Raghanti M A, Stimpson C D, Marcinkiewicz J L, Erwin J M, Hof P R, Sherwood C C
Department of Anthropology and School of Biomedical Sciences, Kent State University, Kent, OH 44242, USA.
Neuroscience. 2008 Jul 31;155(1):203-20. doi: 10.1016/j.neuroscience.2008.05.008. Epub 2008 May 20.
In this study, we assessed the possibility that humans differ from other primate species in the supply of dopamine to the frontal cortex. To this end, quantitative comparative analyses were performed among humans, chimpanzees, and macaques using immunohistochemical methods to visualize tyrosine hydroxylase-immunoreactive axons within the cerebral cortex. Axon densities and neuron densities were quantified using computer-assisted stereology. Prefrontal areas 9 and 32 were chosen for evaluation due to their roles in higher-order executive functions and theory of mind, respectively. Primary motor cortex (area 4) was also evaluated because it is not directly associated with cognition. We did not find an overt quantitative increase in cortical dopaminergic innervation in humans relative to the other primates examined. However, several differences in cortical dopaminergic innervation were observed among species which may have functional implications. Specifically, humans exhibited a sublaminar pattern of innervation in layer I of areas 9 and 32 that differed from that of macaques and chimpanzees. Analysis of axon length density to neuron density among species revealed that humans and chimpanzees together deviated from macaques in having increased dopaminergic afferents in layers III and V/VI of areas 9 and 32, but there were no phylogenetic differences in area 4. Finally, morphological specializations of axon coils that may be indicative of cortical plasticity events were observed in humans and chimpanzees, but not macaques. Our findings suggest significant modifications of dopamine's role in cortical organization occurred in the evolution of the apes, with further changes in the descent of humans.
在本研究中,我们评估了人类与其他灵长类物种在向额叶皮质供应多巴胺方面存在差异的可能性。为此,我们使用免疫组织化学方法对人类、黑猩猩和猕猴进行了定量比较分析,以可视化大脑皮质内酪氨酸羟化酶免疫反应性轴突。使用计算机辅助体视学对轴突密度和神经元密度进行了量化。由于前额叶区域9和32分别在高阶执行功能和心理理论中发挥作用,因此选择它们进行评估。初级运动皮质(区域4)也进行了评估,因为它与认知没有直接关联。我们没有发现相对于其他被检查的灵长类动物,人类皮质多巴胺能神经支配有明显的定量增加。然而,在不同物种之间观察到了皮质多巴胺能神经支配的一些差异,这些差异可能具有功能意义。具体而言,人类在区域9和32的第I层表现出一种与猕猴和黑猩猩不同的亚层神经支配模式。对不同物种轴突长度密度与神经元密度的分析表明,人类和黑猩猩在区域9和32的第III层和第V/VI层中多巴胺能传入增加,这与猕猴不同,但在区域4没有系统发育差异。最后,在人类和黑猩猩中观察到了可能指示皮质可塑性事件的轴突线圈形态特化,但在猕猴中未观察到。我们的研究结果表明,在猿类进化过程中,多巴胺在皮质组织中的作用发生了重大改变,在人类的演化过程中又有进一步变化。