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阿片能对甲状腺活动的调节:可能对5-羟色胺能系统产生干扰。

Opioidergic regulation of thyroid activity: possible interference with the serotonergic system.

作者信息

Rúzsás C, Mess B

出版信息

Psychoneuroendocrinology. 1983;8(1):89-94. doi: 10.1016/0306-4530(83)90044-6.

Abstract

Acute systemic administration of (D-Met2, pro5-NH2)-enkephalin (ENKamide), a very potent enkephalin analog, and of morphine not only diminished the basal levels of serum TSH under resting conditions, but also significantly reduced the enhanced serum TSH concentrations induced by goitrogen treatment or by bilateral thyroidectomy. Acute administration of opiates failed to inhibit the pituitary TSH response to exogenous TRH administration. The TSH release-inhibiting effect of ENKamide was reversed by pretreatment with the serotonin synthesis inhibitor, para-chlorophenylalanine (pCPA) or with the central serotonin receptor blocker, metergoline. These results furnish evidence in favour of the following concepts: (a) opioid compounds equally influence the tonic release of the TRH-TSH system under resting conditions, and also suppress the reactive changes of this circuit following specific loads, leading to an activation of this system; (b) opioids do not act directly at the pituitary level in inhibiting TSH secretion, but rather seem to suppress the release of TRH from the hypothalamus; (c) they may exert their inhibitory effect on the activity of the TRH-TSH-thyroid system by increasing the activity of the central nervous serotonergic system.

摘要

强效脑啡肽类似物(D-蛋氨酸²,脯氨酸⁵-氨基)-脑啡肽(ENKamide)和吗啡的急性全身给药,不仅降低了静息状态下血清促甲状腺激素(TSH)的基础水平,还显著降低了由致甲状腺肿药物治疗或双侧甲状腺切除所诱导的血清TSH浓度升高。阿片类药物的急性给药未能抑制垂体对外源性促甲状腺激素释放激素(TRH)给药的TSH反应。用5-羟色胺合成抑制剂对氯苯丙氨酸(pCPA)或中枢5-羟色胺受体阻滞剂麦角林预处理后,可逆转ENKamide的TSH释放抑制作用。这些结果为以下概念提供了证据:(a)阿片类化合物在静息状态下同样影响TRH-TSH系统的紧张性释放,并且还抑制该回路在特定负荷后的反应性变化,导致该系统的激活;(b)阿片类药物在抑制TSH分泌时并非直接作用于垂体水平,而是似乎抑制了下丘脑TRH的释放;(c)它们可能通过增加中枢神经5-羟色胺能系统的活性,对TRH-TSH-甲状腺系统的活性发挥抑制作用。

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