McCormick D A, Wang Z, Huguenard J
Section of Neurobiology, Yale University School of Medicine, New Haven, Connecticut 06510.
Cereb Cortex. 1993 Sep-Oct;3(5):387-98. doi: 10.1093/cercor/3.5.387.
The pattern of activity and excitability of cortical neurons and neuronal circuits is dependent upon the interaction between glutamatergic and GABAergic fast-activating transmitter systems as well as the state of the more slowly acting transmitters such as ACh, norepinephrine, 5-HT, and histamine. Through the activation of GABAA receptors, GABAergic neurons regulate the amplitude and duration of EPSPs and, in so doing, control the level of functional activation of NMDA receptors. In contrast, activation of muscarinic, adrenergic, serotoninergic, histaminergic, and glutamate metabotropic receptors controls the excitability and pattern of action potential generation in identified pyramidal cells through increases or decreases in various K+ conductances. Activation of muscarinic, alpha 1-adrenergic, or glutamate metabotropic receptors on layer V burst-generating corticotectal or corticopontine neurons results in depolarization through a reduction in a K+ conductance and a switch in the firing mode from repetitive burst firing to single-spike activity. In contrast, activation of muscarinic, beta-adrenergic, H2-histaminergic, and serotoninergic receptors on regular-spiking layer II/III, V, and/or VI corticogeniculate pyramidal cells results in a decrease in spike frequency adaptation and increased responsiveness to depolarizing inputs through a reduction in a slow Ca(2+)-activated K+ current IAHP, and/or a voltage-dependent K+ current, IM. Through these, and other, mechanisms the spatial and temporal pattern of activity generated in cortical circuits is regulated by both intracortical and extracortical neurotransmitter systems.
皮质神经元和神经回路的活动模式与兴奋性取决于谷氨酸能和γ-氨基丁酸能快速激活递质系统之间的相互作用,以及作用较为缓慢的递质(如乙酰胆碱、去甲肾上腺素、5-羟色胺和组胺)的状态。通过激活GABAA受体,γ-氨基丁酸能神经元调节兴奋性突触后电位(EPSP)的幅度和持续时间,从而控制N-甲基-D-天冬氨酸受体(NMDA受体)的功能激活水平。相反,毒蕈碱能、肾上腺素能、5-羟色胺能、组胺能和谷氨酸代谢型受体的激活,通过增加或降低各种钾离子电导,控制特定锥体细胞中动作电位产生的兴奋性和模式。激活V层爆发性产生的皮质顶盖或皮质脑桥神经元上的毒蕈碱能、α1-肾上腺素能或谷氨酸代谢型受体,会通过降低钾离子电导导致去极化,并使放电模式从重复性爆发放电转变为单峰活动。相反,在规则放电的II/III层、V层和/或VI层皮质膝状体锥体细胞上激活毒蕈碱能、β-肾上腺素能、H2-组胺能和5-羟色胺能受体,会导致放电频率适应性降低,并通过降低缓慢的钙激活钾电流IAHP和/或电压依赖性钾电流IM,增加对去极化输入的反应性。通过这些及其他机制,皮质回路中产生的活动的空间和时间模式受到皮质内和皮质外神经递质系统的调节。