首页> 外文期刊>Behavioural Brain Research: An International Journal >Evidence that the effect of melanocortins on female sexual behavior in preoptic area is mediated by the MC3 receptor; Participation of nitric oxide.
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Evidence that the effect of melanocortins on female sexual behavior in preoptic area is mediated by the MC3 receptor; Participation of nitric oxide.

机译:黑色素皮质素对视前区女性性行为的影响是由MC3受体介导的证据;一氧化氮的参与。

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摘要

alpha-MSH is involved in reproductive processes and can regulate the expression of lordosis, an important component of female reproductive behavior in rats and many other species. In this study, we investigated the effects of MSH peptides on lordosis behavior when injected in medial preoptic area (POA) of ovariectomised rats primed with estradiol. The results show an increase in lordotic activity after bilateral administration of alpha-MSH and gamma-MSH. Interestingly, the treatment with the MC4 receptor antagonist HS014 did not block the stimulatory effect of alpha-MSH. Moreover, the injection of HS014 did not itself modify the lordosis quotient. Nitric oxide has been suggested to play a crucial role in the regulation of lordosis behavior via stimulation of guanylyl cyclase to synthesize cGMP. In order to determine the participation of NO in the effect of the melanocortins, another group of rats were treated with l-NAME, an inhibitor of NOS, alone or 15min before the injection of alpha-MSH or gamma-MSH. The injection of l-NAME into the POA of E-primed rats 15min before the test for sexual receptivity did not modify significantly the lordosis quotient at the two doses examined. The treatment with l-NAME at the lowest dose completely abolished the stimulatory effect of alpha-MSH and gamma-MSH on sexual behavior. The results indicate that the effects of MSH peptides on female sexual behavior in this area are mediated through specific MC receptor, that could be the MC3 receptor and that NO mediates the melanocortins effects.
机译:alpha-MSH参与生殖过程,可以调节脊柱前凸的表达,脊柱前凸是大鼠和许多其他物种女性生殖行为的重要组成部分。在这项研究中,我们调查了注射雌二醇致卵巢切除大鼠的内侧视前区(POA)中MSH肽对脊柱前凸行为的影响。结果表明,双侧服用α-MSH和γ-MSH后脊索动物活动增加。有趣的是,用MC4受体拮抗剂HS014进行的治疗并未阻断α-MSH的刺激作用。而且,注射HS014本身并不能改变脊柱前凸商。一氧化氮被认为通过刺激鸟苷酸环化酶合成cGMP在脊柱前凸行为的调节中起关键作用。为了确定NO是否参与黑皮质素的作用,另一组大鼠在注射α-MSH或γ-MSH之前单独或15分钟用NOS抑制剂l-NAME治疗。在进行性感受力测试之前15分钟,将l-NAME注入E-致敏大鼠的POA中,在两种剂量下均未显着改变脊柱前凸的商数。用最低剂量的l-NAME治疗完全消除了α-MSH和γ-MSH对性行为的刺激作用。结果表明,MSH肽对该区域女性性行为的影响是通过特定的MC受体介导的,该受体可能是MC3受体,而NO则介导了黑皮质素的作用。

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