Department of Psychiatry and Behavioral Sciences and National Primate Research Center, University of Washington, Seattle, Washington.
Department of Psychiatry, UT Southwestern Medical Center, Dallas, Texas.
J Comp Neurol. 2021 Nov;529(16):3564-3592. doi: 10.1002/cne.25188. Epub 2021 Jul 26.
The objective of the study was to identify brain structures that mediate reward as evidenced by positive reinforcing effects of stimuli on behavior. Testing by intracerebral self-stimulation enabled monkeys to inform whether activation of ~2900 sites in 74 structures of 4 sensorimotor pathways and 4 modulatory loop pathways was positive, negative or neutral. Stimulation was rewarding at 30% of sites, negative at 17%, neutral at 52%. Virtually all (99%) structures yielded some positive or negative sites, suggesting a ubiquitous distribution of pathways transmitting valence information. Mapping of sites to structures with dense versus sparse dopaminergic (DA) or noradrenergic (NA) innervation showed that stimulation of DA-pathways was rewarding or neutral. Stimulation of NA-pathways was not rewarding. Stimulation of association areas was generally rewarding; stimulation of purely sensory or motor structures was generally negative. Reward related more to structures' sensorimotor function than to density of DA-innervation. Stimulation of basal ganglia loop pathways was rewarding except in lateral globus pallidus, an inhibitory structure in the negative feedback loop; stimulation of the cerebellar loop was rewarding in anterior vermis and the spinocerebellar pathway; and stimulation of the hippocampal CA1 loop was rewarding. While most positive sites were in the DA reward system, numerous sites in sparsely DA-innervated posterior cingulate and parietal cortices may represent a separate reward system. DA-density represents concentrations of plastic synapses that mediate acquisition of new synaptic connections. DA-sparse areas may represent innate, genetically programmed reward-associated pathways. Implications of findings in regard to response habituation and addiction are discussed.
这项研究的目的是确定大脑结构作为中介,介导奖赏,因为刺激对行为具有积极的强化作用。通过脑内自我刺激,猴子可以告知 4 个感觉运动通路和 4 个调制环路中的 74 个结构中的 2900 个左右的位点的激活是阳性、阴性还是中性的。刺激在 30%的位点是奖赏性的,在 17%的位点是负性的,在 52%的位点是中性的。实际上(99%)所有结构都产生了一些阳性或阴性的位点,这表明传递效价信息的通路广泛分布。将位点映射到具有密集或稀疏多巴胺(DA)或去甲肾上腺素(NA)支配的结构,发现 DA 通路的刺激是奖赏性或中性的。NA 通路的刺激没有奖赏性。联合区的刺激通常是奖赏性的;而纯粹的感觉或运动结构的刺激通常是负性的。奖赏与结构的感觉运动功能有关,而与 DA 支配的密度无关。基底神经节环路的刺激是奖赏性的,除了外侧苍白球,这是负反馈环中的抑制性结构;小脑环路的刺激在前蚓部和脊髓小脑通路上是奖赏性的;而海马 CA1 环路的刺激是奖赏性的。虽然大多数阳性位点都在 DA 奖赏系统中,但在后扣带回和顶叶皮质中,DA 支配稀疏的许多位点可能代表了一个独立的奖赏系统。DA 密度代表了介导新突触连接获得的可塑突触的浓度。DA 稀疏区可能代表先天的、遗传编程的与奖赏相关的通路。讨论了这些发现对反应习惯化和成瘾的影响。