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δ和κ阿片受体在促甲状腺激素释放激素抗失血性休克特性中的重要性。

The importance of delta and kappa opioid receptors in the property of thyrotropin-releasing hormone against hemorrhagic shock.

作者信息

Liu L M, Hu D Y, Chen H S, Lu R Q, Yan W

机构信息

Research Institute of Surgery, Daping Hospital, Chongqing, People's Republic of China.

出版信息

Shock. 1997 Jan;7(1):60-4. doi: 10.1097/00024382-199701000-00008.

Abstract

Many studies have demonstrated that thyrotropin-releasing hormone (TRH) produces various beneficial effects in the treatment of shock. TRH has been proposed to reverse the cardiovascular depression of endogenous opioid peptides. Nevertheless, it remains unknown whether opioid receptors are truly involved in this process. We designed experiments to study the importance of delta and kappa opioid receptors in the beneficial effects of TRH in hemorrhagic shock in rabbits and on opiate receptors following hemorrhagic shock in rats. The results indicated that TRH (50 micrograms, i.c.v.) significantly improved the mean arterial pressure (MAP), left ventricular systolic pressure (LVSP), and the maximal rate of ventricular systolic pressure changes (+/- dp/dtmax) during hemorrhagic shock in rabbits. This TRH effect was abolished by pretreatment with ICI174,864 (50 micrograms, i.c.v.), a highly selective delta opioid receptor antagonist, but not by pretreatment with nor-binaltorphimine (Nor-BNI, 50 micrograms, i.c.v.), a highly selective kappa opioid receptor antagonist. The maximal binding capacity (Bmax) of brain delta and kappa opioid receptors significantly increased following hemorrhagic shock, but the receptor affinity (Kd) did not change. TRH (5 mg/kg, i.v.) decreased the number (Bmax) of brain delta opioid receptors significantly, but it did not influence the receptor affinity. TRH did not influence the Bmax or affinity of brain kappa opioid receptors. These findings suggest that opioid receptors play an important role in mediating the antishock property of TRH. TRH-induced down-regulation of the number of brain opioid receptors may be one of the important mechanisms by which TRH exercises its protective effects in the treatment of shock.

摘要

许多研究表明,促甲状腺激素释放激素(TRH)在休克治疗中产生多种有益作用。有人提出TRH可逆转内源性阿片肽引起的心血管抑制。然而,阿片受体是否真的参与这一过程仍不清楚。我们设计了实验来研究δ和κ阿片受体在TRH对兔失血性休克的有益作用以及对大鼠失血性休克后阿片受体的重要性。结果表明,TRH(50微克,脑室内注射)显著改善了兔失血性休克期间的平均动脉压(MAP)、左心室收缩压(LVSP)以及心室收缩压变化的最大速率(±dp/dtmax)。ICI174,864(50微克,脑室内注射),一种高度选择性的δ阿片受体拮抗剂,预处理可消除TRH的这种作用,但高度选择性的κ阿片受体拮抗剂去甲丙氨酰吗啡(Nor-BNI,50微克,脑室内注射)预处理则无此作用。失血性休克后,脑δ和κ阿片受体的最大结合容量(Bmax)显著增加,但受体亲和力(Kd)未改变。TRH(5毫克/千克,静脉注射)显著降低了脑δ阿片受体的数量(Bmax),但不影响受体亲和力。TRH不影响脑κ阿片受体的Bmax或亲和力。这些发现表明,阿片受体在介导TRH的抗休克特性中起重要作用。TRH诱导的脑阿片受体数量下调可能是TRH在休克治疗中发挥保护作用的重要机制之一。

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