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Opposite-sex attraction in male mice requires testosterone-dependent regulation of adult olfactory bulb neurogenesis

机译:在雄性小鼠中相反的性吸引需要成年嗅球神经发生的睾丸激素依赖性调节

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摘要

Opposite-sex attraction in most mammals depends on the fine-tuned integration of pheromonal stimuli with gonadal hormones in the brain circuits underlying sexual behaviour. Neural activity in these circuits is regulated by sensory processing in the accessory olfactory bulb (AOB), the first central station of the vomeronasal system. Recent evidence indicates adult neurogenesis in the AOB is involved in sex behaviour; however, the mechanisms underlying this function are unknown. By using Semaphorin 7A knockout (Sema7A ko) mice, which show a reduced number of gonadotropin-releasing-hormone neurons, small testicles and subfertility, and wild-type males castrated during adulthood, we demonstrate that the level of circulating testosterone regulates the sex-specific control of AOB neurogenesis and the vomeronasal system activation, which influences opposite-sex cue preference/attraction in mice. Overall, these data highlight adult neurogenesis as a hub for the integration of pheromonal and hormonal cues that control sex-specific responses in brain circuits.
机译:在大多数哺乳动物中,对性吸引取决于对性行为引起的脑回路中信息素刺激与性腺激素的微调整合。这些回路中的神经活动是通过感觉嗅球(AOB)(犁鼻系统的第一个中心站)的感觉处理来调节的。最近的证据表明,AOB中的成人神经发生与性行为有关。但是,此功能的基础机制尚不清楚。通过使用Semaphorin 7A基因敲除(Sema7A ko)小鼠,这些小鼠的促性腺激素释放激素神经元数量减少,小睾丸和亚生育力降低,并且成年期cast割的野生型雄性小鼠,我们证明了循环睾丸激素的水平调节着性AOB神经发生和犁鼻系统激活的特异性控制,这会影响小鼠的异性提示偏好/吸引力。总体而言,这些数据突出了成人神经发生,将其作为控制脑回路中性别特异性反应的信息素和激素信息整合的枢纽。

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