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涉及阿片受体的神经通路对垂体激素应激反应缺乏调节作用。

Lack of modulation of pituitary hormone stress response by neural pathways involving opiate receptors.

作者信息

Spiler I J, Molitch M E

出版信息

J Clin Endocrinol Metab. 1980 Mar;50(3):516-20. doi: 10.1210/jcem-50-3-516.

Abstract

To evaluate the role of the opiate-like peptidergic pathways in modulating the pituitary hormone response to stress, we measured the GH, PRL, and cortisol responses to hypoglycemia and exercise in normal subjects with and without pretreatment with naloxone, given in the centrally active dose of 0.4 mg iv. Basal serum levels of GH, PRL, and cortisol were not changed significantly by prior naloxone administration. The maximum incremental response of GH to exercise was significantly blunted (13.1 +/- 1.6 vs. 6.0 +/- 1.4; P less than 0.001) by prior naloxone administration. Pretreatment with naloxone did not affect the responses of GH, PRL, or cortisol to hypoglycemia or the PRL response to L-dopa. On the basis of these studies we conclude that the opiate-like peptidergic pathways are not important in the regulation of basal levels of GH, PRL, and cortisol and have only a modest modulating influence on the stress-induced release of the hormones, which may be obscured in the face of severe stress.

摘要

为评估阿片样肽能通路在调节垂体激素对应激反应中的作用,我们测定了正常受试者在静脉注射0.4mg中枢活性剂量纳洛酮预处理前后,对低血糖和运动的生长激素(GH)、催乳素(PRL)及皮质醇反应。预先给予纳洛酮后,GH、PRL及皮质醇的基础血清水平无显著变化。预先给予纳洛酮显著减弱了运动引起的GH最大增量反应(分别为13.1±1.6与6.0±1.4;P<0.001)。纳洛酮预处理不影响GH、PRL或皮质醇对低血糖的反应,也不影响PRL对左旋多巴的反应。基于这些研究,我们得出结论:阿片样肽能通路在调节GH、PRL和皮质醇基础水平方面并不重要,对激素应激诱导释放仅有适度调节作用,在严重应激情况下这种作用可能被掩盖。

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