Glick S D, Hinds P A
Eur J Pharmacol. 1985 Dec 3;118(3):239-44. doi: 10.1016/0014-2999(85)90134-7.
Morphine and d-amphetamine were tested for their effects on locomotor activity and for their propensities to be intravenously self-administered in rats that had been screened for their tendencies to rotate (turn in circles) spontaneously at night; noctural rotation was used as a behavioral index of asymmetry in the dopaminergic nigrostriatal system. Lateralized (rotating) rats were more sensitive to the locomotor stimulant effects of d-amphetamine than non-lateralized (non-rotating) rats. The stimulant effects of low doses of morphine were also greater in lateralized rats, whereas the depressant effects of high doses of morphine were greater in non-lateralized rats. Lateralized rats self-administered more d-amphetamine than non-lateralized rats whereas non-lateralized rats self-administered more morphine than lateralized rats. The data indicate that the degree of lateralization in some brain pathways is a source of interindividual variation in drug sensitivity--this may in part be responsible for the individual tendencies of humans to selectively abuse particular types of drugs.
对吗啡和右旋苯丙胺进行了测试,观察它们对大鼠运动活动的影响以及静脉自我给药的倾向。这些大鼠经过筛选,以确定其夜间自发旋转(转圈)的倾向;夜间旋转被用作多巴胺能黑质纹状体系统不对称性的行为指标。与非偏侧化(不旋转)的大鼠相比,偏侧化(旋转)的大鼠对右旋苯丙胺的运动兴奋作用更敏感。低剂量吗啡的兴奋作用在偏侧化大鼠中也更强,而高剂量吗啡的抑制作用在非偏侧化大鼠中更强。偏侧化大鼠比非偏侧化大鼠自我给药更多的右旋苯丙胺,而非偏侧化大鼠比偏侧化大鼠自我给药更多的吗啡。数据表明,某些脑通路的偏侧化程度是药物敏感性个体间差异的一个来源——这可能部分解释了人类个体选择性滥用特定类型药物的倾向。