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下丘脑前部损伤增强氯丙嗪诱导的体温过低。

The enhancement of chlorpromazine-induced hypothermia by lesions in the anterior hypothalamus.

作者信息

Chai C Y, Lin M T

出版信息

Br J Pharmacol. 1977 Sep;61(1):77-82. doi: 10.1111/j.1476-5381.1977.tb09741.x.

DOI:10.1111/j.1476-5381.1977.tb09741.x
PMID:912209
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1667651/
Abstract

1 Administration of chlorpromazine (Cpz), either systemically or centrally, to unanaesthetized rats at an environmental temperature of 23 degrees C caused dose-dependent hypothermia. 2 In order to achieve equivalent hypothermia, intraventricular administration required a total dose of 20 microgram Cpz and and intraperitoneal administration a dose of 9.7 mg/kg body weight. Accordingly, the dose-ratio between intraventricular and intraperitoneal administration was 1 to 110. Cpz apparently exerts its hypothermic effect by acting directly on central nervous structures rather than through peripheral sites. 3 Cpz-induced hypothermia was potentiated by preoptic anterior hypothalamic (POAH) lesions but not by lesions of the ventromedial nucleus (VMN) of the hypothalamus. It was found that Cpz induced hypothermia most readily in rats with large POAH lesions (-10.4 degrees C), less so in rats with spinal lesions (-5.5 degrees C) at least with control rats (-2.9 degrees C).

摘要
  1. 在环境温度为23摄氏度时,给未麻醉的大鼠全身或中枢给予氯丙嗪(Cpz)会引起剂量依赖性体温过低。2. 为了达到同等程度的体温过低,脑室内给药需要20微克Cpz的总剂量,腹腔内给药需要9.7毫克/千克体重的剂量。因此,脑室内给药与腹腔内给药的剂量比为1比110。Cpz显然是通过直接作用于中枢神经结构而非外周部位来发挥其降温作用的。3. 视前区下丘脑前部(POAH)损伤会增强Cpz诱导的体温过低,但下丘脑腹内侧核(VMN)损伤则不会。研究发现,Cpz在POAH损伤较大的大鼠中最容易诱导体温过低(-10.4摄氏度),在脊髓损伤的大鼠中次之(-5.5摄氏度),至少与对照大鼠(-2.9摄氏度)相比是这样。

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本文引用的文献

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THE INFLUENCE OF CHLORPROMAZINE ON PHYSICAL AND CHEMICAL MECHANISMS OF TEMPERATURE REGULATION IN THE RAT.氯丙嗪对大鼠体温调节物理和化学机制的影响
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[Pharmacodynamic properties of 3-chloro-10-(3-dimethylaminopropyl)-phenothiazine hydrochloride (R.P. 4560); experimental study of a new substance used in potentialized anesthesia and in artificial hibernation].[盐酸3-氯-10-(3-二甲基氨基丙基)-吩噻嗪(R.P. 4560)的药效学特性;一种用于强化麻醉和人工冬眠的新物质的实验研究]
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