Nutt D J, Taylor S C, Little H J, Standing B L, Gale R G
University Department of Pharmacology, Oxford, UK.
Psychopharmacology (Berl). 1988;95(3):407-12. doi: 10.1007/BF00181957.
Mice were given flurazepam, 40 mg k-1, IP, once daily for 7 consecutive days. Twenty-four and forty-eight hours after the last injection measurements were made of the effects on convulsion threshold, body temperature and locomotor activity, of drugs acting on the GABA receptor complex. Significant decreases were seen in the hypothermic and hypomobility effects of progabide at 48 h, but no significant changes were seen in the effects of pentylenetetrazol or pentobarbitone. The actions of picrotoxin in all three types of test and the convulsant action of bicuculline (IP) were significantly decreased at 24 h but not at 48 h. The convulsive, but not the hypothermic, effects of picrotoxin were increased at the 48 h interval. These results may suggest that the chronic benzodiazepine treatment decreased some aspects of GABA receptor function at 48 h after the last dose; however, such an effect probably does not explain the previously reported increases in the effects of inverse agonists following chronic agonist treatment.
给小鼠腹腔注射氟西泮,剂量为40mg/kg,每日一次,连续7天。在最后一次注射后24小时和48小时,测量作用于GABA受体复合物的药物对惊厥阈值、体温和运动活性的影响。48小时时,普罗加比的降温及运动减少作用显著降低,但戊四氮或戊巴比妥的作用未见显著变化。24小时时,印防己毒素在所有三种测试类型中的作用以及荷包牡丹碱(腹腔注射)的惊厥作用显著降低,但48小时时未见此现象。48小时间隔时,印防己毒素的惊厥作用增强,但降温作用未增强。这些结果可能表明,末次给药后48小时,长期苯二氮䓬治疗降低了GABA受体功能的某些方面;然而,这种效应可能无法解释先前报道的长期激动剂治疗后反向激动剂作用增强的现象。