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首页> 外文期刊>Journal of neuroendocrinology >Interaction between norepinephrine, oxytocin, and nitric oxide in the stimulation of gonadotropin-releasing hormone release from proestrous rat Basal hypothalamus explants.
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Interaction between norepinephrine, oxytocin, and nitric oxide in the stimulation of gonadotropin-releasing hormone release from proestrous rat Basal hypothalamus explants.

机译:去甲肾上腺素,催产素和一氧化氮之间的相互作用刺激促性腺激素大鼠下丘脑外植体释放促性腺激素释放激素。

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摘要

Abstract In the proestrous female rat, norepinephrine, oxytocin and nitric oxide (NO) all participate in the regulation of the preovulatory gonadotropin-releasing hormone (GnRH) surge. Recent studies from our laboratory have demonstrated that oxytocin induces dose-dependent release of GnRH from proestrous basal hypothalamus explants. The present studies were undertaken to determine whether norepinephrine could also stimulate GnRH release from similar explants, to identify the receptors responsible for this effect and to investigate interactions between norepinephrine, oxytocin and NO. Norepinephrine significantly stimulated GnRH release from proestrous basal hypothalamus explants, and coadministration of the alpha(1)-adrenergic antagonist prazosin blocked this effect. Combined administration of oxytocin and norepinephrine stimulated significantly more GnRH release than either drug alone, and this stimulation was blocked by inhibition of NO synthase, or by an oxytocin receptor antagonist. NO production was measured from the same samples using a modified Griess reaction. Oxytocin, but not norepinephrine, significantly increased NO production, as did norepinephrine and oxytocin in combination. Oxytocin receptor antagonist administration attenuated the stimulation of NO production by norepinephrine/oxytocin. These results demonstrate for the first time that oxytocin and norepinephrine dramatically stimulate GnRH release from basal hypothalamus explants harvested on the afternoon of proestrus, and indicate that this involves oxytocin receptor and NO-dependent mechanisms.
机译:摘要在雌性雌性大鼠中,去甲肾上腺素,催产素和一氧化氮(NO)均参与排卵前促性腺激素释放激素(GnRH)激增的调节。我们实验室的最新研究表明,催产素可诱导前体基底下丘脑外植体中GnRH的剂量依赖性释放。进行本研究以确定去甲肾上腺素是否也可以刺激类似外植体释放GnRH,确定引起这种作用的受体,并研究去甲肾上腺素,催产素和NO之间的相互作用。去甲肾上腺素显着刺激GnRH释放从发情的基础下丘脑外植体,和α(1)-肾上腺素能拮抗剂哌唑嗪的共同给药阻止了这种作用。催产素和去甲肾上腺素的联合给药比单独使用任何一种药物刺激的GnRH释放明显多,并且这种刺激被NO合酶或催产素受体拮抗剂的抑制所阻断。使用改良的Griess反应从相同的样品测量NO的产生。催产素而不是去甲肾上腺素不能显着增加NO的产生,就像去甲肾上腺素和催产素联合使用一样。催产素受体拮抗剂的给药减弱了去甲肾上腺素/催产素对NO产生的刺激作用。这些结果首次证明催产素和去甲肾上腺素极大地刺激了从发情期下午收获的基底下丘脑外植体释放GnRH,并表明这涉及催产素受体和NO依赖性机制。

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