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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >In vivo action of a new octadecaneuropeptide (ODN) antagonist on gonadotropin-releasing hormone gene expression in the male rat brain.
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In vivo action of a new octadecaneuropeptide (ODN) antagonist on gonadotropin-releasing hormone gene expression in the male rat brain.

机译:一种新的十八烯肽(ODN)拮抗剂对雄性大鼠大脑中促性腺激素释放激素基因表达的体内作用。

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摘要

It has been reported that several of the effects induced by octadecaneuropeptide (ODN) could be mediated by an activation of a metabotropic receptor. In order to investigate the role and mechanism of action of ODN in gonadotropin-releasing hormone (GnRH) neuron regulation, we studied the effects of the acute i.c.v. administration of ODN and of a new ODN antagonist to metabotropic receptor, cyclo(1-8)[Dleu(5)]OP, on GnRH mRNA expression as evaluated by in situ hybridization in castrated male rats. The administration of ODN produced a decrease in the hybridization signal while the administration of cyclo(1-8)[Dleu(5)]OP alone produced an 18% increase. When administrated concomitantly with ODN, the antagonist both inhibited the depressing effect of ODN and induced a 22% increase over the values detected in ODN-treated rats. The data suggest that the effect of ODN on GnRH mRNA expression might be mediated by interaction with metabotropic receptors.
机译:据报道,十八碳肽(ODN)诱导的几种作用可能是由代谢型受体的激活介导的。为了研究ODN在促性腺激素释放激素(GnRH)神经元调节中的作用和作用机理,我们研究了急性腹膜内毒素的作用。经去势雄性大鼠原位杂交评估,将ODN和一种新的ODN拮抗剂用于代谢型受体环(1-8)[Dleu(5)] OP对GnRH mRNA表达的影响。 ODN的使用产生了杂交信号的减少,而单独使用cyclo(1-8)[Dleu(5)] OP产生了18%的增加。当与ODN并用时,拮抗剂既抑制ODN的抑制作用,又比ODN处理的大鼠中检测到的值增加22%。数据表明ODN对GnRH mRNA表达的影响可能是通过与代谢型受体的相互作用介导的。

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