PT - JOURNAL ARTICLE AU - Hong-Mei Zhang AU - De-Pei Li AU - Shao-Rui Chen AU - Hui-Lin Pan TI - M<sub>2</sub>, M<sub>3</sub>, and M<sub>4</sub> Receptor Subtypes Contribute to Muscarinic Potentiation of GABAergic Inputs to Spinal Dorsal Horn Neurons AID - 10.1124/jpet.104.079939 DP - 2005 May 01 TA - Journal of Pharmacology and Experimental Therapeutics PG - 697--704 VI - 313 IP - 2 4099 - http://jpet.aspetjournals.org/content/313/2/697.short 4100 - http://jpet.aspetjournals.org/content/313/2/697.full SO - J Pharmacol Exp Ther2005 May 01; 313 AB - The spinal cholinergic system and muscarinic receptors are important for regulation of nociception. Activation of spinal muscarinic receptors produces analgesia and inhibits dorsal horn neurons through potentiation of GABAergic inputs. To determine the role of receptor subtypes in the muscarinic agonist-induced synaptic GABA release, spontaneous inhibitory postsynaptic currents (sIPSCs) were recorded in lamina II neurons using whole-cell voltage-clamp recordings in rat spinal cord slices. The muscarinic receptor agonist oxotremorine-M dose-dependently (1–10 μM) increased GABAergic sIPSCs but not miniature IPSCs. The potentiating effect of oxotremorine-M on sIPSCs was completely blocked by atropine. In rats pretreated with intrathecal pertussis toxin to inactive inhibitory G i/o proteins, 3 μM oxotremorine-M had no significant effect on sIPSCs in 31 of 55 (56%) neurons tested. In the remaining 24 (44%) neurons in pertussis toxin-treated rats, oxotremorine-M caused a small increase in sIPSCs, and this effect was completely abolished by subsequent application of 25 nM 4-diphenylacetoxy-N-methylpiperidine methiodide (4-DAMP), a relatively selective M3 subtype antagonist. Furthermore, himbacine (1 μM), a relatively specific antagonist for M2 and M4 subtypes, produced a large reduction in the stimulatory effect of oxotremorine-M on sIPSCs, and the remaining effect was abolished by 4-DAMP. Additionally, the M4 receptor antagonist MT-3 toxin (100 nM) significantly attenuated the effect of oxotremorine-M on sIPSCs. Collectively, these data suggest that M2 and M4 receptor subtypes play a predominant role in muscarinic potentiation of synaptic GABA release in the spinal cord. The M3 subtype also contributes to increased GABAergic tone in spinal dorsal horn by muscarinic agonists. The American Society for Pharmacology and Experimental Therapeutics