Facilitation of Long-Term Potentiation by Muscarinic M1 Receptors Is Mediated by Inhibition of SK Channels

被引:154
作者
Buchanan, Katherine A. [1 ,2 ]
Petrovic, Milos M. [1 ]
Chamberlain, Sophie E. L. [1 ]
Marrion, Neil V. [1 ]
Mellor, Jack R. [1 ]
机构
[1] Univ Bristol, Med Res Council Ctr Synapt Plast, Sch Physiol & Pharmacol, Bristol BS8 1TD, Avon, England
[2] UCL, Dept Neurosci Physiol & Pharmacol, London WC1E 6BT, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会; 英国惠康基金;
关键词
CA2+-ACTIVATED K+ CHANNELS; PROTEIN-KINASE CK2; SYNAPTIC PLASTICITY; RAT HIPPOCAMPUS; ACETYLCHOLINE-RECEPTORS; CHOLINERGIC INHIBITION; PROACTIVE-INTERFERENCE; PYRAMIDAL CELLS; NMDA RECEPTORS; CA1;
D O I
10.1016/j.neuron.2010.11.018
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Muscarinic receptor activation facilitates the induction of synaptic plasticity and enhances cognitive function. However, the specific muscarinic receptor subtype involved and the critical intracellular signaling pathways engaged have remained controversial. Here, we show that the recently discovered highly selective allosteric M-1 receptor agonist 77-LH-28-1 facilitates long-term potentiation (LTP) induced by theta burst stimulation at Schaffer collateral synapses in the hippocampus. Similarly, release of acetylcholine by stimulation of cholinergic fibers facilitates LTP via activation of M-1 receptors. N-methyl-D-aspartate receptor (NMDAR) opening during theta burst stimulation was enhanced by M-1 receptor activation, indicating this is the mechanism for LIP facilitation. M-1 receptors were found to enhance NMDAR activation by inhibiting SK channels that otherwise act to hyperpolarize postsynaptic spines and inhibit NMDAR opening. Thus, we describe a mechanism where M-1 receptor activation inhibits SK channels, allowing enhanced NMDAR activity and leading to a facilitation of LIP induction in the hippocampus.
引用
收藏
页码:948 / 963
页数:16
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