Aranko K
Acta Pharmacol Toxicol (Copenh). 1985 May;56(5):373-81. doi: 10.1111/j.1600-0773.1985.tb01306.x.
Development of cross-tolerance between lorazepam and four other benzodiazepines (BZ) was studied in two trials by measuring objective psychomotor performance and by subjective assessments. In trial I, nitrazepam 10 mg (NZ), temazepam 20 mg (TZ) or placebo were administered to 14 healthy students for 10 consecutive nights. After each pretreatment, psychomotor impairment by the challenge dose of lorazepam 3 mg (LZ) was measured. In trial II, responses to LZ after pretreatment with diazepam 5 mg (DZ) (8 subjects) or alprazolam 0.25 mg (AZ) (10 subjects), both t.i.d., were compared to LZ responses measured after one-month wash-out period. In trial I no cross-tolerance between BZs was found in objective tests, and LZ induced exophoria was even increased. However, the subjects rated LZ to cause less drowsiness after pretreatment with NZ in a situation where the manifestation of cross-tolerance was facilitated by ingestion of caffeine. In trial II a clear but task-dependent development of tolerance to the challenge dose of LZ was documented. One-week pretreatment with DZ reduced subjects responses to LZ. The total serum BZ activity bioassayed by radioreceptor method after intake of LZ was significantly (P less than 0.05) higher after pretreatment with DZ than in the end of wash-out period. Thus a functional cross-tolerance was documented on complex tasks after the subjects have been continuously working under DZ burden.
通过测量客观精神运动表现和主观评估,在两项试验中研究了劳拉西泮与其他四种苯二氮䓬类药物(BZ)之间交叉耐受性的发展。在试验I中,对14名健康学生连续10个晚上给予10毫克硝西泮(NZ)、20毫克替马西泮(TZ)或安慰剂。每次预处理后,测量3毫克劳拉西泮(LZ)激发剂量引起的精神运动损害。在试验II中,将5毫克地西泮(DZ)(8名受试者)或0.25毫克阿普唑仑(AZ)(10名受试者)每日三次预处理后对LZ的反应,与经过一个月洗脱期后测量的LZ反应进行比较。在试验I中,在客观测试中未发现BZ之间的交叉耐受性,LZ诱发的外隐斜甚至增加。然而,在摄入咖啡因促进交叉耐受性表现的情况下,受试者认为在NZ预处理后LZ引起的嗜睡较少。在试验II中,记录到对LZ激发剂量的耐受性有明显但依赖任务的发展。DZ一周的预处理降低了受试者对LZ的反应。摄入LZ后通过放射受体法测定的总血清BZ活性,在DZ预处理后显著(P小于0.05)高于洗脱期末。因此,在受试者持续处于DZ负荷下工作后,在复杂任务上记录到了功能性交叉耐受性。