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乌拉坦麻醉成年雄性大鼠中肾上腺素能和多巴胺能对生长激素分泌的控制

Adrenergic and dopaminergic control of growth hormone secretion in urethan anesthetized adult male rats.

作者信息

Ruch W, Marbach P, Jaton A L, Bucher B, Doepfner W

出版信息

Horm Res. 1978;9(4):208-24. doi: 10.1159/000178915.

Abstract

The effects of drugs which interfere with alpha-adrenergic and dopaminergic mechanisms, involved in GH and PRL secretion, have been analyzed in urethane anesthetized rats. Clonidine induced a dose-dependent release of GH (0.0032--0.1 mg/kg i.v.) as well as of PRL (0.032--1.0 mg/kg i.v.). The lowest dose of clonidine, when given into the third ventricle, provoked a very pronounced release of GH. Phentolamine, given intravenously, inhibited the clonidine-induced GH release in a dose-dependnet manner. L-Dopa administered intravenously and apomorphine administered intravenously or intraventricularly did not affect basal secretion of GH bu- produced a dose-dependnet inhibition of clonidine-induced GH release. Pimozide did not change basal GH secretion. Furthermore pimozide did not attenuate the inhibition of clonidine-induced GH secretion seen after apomorphine administration, however, it completely reversed apomorphine-induced PRL inhibition. These findings demonstrate that an alpha-adrenoceptor-mediated stimulatory mechanism is involved in GH and PRL secretion. An inhibitory dopaminergic mechanism is confirmed for PRL secretion and suggested for GH secretion.

摘要

在氨基甲酸乙酯麻醉的大鼠中,分析了干扰参与生长激素(GH)和催乳素(PRL)分泌的α-肾上腺素能和多巴胺能机制的药物的作用。可乐定静脉注射时(0.0032 - 0.1毫克/千克)可引起GH以及PRL的剂量依赖性释放(0.032 - 1.0毫克/千克)。当将最低剂量的可乐定注入第三脑室时,会引发非常明显的GH释放。静脉注射酚妥拉明以剂量依赖性方式抑制可乐定诱导的GH释放。静脉注射左旋多巴以及静脉内或脑室内注射阿扑吗啡不影响GH的基础分泌,但会对可乐定诱导的GH释放产生剂量依赖性抑制。匹莫齐特不改变GH基础分泌。此外,匹莫齐特不会减弱阿扑吗啡给药后对可乐定诱导的GH分泌的抑制作用,然而,它完全逆转了阿扑吗啡诱导的PRL抑制。这些发现表明,α-肾上腺素能受体介导的刺激机制参与了GH和PRL的分泌。证实了多巴胺能抑制机制参与PRL分泌,并提示其参与GH分泌。

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