Kantak K M, Miczek K A
Department of Psychology, Tufts University, Medford, MA 02155.
Psychopharmacology (Berl). 1988;96(4):468-76. doi: 10.1007/BF02180026.
Drugs that predominantly influence catecholamines were used in order to simultaneously determine their ability to alter salient signs of social, motor and autonomic activity during morphine withdrawal, and to compare the sensitivity of each of these signs to these drugs. Cocaine, d-amphetamine, apomorphine and L-dopa increased attack and threat, but did not induce defensive behavior in morphine-withdrawn resident mice who were more responsive to the aggression-enhancing effects of these drugs than placebo control mice. Concurrently measured withdrawal jumping was not affected by these drugs, and the sensitivity to the hypothermic effects of these drugs was reduced. In contrast, clonidine decreased attack and threat behaviors, and morphine-withdrawn mice were more sensitive to this inhibitory influence. But like the stimulant drugs, clonidine did not affect withdrawal jumping, and the hypothermic action of clonidine was attenuated in morphine-withdrawn mice. These findings show that in mice, opiate withdrawal leads to altered attack and threat that is further amplified by catecholaminergic drugs. The present pattern of results indicates differential drug effects on social, motor and autonomic functions when the behaviors are measured 48 h following withdrawal.
为了同时确定主要影响儿茶酚胺的药物改变吗啡戒断期间社会、运动和自主活动显著体征的能力,并比较这些体征对这些药物的敏感性,使用了这些药物。可卡因、右旋苯丙胺、阿扑吗啡和左旋多巴增加了攻击和威胁行为,但在吗啡戒断的定居小鼠中未诱发防御行为,这些小鼠比安慰剂对照小鼠对这些药物的攻击增强作用更敏感。同时测量的戒断跳跃不受这些药物影响,且对这些药物低温效应的敏感性降低。相比之下,可乐定减少了攻击和威胁行为,吗啡戒断小鼠对这种抑制作用更敏感。但与兴奋剂药物一样,可乐定不影响戒断跳跃,且可乐定在吗啡戒断小鼠中的低温作用减弱。这些发现表明,在小鼠中,阿片类药物戒断会导致攻击和威胁行为改变,而儿茶酚胺能药物会进一步放大这种改变。目前的结果模式表明,在戒断48小时后测量行为时,药物对社会、运动和自主功能有不同影响。