Glue P, Bailey J, Wilson S, Hudson A, Nutt D J
Reckitt and Colman Psychopharmacology Unit, School of Medical Sciences, University Walk, Bristol, UK.
Life Sci. 1992;50(6):PL25-30. doi: 10.1016/0024-3205(92)90382-y.
To investigate preliminary reports that benzodiazepine-induced sedation may be reversed by thyrotropin-releasing hormone (TRH), we examined the effect of TRH or saline placebo on two variables which are sensitive to benzodiazepine agonists: changes in sedation and saccadic eye movements. Lorazepam 10 micrograms/kg i.v. increased self-ratings of sedation and reduced self-ratings of alertness and these changes were almost completely reversed by TRH. In contrast the slowing of saccadic eye movements by lorazepam was not reversed by TRH. The effects of TRH do not appear to be due to a direct antagonism at the benzodiazepine receptor, since flumazenil reverses changes in both variables. Moreover ligand binding studies reveal that TRH has very low affinity at this receptor. These clinical data provide the first demonstration that it is possible to distinguish between the effects of benzodiazepines on saccadic eye movements and psychological self-ratings.
为了研究关于促甲状腺激素释放激素(TRH)可能逆转苯二氮䓬类药物所致镇静作用的初步报告,我们检测了TRH或生理盐水安慰剂对两个对苯二氮䓬类激动剂敏感的变量的影响:镇静作用的变化和眼球跳动。静脉注射10微克/千克的劳拉西泮会增加自我评定的镇静作用,并降低自我评定的警觉性,而这些变化几乎被TRH完全逆转。相比之下,劳拉西泮所致的眼球跳动减慢并未被TRH逆转。TRH的作用似乎并非由于对苯二氮䓬受体的直接拮抗作用,因为氟马西尼可逆转这两个变量的变化。此外,配体结合研究表明TRH对该受体的亲和力非常低。这些临床数据首次证明,有可能区分苯二氮䓬类药物对眼球跳动和心理自我评定的影响。