Department of Psychology, University of California, Los Angeles, CA 90095-1563, USA.
Biol Psychiatry. 2013 Apr 15;73(8):756-62. doi: 10.1016/j.biopsych.2012.12.002. Epub 2013 Jan 16.
The compulsive and inflexible behaviors that are present in many psychiatric disorders, particularly behavioral addictions and obsessive-compulsive disorder, may be due to neurochemical dysfunction within the circuitry that enables goal-directed behaviors. Experimental removal of serotonin or dopamine within the orbitofrontal cortex or dorsal striatum, respectively, impairs flexible responding in a reversal learning test, suggesting that these neurochemical systems exert important modulatory influences on goal-directed behaviors. Nevertheless, the behavioral impairments present in psychiatric disorders are likely due to subtle neurochemical differences, and it remains unknown whether naturally occurring variation in neurochemical levels associate with individual differences in flexible, reward-directed behaviors.
The current study assessed the ability of 24 individual juvenile monkeys to acquire, retain, and reverse discrimination problems and examined whether monoamine levels in the orbitofrontal cortex, caudate nucleus, and putamen could explain variance in behavior.
The interaction between dopamine levels in the putamen and serotonin levels in the orbitofrontal cortex explained 61% of the variance in a measure of behavioral flexibility but not measures of associative learning or memory. The interaction mirrored that of a hyperbolic function, with reversal learning performance being poorest in either monkeys with relatively low levels of orbitofrontal serotonin and putamen dopamine or in monkeys with relatively high levels of orbitofrontal serotonin and putamen dopamine levels.
These results support the hypothesis that subcortical and cortical neuromodulatory systems interact to guide aspects of goal-directed behavior, providing insight into the neurochemical dysfunction that may underlie the inflexible and compulsive behaviors present in psychiatric disorders.
许多精神疾病中存在的强迫性和不灵活行为,特别是行为成瘾和强迫症,可能是由于使目标导向行为成为可能的神经回路中的神经化学功能障碍所致。分别在眶额皮层或背侧纹状体中实验性去除 5-羟色胺或多巴胺,会损害反转学习测试中的灵活反应,表明这些神经化学系统对目标导向行为施加了重要的调节影响。然而,精神疾病中存在的行为障碍可能是由于神经化学的细微差异所致,并且尚不清楚神经化学水平的自然变化是否与灵活的、奖励导向行为的个体差异相关。
本研究评估了 24 只幼年猴子获得、保留和反转辨别问题的能力,并检查了眶额皮层、尾状核和壳核中的单胺水平是否可以解释行为差异。
纹状体中的多巴胺水平与眶额皮层中的 5-羟色胺水平之间的相互作用解释了行为灵活性的 61%的方差,但不能解释联想学习或记忆的测量值。相互作用反映了双曲线函数的相互作用,在眶额皮质中相对较低的 5-羟色胺和纹状体多巴胺水平或眶额皮质中相对较高的 5-羟色胺和纹状体多巴胺水平的猴子中,反转学习表现最差。
这些结果支持了这样的假设,即皮质下和皮质神经调节系统相互作用以指导目标导向行为的各个方面,为可能导致精神疾病中出现的不灵活和强迫性行为的神经化学功能障碍提供了深入了解。