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参与体温过高的前列腺素和下丘脑神经递质受体:一项批判性评估。

Prostaglandins and hypothalamic neurotransmitter receptors involved in hyperthermia: a critical evaluation.

作者信息

Simpson C W, Ruwe W D, Myers R D

机构信息

Division of Molecular Biology and Biochemistry, University of Missouri, Kansas City 64108.

出版信息

Neurosci Biobehav Rev. 1994 Spring;18(1):1-20. doi: 10.1016/0149-7634(94)90033-7.

Abstract

The role of a prostaglandin of the E series (PGE) in the hypothalamic mechanisms underlying a fever continues to be controversial. This paper reviews the historical literature and current findings on the central action of the PGEs on body temperature (Tb). New experiments were undertaken to examine the local effect of muscarinic, nicotinic, serotonergic, alpha-adrenergic, or beta-adrenergic receptor antagonists at hypothalamic sites where PGE1 caused a rise in Tb of the primate. Guide tubes for microinjection were implanted stereotaxically above sites in and around the anterior hypothalamic, preoptic area (AH/POA) of male Macaque monkeys. Following postoperative recovery, 30-100 ng of PGE1 was micro-injected unilaterally in a volume of 1.0-1.5 microliter at sites in the AH/POA to evoke a rise in Tb, and once identified, pretreated with a receptor antagonist. PGE1 hyperthermia was significantly reduced by microinjections of the muscarinic and nicotinic antagonists, atropine, or mecamylamine, at PGE1 reactive sites in the AH/POA. The serotonergic antagonist, methysergide, injected at PGE1 sensitive sites in the ventromedial hypothalamus also attenuated the rise in Tb. However, the 5-HT reuptake blocker, fluoxetine, and the beta-adrenergic receptor antagonist, propranolol, injected in the AH/POA failed to alter the PGE1 hyperthermia. In contrast, the alpha-adrenergic antagonist, phentolamine, potentiated the increase in Tb at all PGE1 reactive sites in the hypothalamus. An updated model is presented to explain how the concurrent actions of aminergic neurotransmitters acting on their respective receptors in the hypothalamus can interact with a PGE to elicit hyperthermia. Finally, an evaluation of the current literature including recent findings on macrophage inflammatory protein (MIP-1) supports the conclusion that a PGE in the brain is neither an obligatory nor essential factor for the expression of a pyrogen fever.

摘要

E 系列前列腺素(PGE)在发热相关下丘脑机制中的作用一直存在争议。本文回顾了关于 PGE 对体温(Tb)中枢作用的历史文献和当前研究结果。开展了新的实验,以研究毒蕈碱、烟碱、5-羟色胺、α-肾上腺素能或β-肾上腺素能受体拮抗剂在灵长类动物下丘脑部位对 PGE1 引起体温升高的局部影响。将用于微量注射的引导管立体定向植入雄性猕猴下丘脑前部、视前区(AH/POA)及其周围部位上方。术后恢复后,在 AH/POA 部位以 1.0 - 1.5 微升的体积单侧微量注射 30 - 100 纳克的 PGE1 以引起体温升高,一旦确定部位,就用受体拮抗剂进行预处理。在 AH/POA 中 PGE1 反应部位微量注射毒蕈碱和烟碱拮抗剂阿托品或美加明,可显著降低 PGE1 引起的体温升高。在下丘脑腹内侧 PGE1 敏感部位注射 5-羟色胺拮抗剂麦角新碱也可减弱体温升高。然而,在 AH/POA 中注射 5-羟色胺再摄取阻滞剂氟西汀和β-肾上腺素能受体拮抗剂普萘洛尔未能改变 PGE1 引起体温升高的作用。相反,α-肾上腺素能拮抗剂酚妥拉明增强了下丘脑所有 PGE1 反应部位的体温升高。本文提出了一个更新的模型,以解释作用于下丘脑各自受体的胺能神经递质的协同作用如何与 PGE 相互作用引发体温升高。最后,对包括巨噬细胞炎性蛋白(MIP-1)最新研究结果在内的当前文献进行评估,支持以下结论:脑内的 PGE 既不是致热原性发热表达的必要因素也不是关键因素。

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