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Orexin mediates initiation of sexual behavior in sexually naive male rats, but is not critical for sexual performance.

机译:食欲素介导天真的雄性大鼠性行为的启动,但对性行为并不重要。

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The hypothalamic neuropeptide orexin mediates arousal, sleep, and naturally rewarding behaviors, including food intake. Male sexual behavior is altered by orexin receptor-1 agonists or antagonists, suggesting a role for orexin-A in this naturally rewarding behavior. However, the specific role of endogenous orexin-A or B in different elements of male sexual behavior is currently unclear. Therefore, the current studies utilized markers for neural activation and orexin cell-specific lesions to test the hypothesis that orexin is critical for sexual motivation and performance in male rats. First, cFos expression in orexin neurons was demonstrated following presentation of a receptive or non-receptive female without further activation by different elements of mating. Next, the functional role of orexin was tested utilizing orexin-B conjugated saporin, resulting in orexin cell body lesions in the hypothalamus. Lesions were conducted in sexually naive males and subsequent sexual behavior was recorded during four mating trials. Lesion males showed shortened latencies to mount and intromit during the first, but not subsequent mating trials, suggesting lesions facilitated initiation of sexual behavior in sexually naive, but not experienced males. Likewise, lesions did not affect sexual motivation in experienced males, determined by runway tests. Finally, elevated plus maze tests demonstrated reduced anxiety-like behaviors in lesioned males, supporting a role for orexin in anxiety associated with initial exposure to the female in naive animals. Overall, these findings show that orexin is not critical for male sexual performance or motivation, but may play a role in arousal and anxiety related to sexual behavior in naive animals.
机译:下丘脑神经肽食欲肽介导唤醒,睡眠和自然有益的行为,包括食物摄入。男性的性行为被orexin受体1激动剂或拮抗剂所改变,表明orexin-A在这种自然有益的行为中起作用。但是,目前尚不清楚内源性orexin-A或B在男性性行为的不同元素中的具体作用。因此,当前的研究利用神经激活标记和orexin细胞特异性病变来检验orexin对雄性大鼠性动机和性行为至关重要的假说。首先,在出现雌性或非雌性雌性动物后,通过不同交配要素的进一步激活,证明了orexin神经元中的cFos表达。接下来,利用orexin-B结合的saporin测试了orexin的功能作用,导致下丘脑中orexin细胞的身体受损。在未接受过性行为的男性中进行病变,并在四次交配试验中记录了随后的性行为。病变男性在第一次但不是随后的交配试验中显示出缩短的坐骑和内向潜伏期,这表明病变促进了天真的性行为发起,但没有经验的男性。同样,通过跑道测试确定,病变也不会影响有经验的男性的性动机。最后,高架迷宫测试证明了患病雄性动物的焦虑样行为减少,这支持了食欲素在与初次暴露于母体的雌性动物相关的焦虑中的作用。总体而言,这些发现表明,食欲素对雄性性行为或性动机并不重要,但可能在幼稚动物的性行为引起的唤醒和焦虑中起作用。

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