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褪黑素增强大鼠下丘脑5-HT(1A)受体的激活并导致体温过低。

Melatonin potentiates 5-HT(1A) receptor activation in rat hypothalamus and results in hypothermia.

作者信息

Lin Mao-Tsun, Chuang Jih-Ing

机构信息

Department of Medical Research, Chi-Mei Medical Center, Yung-Kang City, Tainan Hsien, Taiwan.

出版信息

J Pineal Res. 2002 Aug;33(1):14-9. doi: 10.1034/j.1600-079x.2002.01867.x.

Abstract

Effects of melatonin on both thermoregulatory responses and hypothalamic serotonin release were assessed in unanesthetized rats at three different ambient temperatures (Ta). Systemic administration of melatonin (30-120 mg/kg, i.p) caused a decrease in both colonic temperature and hypothalamic serotonin (5-HT) release in rats at both Ta 8 and 22 degrees C. The hypothermia was brought about by a decrease in metabolic rate at Ta 8 degrees C, whereas at Ta 22 degrees C the hypothermia was produced by both a decrease in metabolic rate and an increase in cutaneous temperature. However, in the heat (Ta 31 degrees C), neither thermoregulatory responses nor hypothalamic 5-HT release was affected by the same amount of administered melatonin. The melatonin-induced hypothermia and decreased 5-HT release in the hypothalamus were attenuated by selective depletion of brain 5-HT produced by intracerebroventricular injection of 5,7-dihydroxytryptamine. Furthermore, the melatonin-induced hypothermia was almost completely abolished by treatment with a 5-HT2A receptor agonist (DOI) or a 5-HT1A receptor antagonist [(-)-pindolol]. The data indicate that melatonin potentiates the 5-HT1A receptor activation in the hypothalamus and results in hypothermic effects which can be antagonized by the expected hyperthermic effect of DOI.

摘要

在三种不同环境温度(Ta)下,对未麻醉大鼠褪黑素对体温调节反应和下丘脑5-羟色胺释放的影响进行了评估。在8℃和22℃的Ta条件下,腹腔注射褪黑素(30 - 120mg/kg)会导致大鼠结肠温度和下丘脑5-羟色胺(5-HT)释放减少。在8℃的Ta条件下,体温过低是由代谢率降低引起的;而在22℃的Ta条件下,体温过低是由代谢率降低和皮肤温度升高共同导致的。然而,在高温(31℃的Ta)条件下,相同剂量的褪黑素既不影响体温调节反应,也不影响下丘脑5-HT释放。通过脑室内注射5,7-二羟色胺选择性耗尽脑内5-HT,可减弱褪黑素诱导的体温过低和下丘脑5-HT释放减少。此外,用5-HT2A受体激动剂(DOI)或5-HT1A受体拮抗剂[(-)-吲哚洛尔]治疗几乎完全消除了褪黑素诱导的体温过低。数据表明,褪黑素增强了下丘脑5-HT1A受体的激活,并导致体温过低效应,这种效应可被DOI预期的高温效应所拮抗。

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