Department of Biology, University of Texas at San Antonio, San Antonio, TX 78249, USA.
Neuroscience. 2011 Dec 15;198:54-68. doi: 10.1016/j.neuroscience.2011.06.049. Epub 2011 Jun 22.
Neurons in the subthalamic nucleus occupy a pivotal position in the circuitry of the basal ganglia. They receive direct excitatory input from the cerebral cortex and the intralaminar nuclei of the thalamus, and directly excite the inhibitory basal ganglia output neurons in the internal segment of the globus pallidus and the substantia nigra. They are also engaged in a reciprocal synaptic arrangement with inhibitory neurons in the external segment of the globus pallidus. Although once viewed as a simple relay of extrinsic input to the basal ganglia, physiological studies of subthalamic neurons have revealed that activity in these neurons does not directly reflect their pattern of extrinsic excitation. Subthalamic neurons are autonomously active at rates comparable to those observed in vivo, and they generate complex patterns of intrinsic activity arising from the interactions between voltage sensitive ion channels on the somatodendritic and axonal membranes. Extrinsic synaptic excitation does not create the firing pattern of the subthalamic neuron, but rather controls the timing of action potentials generated intrinsically. The dopaminergic innervation of the subthalamic nucleus, although moderate, can directly influence firing patterns by acting both on synaptic transmission and voltage-sensitive ion channels responsible for intrinsic properties. Furthermore, chronic dopamine depletion in Parkinson's disease may modify both synaptic transmission and integration in the subthalamic nucleus, in addition to its effects on other regions of the basal ganglia.
底丘脑核中的神经元在基底神经节的回路中占据着关键的位置。它们接收来自大脑皮层和丘脑的核间区的直接兴奋性输入,并直接兴奋苍白球内节和黑质中的抑制性基底神经节输出神经元。它们还与苍白球外节中的抑制性神经元形成交互性突触排列。尽管曾经被视为将外在输入简单传递到基底神经节的中继站,但对底丘脑神经元的生理学研究表明,这些神经元的活动并不能直接反映它们外在兴奋的模式。底丘脑神经元以与体内观察到的相似的速率自主活跃,它们产生复杂的内在活动模式,源自于躯体树突和轴突膜上电压敏感离子通道之间的相互作用。外在的突触兴奋不会产生底丘脑神经元的放电模式,而是控制内在产生的动作电位的时间。底丘脑核的多巴胺能神经支配虽然适度,但可以通过作用于负责内在特性的突触传递和电压敏感离子通道,直接影响放电模式。此外,帕金森病中的慢性多巴胺耗竭除了对基底神经节的其他区域产生影响外,还可能改变底丘脑核中的突触传递和整合。