M1 and M2 Muscarinic Acetylcholine Receptor Subtypes Mediate Ca2+ Channel Current Inhibition in Rat Sympathetic Stellate Ganglion Neurons

• Published in: Journal of neurophysiology Vol. 96; no. 5; p. 2479
• Main Authors: Yang, Qing, Sumner, Andrew D, Puhl, Henry L, Ruiz-Velasco, Victor
• Format: Journal Article
• Language: English
• Published: Am Phys Soc 01.11.2006
• DOI: 10.1152/jn.00093.2006
• ISSN: 0022-3077

1 Departments of Anesthesiology and 2 Medicine, Penn State College of Medicine, Hershey, Pennsylvania; and 3 Laboratory of Molecular Physiology, National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland Submitted 27 January 2006; accepted in final form 4 August 2006 Muscarinic acetylcholine receptors (mAChRs) are known to mediate the acetylcholine inhibition of Ca 2+ channels in central and peripheral neurons. Stellate ganglion (SG) neurons provide the main sympathetic input to the heart and contribute to the regulation of heart rate and myocardial contractility. Little information is available regarding mAChR regulation of Ca 2+ channels in SG neurons. The purpose of this study was to identify the mAChR subtypes that modulate Ca 2+ channel currents in rat SG neurons innervating heart muscle. Accordingly, the modulation of Ca 2+ channel currents by the muscarinic cholinergic agonist, oxotremorine-methiodide (Oxo-M), and mAChR blockers was examined. Oxo-M–mediated mAChR stimulation led to inhibition of Ca 2+ currents through voltage-dependent (VD) and voltage-independent (VI) pathways. Pre-exposure of SG neurons to the M 1 receptor blocker, M 1 -toxin, resulted in VD inhibition of Ca 2+ currents after Oxo-M application. On the other hand, VI modulation of Ca 2+ currents was observed after pretreatment of cells with methoctramine (M 2 mAChR blocker). The Oxo-M–mediated inhibition was nearly eliminated in the presence of both M 1 and M 2 mAChR blockers but was unaltered when SG neurons were exposed to the M 4 mAChR toxin, M 4 -toxin. Finally, the results from single-cell RT-PCR and immunofluorescence assays indicated that M 1 and M 2 receptors are expressed and located on the surface of SG neurons. Overall, the results indicate that SG neurons that innervate cardiac muscle express M 1 and M 2 mAChR, and activation of these receptors leads to inhibition of Ca 2+ channel currents through VI and VD pathways, respectively. Address for reprint requests and other correspondence: V. Ruiz-Velasco, Dept. of Anesthesiology, H187, Penn State College of Medicine, 500 University Dr., Hershey, PA 17033-0850 (E-mail: vruizvelasco{at}psu.edu )