Matsuda T, Kanda T, Seong Y H, Baba A, Iwata H
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Osaka University, Japan.
Eur J Pharmacol. 1990 Jun 8;181(3):295-7. doi: 10.1016/0014-2999(90)90092-k.
The i.p. injection of 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) caused hypothermia and increased the concentrations of serum corticosterone and plasma ACTH in mice. The effects of 8-OH-DPAT at a dose of 2 mg/kg but not of 0.2 mg/kg on the hormone levels were attenuated by pretreatment with p-chlorophenylalanine (pCPA) which depleted brain 5-HT by about 70%; the hypothermic effect of 8-OH-DPAT was, however, not prevented. Similar results were obtained with another 5-HT1A agonist, 1-[3-(3,4-methylenedioxyphenoxy)propyl]-4-phenyl piperazine (BP-554).
腹腔注射8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)可导致小鼠体温过低,并增加其血清皮质酮和血浆促肾上腺皮质激素(ACTH)的浓度。剂量为2mg/kg而非0.2mg/kg的8-OH-DPAT对激素水平的影响可被对氯苯丙氨酸(pCPA)预处理减弱,pCPA可使脑内5-羟色胺(5-HT)耗竭约70%;然而,8-OH-DPAT的体温过低效应并未被阻止。使用另一种5-HT1A激动剂1-[3-(3,4-亚甲二氧基苯氧基)丙基]-4-苯基哌嗪(BP-554)也获得了类似结果。