putative pathway regulating female rejection behavior within a more complex circuit, ensuring that mating does not occur during non fertile periods.
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Dias et al. (2026) studied this question.
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