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共存的神经肽 FF 和促性腺激素释放激素 3 协同调节雄性性行为。

Co-existing Neuropeptide FF and Gonadotropin-Releasing Hormone 3 Coordinately Modulate Male Sexual Behavior.

机构信息

Department of Biological Sciences, Graduate School of Science, the University of Tokyo, Tokyo, Japan.

Department of Anatomy, St. Marianna University School of Medicine, Kanagawa, Japan.

出版信息

Endocrinology. 2022 Feb 1;163(2). doi: 10.1210/endocr/bqab261.

Abstract

Animals properly perform sexual behaviors by using multiple sensory cues. However, neural mechanisms integrating multiple sensory cues and regulating motivation for sexual behaviors remain unclear. Here, we focused on peptidergic neurons, terminal nerve gonadotropin-releasing hormone (TN-GnRH) neurons, which receive inputs from various sensory systems and co-express neuropeptide FF (NPFF) in addition to GnRH. Our behavioral analyses using knockout medaka of GnRH (gnrh3) and/or NPFF (npff) demonstrated that some sexual behavioral repertoires were delayed, not disrupted, in gnrh3 and npff single knockout males, while the double knockout appeared to alleviate the significant defects that were observed in single knockouts. We also found anatomical evidence to show that both neuropeptides modulate the sexual behavior-controlling brain areas. Furthermore, we demonstrated that NPFF activates neurons in the preoptic area via indirect pathway, which is considered to induce the increase in motivation for male sexual behaviors. Considering these results, we propose a novel mechanism by which co-existing peptides of the TN-GnRH neurons, NPFF, and GnRH3 coordinately modulate certain neuronal circuit for the control of behavioral motivation. Our results may go a long way toward understanding the functional significance of peptidergic neuromodulation in response to sensory information from the external environments.

摘要

动物通过使用多种感官线索来正确执行性行为。然而,整合多种感官线索并调节性行为动机的神经机制仍不清楚。在这里,我们专注于肽能神经元,终器神经促性腺激素释放激素(TN-GnRH)神经元,其除了 GnRH 之外还接收来自各种感觉系统的输入并共同表达神经肽 FF(NPFF)。我们使用 GnRH(gnrh3)和/或 NPFF(npff)敲除斑马鱼的行为分析表明,gnrh3 和 npff 单敲除雄性的一些性行为模式被延迟,而不是被破坏,而双敲除似乎减轻了单敲除中观察到的显著缺陷。我们还发现了解剖学证据表明,这两种神经肽都调节控制性行为的大脑区域。此外,我们证明 NPFF 通过间接途径激活视前区的神经元,这被认为会增加雄性性行为的动机。考虑到这些结果,我们提出了一个新的机制,即 TN-GnRH 神经元、NPFF 和 GnRH3 共存的肽共同协调调节某些神经元回路以控制行为动机。我们的研究结果可能有助于理解肽能神经调制对来自外部环境的感觉信息的功能意义。

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