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在大鼠视前区/下丘脑前部微量注射甲硫氨酸脑啡肽酰胺后体温和代谢率的变化

Changes in body temperature and metabolic rate following microinjection of Met-enkephalinamide in the preoptic/anterior hypothalamus of rats.

作者信息

Stanton T L, Sartin N F, Beckman A L

出版信息

Regul Pept. 1985 Nov 28;12(4):333-43. doi: 10.1016/0167-0115(85)90177-6.

DOI:10.1016/0167-0115(85)90177-6
PMID:3867098
Abstract

The effects of Met-enkephalinamide (MET-ENKamide) on brain temperature (Tb) and metabolic rate (MR) were assessed following direct administration into the preoptic/anterior hypothalamus (PO/AH) of freely moving rats. Bilateral microinjections of saline or MET-ENKamide (1-25 micrograms/microliter) were delivered through cannula guide tubes previously implanted in nine animals. Thiorphan, an enkephalinase inhibitor, was microinjected into the PO/AH of two of the animals. All injections were made remotely at an ambient temperature of 22 +/- 1 degree C in a volume of 1 microliter. Measurements of Tb (via a brain-dwelling thermistor) and MR were recorded continuously. The ability of naloxone to antagonize the effects of MET-ENKamide was investigated by fashioning a double-barreled injection cannula to fit within each guide tube; 1 microliter of saline or naloxone (1-10 micrograms) was delivered bilaterally into the PO/AH followed by 1 microliter of MET-ENKamide (25 micrograms) 5-10 min later. PO/AH administration of MET-ENKamide (1-25 micrograms) produced dose-dependent increases in Tb preceded by dose-dependent increases in MR, with a characteristic time course of approximately 30 min. Naloxone antagonized the rise in Tb and MR, either partially or completely, depending on dose. When administered alone, naloxone had no effect on Tb or MR. Microinjection of thiorphan (10 micrograms) into the PO/AH evoked increases in Tb and MR that were similar to those responses induced by MET-ENKamide. These results support a role for endogenous Met-enkephalin in the regulation of Tb in the rat.

摘要

在自由活动的大鼠视前区/下丘脑前部(PO/AH)直接注射甲硫脑啡肽酰胺(MET-ENKamide)后,评估其对脑温(Tb)和代谢率(MR)的影响。通过先前植入9只动物体内的套管引导管进行双侧微量注射生理盐水或MET-ENKamide(1 - 25微克/微升)。将脑啡肽酶抑制剂硫磷酰胺微量注射到其中2只动物的PO/AH中。所有注射均在22±1℃的环境温度下以1微升的体积远程进行。连续记录Tb(通过脑内热敏电阻)和MR的测量值。通过制作适合每个引导管的双管注射套管来研究纳洛酮拮抗MET-ENKamide作用的能力;双侧向PO/AH注射1微升生理盐水或纳洛酮(1 - 10微克),5 - 10分钟后再注射1微升MET-ENKamide(25微克)。向PO/AH注射MET-ENKamide(1 - 25微克)会导致Tb剂量依赖性升高,之前MR也呈剂量依赖性升高,其特征性时间进程约为30分钟。纳洛酮根据剂量部分或完全拮抗Tb和MR的升高。单独给药时,纳洛酮对Tb或MR无影响。向PO/AH微量注射硫磷酰胺(10微克)会引起Tb和MR升高,类似于MET-ENKamide诱导的反应。这些结果支持内源性甲硫脑啡肽在大鼠Tb调节中的作用。

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