Ho I K
J Pharmacol Exp Ther. 1976 Jun;197(3):479-87.
Rapid tolerance development to pentobarbital by pentobarbital pellet implantation was evidenced by a decrease in sleeping time after challenge with different doses of sodium pentobarbital ranging from 37.5 to 100 mg/kg i.p. or a fixed dose of 75 mg/kg i.p. of the drug. The sleeping time produced by sodium pentobarbital decreased by 50% after 1 day. After 2 or 3 days of implantation, the sleeping time was generally further decreased to 15 to 20% of the placebo control group. Tolerance to pentobarbital was still evident 72 hours after pellet removal. The tolerance development to pentobarbital by pentobarbital pellet implantation also was demonstrated by other pentobarbital-induced responses such as hypothermia and lethality. In mice implanted with a 75-mg pentobarbital pellet for 3 days, the degree and duration of pentobarbital-induced hypothermia by intraperitoneal or intracerebral administration of the drug was attenuated. The chronic administration of pentobarbital by three days of pellet implantation reduced the effect of sodium pentobarbital on lethality as evidenced by an increase in the LD50 of sodium pentobarbital after intraperitoneal or intracerebral administration of the drug.
戊巴比妥颗粒植入导致对戊巴比妥快速产生耐受性,这表现为用37.5至100mg/kg腹腔注射不同剂量的戊巴比妥钠或固定剂量75mg/kg腹腔注射该药物进行激发后睡眠时间减少。戊巴比妥钠产生的睡眠时间在1天后减少了50%。植入2或3天后,睡眠时间通常进一步降至安慰剂对照组的15%至20%。取出颗粒72小时后,对戊巴比妥的耐受性仍然明显。戊巴比妥颗粒植入导致对戊巴比妥产生耐受性还表现为其他戊巴比妥诱导的反应,如体温过低和致死性。在植入75mg戊巴比妥颗粒3天的小鼠中,腹腔或脑内给药戊巴比妥诱导的体温过低的程度和持续时间减弱。通过颗粒植入3天进行戊巴比妥的慢性给药降低了戊巴比妥钠对致死性的影响,这表现为腹腔或脑内给药该药物后戊巴比妥钠的半数致死量增加。