Fletcher P J
Section of Biopsychology, Clarke Institute of Psychiatry, Toronto, Ontario, Canada.
Psychopharmacology (Berl). 1996 Jul;126(1):62-9. doi: 10.1007/BF02246412.
Injection of d-amphetamine into the nucleus accumbens potentiates responding for stimuli paired with a primary reward. A previous study showed that this potentiating effect of d-amphetamine on responding for conditioned reward (CR) was attenuated by peripherally injected d-fenfluramine, a 5-hydroxytryptamine (5-HT) releaser and re-uptake inhibitor. The present experiments further examined the effects of manipulating 5-HT function within the nucleus accumbens on responding for CR, and on the potentiation of CR responding following intra-accumbens injection of d-amphetamine. Water deprived rats were trained to associate a compound stimulus with water delivery during a conditioning phase. During a test phase water was not delivered, but the compound stimulus was delivered according to a random ratio 2 schedule following a response on one of two levers. Rats responded at a higher rate on the lever delivering this CR. d-Amphetamine (10 micrograms) injected into the nucleus accumbens enhanced responding on the CR lever. Co-injections of 5-HT (5 and 10 micrograms) into the nucleus accumbens abolished the response-potentiating effect of d-amphetamine but were without effect on the base-line level of responding for CR. This reduction by 5-HT of the response potentiating effect of d-amphetamine was prevented by prior treatment with the 5-HT receptor antagonist metergoline (1 mg/kg). Responding for water was not altered by 5-HT and so the effects of 5-HT on responding for CR cannot be due to a change in the motivation to seek the primary reward. Thus, elevating 5-HT activity within the nucleus accumbens antagonises the effect of d-amphetamine on responding for CR within the nucleus accumbens. These results suggest that 5-HT within the nucleus accumbens may play an important role in mediating incentive motivation by modulating dopaminergic neurotransmission.
向伏隔核注射右旋苯丙胺可增强对与初级奖励配对的刺激的反应。先前的一项研究表明,外周注射右旋芬氟拉明(一种5-羟色胺(5-HT)释放剂和再摄取抑制剂)可减弱右旋苯丙胺对条件性奖励(CR)反应的这种增强作用。本实验进一步研究了在伏隔核内操纵5-HT功能对CR反应以及伏隔核内注射右旋苯丙胺后CR反应增强的影响。对水剥夺的大鼠在条件化阶段进行训练,使其将复合刺激与水的递送联系起来。在测试阶段不提供水,但在两个杠杆之一上做出反应后,根据随机比率2的时间表递送复合刺激。大鼠在递送这种CR的杠杆上以更高的速率做出反应。向伏隔核注射右旋苯丙胺(10微克)可增强在CR杠杆上的反应。向伏隔核共注射5-HT(5微克和10微克)可消除右旋苯丙胺的反应增强作用,但对CR反应的基线水平没有影响。5-HT对右旋苯丙胺反应增强作用的这种降低可通过预先用5-HT受体拮抗剂麦角林(1毫克/千克)治疗来预防。5-HT对水的反应没有改变,因此5-HT对CR反应的影响不可能是由于寻求初级奖励的动机发生了变化。因此,提高伏隔核内的5-HT活性可拮抗右旋苯丙胺对伏隔核内CR反应的影响。这些结果表明,伏隔核内的5-HT可能通过调节多巴胺能神经传递在介导激励动机中发挥重要作用。