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纳曲酮诱导大鼠体温过低。

Naltrexone-induced hypothermia in the rat.

作者信息

Ary M, Chesarek W, Sorensen S M, Lomax P

出版信息

Eur J Pharmacol. 1976 Oct;39(2):215-20. doi: 10.1016/0014-2999(76)90129-1.

Abstract

Naltrexone, in relatively high doses, has been reported to cause a fall in body temperature in human ex-heroin addicts who had been abstinent for at least 6 weeks. The underlying mechanism of this hypothermic effect has been investigated in rats. The first consideration was that the temperature change was a reflection of delayed withdrawal but rats implanted with a morphine pellet 45 days earlier showed no significant change in temperature after a dose of naltrexone that caused marked withdrawal hypothermia in dependent rats implanted 3 days previously. A fall in core temperature was only induced in rats after doses of 80 and 160 mg/kg i.p. of naltrexone. Behavioral thermoregulatory studies revealed that the animals correct the falling body temperature by increased exposure to a radiant heat source indicating that the central thermostats had not been significantly affected by the drug. These data suggest that the major component in the hypothermic effect of naltrexone is activation of efferent heat loss pathways or peripheral heat loss mechanisms. Due to current suggestions that opiate receptors might represent the receptors for an endogenous transmitter the results are discussed in relation to this consideration. When compared to the sites and mechanism of action of opiates on thermoregulation the results with naltrexone lend little support to the hypothesis that the fall in temperature is due to displacement of an endogenous substance from central opiate receptors.

摘要

据报道,相对高剂量的纳曲酮会使戒毒至少6周的前海洛因成瘾者体温下降。已在大鼠身上研究了这种低温效应的潜在机制。首先考虑的是温度变化是延迟戒断的反映,但45天前植入吗啡丸的大鼠在给予一剂纳曲酮后体温没有显著变化,而3天前植入吗啡丸的依赖大鼠给予相同剂量的纳曲酮后出现了明显的戒断性体温过低。只有腹腔注射80和160mg/kg剂量的纳曲酮后,大鼠的核心体温才会下降。行为体温调节研究表明,动物通过增加暴露于辐射热源来纠正体温下降,这表明中枢恒温器未受到该药物的显著影响。这些数据表明,纳曲酮低温效应的主要成分是传出性散热途径或外周散热机制的激活。鉴于目前认为阿片受体可能代表内源性递质的受体,本文将结合这一观点对结果进行讨论。与阿片类药物对体温调节的作用部位和作用机制相比,纳曲酮的结果几乎无法支持体温下降是由于内源性物质从中枢阿片受体上被取代的假说。

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