Hutson P H, Donohoe T P, Curzon G
Department of Neurochemistry, Institute of Neurology, London, U.K.
Eur J Pharmacol. 1987 Nov 10;143(2):221-8. doi: 10.1016/0014-2999(87)90536-x.
The putative 5-HT1A agonist 1-[2-(4-aminophenyl)ethyl]-4-(3-trifluoromethylphenyl)piperazine (LY165163, PAPP) (1, 2, 4, 10 mg/kg s.c.) caused a significant and dose-dependent hypothermia in rats, 30 and 60 min after injection. The decreases of temperature were less marked than that caused by 8-OH-DPAT 1 mg/kg s.c.). Depletion of brain serotonin (5-HT) by 91% following pretreatment with p-chlorophenylalanine (pCPA) (150 mg/kg i.p. on three successive days) significantly enhanced the hypothermic effects of both 8-OH-DPAT (0.25 mg/kg s.c.) and LY165163 (4 mg/kg s.c.). LY165163-induced hypothermia was also somewhat enhanced following depletion of hypothalamic 5-HT by 76% after infusion of 5,7-dihydroxytryptamine (5,7-DHT) (150 micrograms) into the third ventricle. Results indicate that the hypothermia induced by the putative 5-HT1A agonists LY165163 and 8-OH-DPAT in the rat is not dependent on presynaptic 5-HT stores and is therefore probably mediated by postsynaptic 5-HT receptors.
假定的5-羟色胺1A(5-HT1A)激动剂1-[2-(4-氨基苯基)乙基]-4-(3-三氟甲基苯基)哌嗪(LY165163,PAPP)(1、2、4、10毫克/千克,皮下注射)在注射后30和60分钟,使大鼠体温显著下降,且呈剂量依赖性。体温下降程度不如皮下注射1毫克/千克的8-羟基二丙胺基四氢萘(8-OH-DPAT)明显。连续三天腹腔注射对氯苯丙氨酸(pCPA)(150毫克/千克)使脑内5-羟色胺(5-HT)耗竭91%后,显著增强了8-OH-DPAT(0.25毫克/千克,皮下注射)和LY165163(4毫克/千克,皮下注射)的降温作用。向第三脑室注入5,7-二羟基色胺(5,7-DHT)(150微克)使下丘脑5-HT耗竭76%后,LY165163诱导的体温过低也有所增强。结果表明,假定的5-HT1A激动剂LY165163和8-OH-DPAT在大鼠中诱导的体温过低不依赖于突触前5-HT储备,因此可能是由突触后5-HT受体介导的。