Stanford S C, Taylor S C, Little H J
Department of Pharmacology, Middlesex Hospital Medical School, London, U.K.
Eur J Pharmacol. 1987 Jul 9;139(2):225-32. doi: 10.1016/0014-2999(87)90255-x.
The beta-carboline FG7142 is a partial inverse agonist at benzodiazepine receptors. We have shown previously that a single dose of this drug causes an upregulation of cortical beta-adrenoceptor numbers in mouse cerebral cortex. This rise was seen seven days, but not 15-30 min or 24 h after FG7142 administration. We now report that two weeks pretreatment with the tricyclic antidepressant desipramine prevented the beta-adrenoceptor upregulation after a single dose of FG7142, although desipramine alone did not alter beta-adrenoceptor number. We also studied the effects of desipramine pretreatment on other pharmacological effects of FG7142 to see which of these effects might be related to the beta-adrenoceptor changes. Desipramine pretreatment caused a small, but significant, decrease in the depression of locomotor activity, but no change in the hypothermic action of FG7142. The possibility that upregulation of beta-adrenoceptors by FG7142 may be related to the behavioural actions of this compound is discussed.
β-咔啉FG7142是苯二氮䓬受体的部分反向激动剂。我们之前已经表明,单次给药该药物会导致小鼠大脑皮层中皮质β-肾上腺素能受体数量上调。这种增加在FG7142给药后7天出现,但在给药后15 - 30分钟或24小时未出现。我们现在报告,用三环类抗抑郁药地昔帕明进行两周预处理可防止单次给药FG7142后β-肾上腺素能受体上调,尽管单独使用地昔帕明不会改变β-肾上腺素能受体数量。我们还研究了地昔帕明预处理对FG7142其他药理作用的影响,以确定这些作用中哪些可能与β-肾上腺素能受体变化有关。地昔帕明预处理导致运动活动抑制有小幅但显著的降低,但FG7142的体温过低作用没有变化。本文讨论了FG7142引起的β-肾上腺素能受体上调可能与其行为作用相关的可能性。