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J Neurophysiol 100: 1184-1201, 2008. First published May 28, 2008; doi:10.1152/jn.01344.2007
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Dorsal Root Ganglion Neurons Innervating Skeletal Muscle Respond to Physiological Combinations of Protons, ATP, and Lactate Mediated by ASIC, P2X, and TRPV1

Alan R. Light1,2, Ronald W. Hughen1, Jie Zhang3, Jon Rainier4, Zhuqing Liu4 and Jeewoo Lee5

1Departments of Anesthesiology, 2Neurobiology and Anatomy, 3Physiology, and 4Chemistry, University of Utah, Salt Lake City, Utah; and 5College of Pharmacy, Seoul National University, Seoul, Korea

Submitted 13 December 2007; accepted in final form 27 May 2008

The adequate stimuli and molecular receptors for muscle metaboreceptors and nociceptors are still under investigation. We used calcium imaging of cultured primary sensory dorsal root ganglion (DRG) neurons from C57Bl/6 mice to determine candidates for metabolites that could be the adequate stimuli and receptors that could detect these stimuli. Retrograde DiI labeling determined that some of these neurons innervated skeletal muscle. We found that combinations of protons, ATP, and lactate were much more effective than individually applied compounds for activating rapid calcium increases in muscle-innervating dorsal root ganglion neurons. Antagonists for P2X, ASIC, and TRPV1 receptors suggested that these three receptors act together to detect protons, ATP, and lactate when presented together in physiologically relevant concentrations. Two populations of muscle-innervating DRG neurons were found. One responded to low metabolite levels (likely nonnoxious) and used ASIC3, P2X5, and TRPV1 as molecular receptors to detect these metabolites. The other responded to high levels of metabolites (likely noxious) and used ASIC3, P2X4, and TRPV1 as their molecular receptors. We conclude that a combination of ASIC, P2X5 and/or P2X4, and TRPV1 are the molecular receptors used to detect metabolites by muscle-innervating sensory neurons. We further conclude that the adequate stimuli for muscle metaboreceptors and nociceptors are combinations of protons, ATP, and lactate.


Address for reprint requests and other correspondence: A. R. Light, Department of Anethesiology and Neurobiology and Anatomy, 3C444 SOM, University of Utah School of Medicine, 30N. 1900E., Salt Lake City, UT 84132-2304 (E-mail: alan.light{at}hsc.utah.edu)







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