Shuster L, Yu G, Bates A
Psychopharmacology (Berl). 1977 Apr 29;52(2):185-90. doi: 10.1007/BF00439108.
Repeated administration of cocaine to B6AF1/J mice increased their running response to 20 mg/kg cocaine as much as four-fold over the response to the first injection. After four daily injections, the extent of the increase was proportional to the dose of cocaine that was used for pretreatment. Sensitization persisted for as long as 2 months after the last injection of cocaine. Cocaine-pretreated mice did not show an increased running response to either morphine or d-amphetamine. The response to cocaine was increased two-fold by treatment with morphine and three-fold by pretreatment with d-amphetamine. Pretreatment with either imipramine or reserpine did not produce sensitization to cocaine. There was no correlation between cocaine sensitization and whole-brain catecholamine levels. There were marked differences in both the running response to cocaine and the extent of cocaine sensitization betwee the parental strains, C57B1/6J and A/J. Experiments with recombinant-inbred lines, derived from C57B1/6By and BALB/cBy mice, suggest that the initial response to cocaine and the development of sensitization are controlled by different genetic determinants.
对B6AF1/J小鼠重复给予可卡因,可使其对20mg/kg可卡因的奔跑反应比首次注射时增加多达四倍。在每日注射四次后,增加的程度与用于预处理的可卡因剂量成正比。在最后一次注射可卡因后,敏化作用持续长达2个月。经可卡因预处理的小鼠对吗啡或右旋苯丙胺均未表现出增加的奔跑反应。用吗啡治疗可使对可卡因的反应增加两倍,用右旋苯丙胺预处理可使其增加三倍。用丙咪嗪或利血平预处理均未产生对可卡因的敏化作用。可卡因敏化与全脑儿茶酚胺水平之间无相关性。亲本品系C57B1/6J和A/J在对可卡因的奔跑反应及可卡因敏化程度上均存在显著差异。对源自C57B1/6By和BALB/cBy小鼠的重组近交系进行的实验表明,对可卡因的初始反应和敏化作用的发展受不同的遗传决定因素控制。