A microdialysis study of nucleus accumbens core and shell dopamine during operant responding in the rat

被引:90
作者
Sokolowski, JD [1 ]
Conlan, AN [1 ]
Salamone, JD [1 ]
机构
[1] Univ Connecticut, Dept Psychol, Storrs, CT 06269 USA
基金
美国国家科学基金会;
关键词
reinforcement; motivation; motor; dialysis; release; lever pressing;
D O I
10.1016/S0306-4522(98)00066-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This investigation examined dopamine release and metabolism in nucleus accumbens core and shell during three operant tasks in the rat. Rats were trained to lever press on a fixed-ratio 5, variable-interval 30 s, or a tandem variable interval 30/fixed-ratio 5 schedules, these three schedules were chosen because they generate a wide range of response and reinforcement rates. After several weeks of training, dialysis probes were implanted into nucleus accumbens core or shell subregions. A single 30 min behavioural session was conducted during the dialysis test session. Rats lever pressing on each of the three operant schedules showed a significant increase in extracellular dopamine relative to the food-deprived control group during the behavioural session. In addition, increases in dopamine in nucleus accumbens shell were found to be significantly greater than in the core during the lever pressing period. Across all three schedules, extracellular dopamine in the nucleus accumbens was significantly correlated with the number of lever presses performed, but was not correlated with the number of food pellets delivered. Analysis of covariance, which used amount of food consumed as the covariate, showed an overall group difference, indicating that dopamine levels increased in lever pressing animals even if one corrected for the amount of food consumed. These results indicate that dopamine release was more responsive in the nucleus accumbens shell than in the core during operant responding, and that increases in extracellular dopamine in nucleus accumbens are related to response rate rather than reinforcement magnitude. (C) 1998 IBRO. Published by Elsevier Science Ltd.
引用
收藏
页码:1001 / 1009
页数:9
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