Biphasic Cholinergic Modulation of Reverberatory Activity in Neuronal Networks

被引:2
作者
Li, Xiao-Wei [1 ]
Ren, Yi [1 ]
Shi, Dong-Qing [1 ]
Qi, Lei [1 ]
Xu, Fang [2 ]
Xiao, Yanyang [2 ]
Lau, Pak-Ming [1 ,2 ]
Bi, Guo-Qiang [1 ,2 ]
机构
[1] Univ Sci & Technol China, Sch Life Sci, Div Life Sci & Med, CAS Key Lab Brain Funct & Dis, Hefei 230027, Anhui, Peoples R China
[2] Chinese Acad Sci, Shenzhen Hong Kong Inst Brain Sci Shenzhen Fundame, Brain Cognit & Brain Dis Inst BCBDI, Shenzhen Inst Adv Technol, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
Acetylcholine; Neuronal network; Reverberation; Synaptic current; Excitability; TIMING-DEPENDENT PLASTICITY; THETA-OSCILLATIONS; SYNAPTIC-TRANSMISSION; BASAL FOREBRAIN; NERVOUS-SYSTEM; ACETYLCHOLINE; ACTIVATION; RECEPTORS; NEUROMODULATION; CORTEX;
D O I
10.1007/s12264-022-01012-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Acetylcholine (ACh) is an important neuromodulator in various cognitive functions. However, it is unclear how ACh influences neural circuit dynamics by altering cellular properties. Here, we investigated how ACh influences reverberatory activity in cultured neuronal networks. We found that ACh suppressed the occurrence of evoked reverberation at low to moderate doses, but to a much lesser extent at high doses. Moreover, high doses of ACh caused a longer duration of evoked reverberation, and a higher occurrence of spontaneous activity. With whole-cell recording from single neurons, we found that ACh inhibited excitatory postsynaptic currents (EPSCs) while elevating neuronal firing in a dose-dependent manner. Furthermore, all ACh-induced cellular and network changes were blocked by muscarinic, but not nicotinic receptor antagonists. With computational modeling, we found that simulated changes in EPSCs and the excitability of single cells mimicking the effects of ACh indeed modulated the evoked network reverberation similar to experimental observations. Thus, ACh modulates network dynamics in a biphasic fashion, probably by inhibiting excitatory synaptic transmission and facilitating neuronal excitability through muscarinic signaling pathways.
引用
收藏
页码:731 / 744
页数:14
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