Effect of Intramuscular Protons, Lactate, and ATP on Muscle Hyperalgesia in Rats
Chronic muscle pain is a significant health problem leading to disability[1]. Muscle fatigue can exacerbate muscle pain. Metabolites, including ATP, lactate, and protons, are released during fatiguing exercise and produce pain in humans. These substances directly activate purinergic (P2X) and acid s...
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Published in | PloS one Vol. 10; no. 9; p. e0138576 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
17.09.2015
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
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Summary: | Chronic muscle pain is a significant health problem leading to disability[1]. Muscle fatigue can exacerbate muscle pain. Metabolites, including ATP, lactate, and protons, are released during fatiguing exercise and produce pain in humans. These substances directly activate purinergic (P2X) and acid sensing ion channels (ASICs) on muscle nociceptors, and when combined, produce a greater increase in neuron firing than when given alone. Whether the enhanced effect of combining protons, lactate, and ATP is the sum of individual effects (additive) or more than the sum of individual effects (synergistic) is unknown. Using a rat model of muscle nociceptive behavior, we tested each of these compounds individually over a range of physiologic and supra-physiologic concentrations. Further, we combined all three compounds in a series of dilutions and tested their effect on muscle nociceptive behavior. We also tested a non-hydrolyzable form of ATP (α,β-meATP) alone and in combination with lactate and acidic pH. Surprisingly, we found no dose-dependent effect on muscle nociceptive behavior for protons, lactate, or ATP when given alone. We similarly found no effect after application of each two-metabolite combination. Only pH 4 saline and α,β-meATP produced hyperalgesia when given alone. When all 3 substances were combined, however, ATP (2.4μm), lactate (10mM), and acidic pH (pH 6.0) produced an enhanced effect greater than the sum of the effects of the individual components, i.e. synergism. α,β me ATP (3nmol), on the other hand, showed no enhanced effects when combined with lactate (10mM) or acidic pH (pH 6.0), i.e. additive. These data suggest that combining fatigue metabolites in muscle produces a synergistic effect on muscle nociception. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Conceived and designed the experiments: KS NG PW. Performed the experiments: NG. Analyzed the data: NG KS. Wrote the paper: KS NG PW. Competing Interests: Dr. Phillip E. Whitley is employed by CFD Research Corporation and was the Principal Investigator on a Small Business Innovative Research project, contract number: N68335-13-C-0062 with the US Navy, to develop a computational model to predict back pain. This research was not in direct support of a product or commercial development of CFD Research Corporation but was an effort supporting a US Government research need. This research was not funded with any CFD Research Corporation corporate funds or any commercial funding from any source. Dr. Phillip E. Whitley was 51% employee whose time was supported during this research effort as an hourly employee that receives no benefits and has no stocks or ownership or holdings in the company in any way. The work performed by the University of Iowa under this effort provided valuable information to assist in computational model validation which will be freely available to all by open source publication. Given the intended use of this information, Dr. Whitley’s was an active collaborator in design and analysis of data. Further the collaboration in study design insured that the experimental conditions and collected data were usable for subsequent model validation. There are no patents, products in development, or marketed products to declare. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors. |
ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0138576 |