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儿茶酚胺合成抑制剂和肾上腺素能受体拮抗剂对束缚诱导的促黄体生成素释放的影响。

Effects of catecholamine synthesis inhibitors and adrenergic receptor antagonists on restraint-induced LH release.

作者信息

Martín A I, Fernández-Ruiz J, López-Calderón A

机构信息

Departamento de Fisiologia, Facultad de Medicina, Universidad Complutense, Madrid, Spain.

出版信息

J Endocrinol. 1995 Mar;144(3):511-5. doi: 10.1677/joe.0.1440511.

Abstract

Acute stress is known to increase LH secretion and the release of central norepinephrine (NE) in intact rats. Studies were performed to analyse the ole of catecholamines in acute stress-induced LH release in male rats. Injection of alpha-methyl-p-tyrosine (alpha MPT) and diethyldithiocarbamate (DDC), catecholamine synthesis inhibitors, significantly decreased both hypothalamic concentration of NE and serum LH. Restraint for 30 min evoked an increase in serum LH in saline-treated rats, whereas alpha MPT and DDC administration blocked the stress-induced LH release. The effects of alpha 1-, alpha 2- and beta-adrenoreceptor antagonists on the LH response to restraint stress were also studied. Propranolol treatment did not modify serum LH in either unstressed or stressed rats. The two alpha-adrenergic receptor antagonists prazosin and yohimbine prevented the restraint-induced LH release; however, prazosin but not yohimbine significantly decreased the serum concentration of LH in unstressed rats. These data suggest that the acute stress-induced increase in LH secretion is mediated through the activation of alpha 2-adrenergic receptors.

摘要

已知急性应激会增加完整大鼠体内促黄体生成素(LH)的分泌以及中枢去甲肾上腺素(NE)的释放。本研究旨在分析儿茶酚胺在雄性大鼠急性应激诱导的LH释放中的作用。注射儿茶酚胺合成抑制剂α-甲基-对-酪氨酸(α-MPT)和二乙基二硫代氨基甲酸盐(DDC),可显著降低下丘脑NE浓度和血清LH水平。对生理盐水处理的大鼠束缚30分钟可使血清LH升高,而给予α-MPT和DDC则可阻断应激诱导的LH释放。还研究了α1-、α2-和β-肾上腺素能受体拮抗剂对LH对应激束缚反应的影响。普萘洛尔处理对未应激和应激大鼠的血清LH均无影响。两种α-肾上腺素能受体拮抗剂哌唑嗪和育亨宾可阻止束缚诱导的LH释放;然而,哌唑嗪而非育亨宾可显著降低未应激大鼠的血清LH浓度。这些数据表明,急性应激诱导的LH分泌增加是通过α2-肾上腺素能受体的激活介导的。

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