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    Development and Characterization of An Injury-free Model of Functional Pain in Rats by Exposure to Red Light

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    Final Accepted Manuscript
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    Author
    Khanna, Rajesh
    Patwardhan, Amol
    Yang, Xiaofang
    Li, Wennan
    Cai, Song
    Ji, Yingshi
    Chew, Lindsey A
    Dorame, Angie
    Bellampalli, Shreya S
    Schmoll, Ryan W
    Gordon, Janalee
    Moutal, Aubin
    Vanderah, Todd W
    Porreca, Frank
    Ibrahim, Mohab M
    Show allShow less
    Affiliation
    Univ Arizona, Dept Anesthesiol
    Univ Arizona, Dept Pharmacol
    Univ Arizona, Coll Med, Dept Grad Interdisciplinary Program Neurosci
    Issue Date
    2019-11-01
    Keywords
    Functional pain syndromes
    diffuse hypersensitivity
    injury free
    red light-emitting diode
    widespread pain
    
    Metadata
    Show full item record
    Publisher
    CHURCHILL LIVINGSTONE
    Citation
    Khanna, R., Patwardhan, A., Yang, X., Li, W., Cai, S., Ji, Y., ... & Gordon, J. (2019). Development and Characterization of An Injury-free Model of Functional Pain in Rats by Exposure to Red Light. The Journal of Pain.
    Journal
    JOURNAL OF PAIN
    Rights
    © 2019 by the American Pain Society.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    We report the development and characterization of a novel, injury-free rat model in which nociceptive sensitization after red light is observed in multiple body areas reminiscent of widespread pain in functional pain syndromes. Rats were exposed to red light-emitting diodes (RLED) (LEDs, 660 nm) at an intensity of 50 Lux for 8 hours daily for 5 days resulting in time- and dose-dependent thermal hyperalgesia and mechanical allodynia in both male and female rats. Females showed an earlier onset of mechanical allodynia than males. The pronociceptive effects of RLED were mediated through the visual system. RLED-induced thermal hyperalgesia and mechanical allodynia were reversed with medications commonly used for widespread pain, including gabapentin, tricyclic antidepressants, serotonin/norepinephrine reuptake inhibitors, and nonsteroidal anti-inflammatory drugs. Acetaminophen failed to reverse the RLED induced hypersensitivity. The hyperalgesic effects of RLED were blocked when bicuculline, a gamma-aminobutyric acid-A receptor antagonist, was administered into the rostra! ventromedial medulla, suggesting a role for increased descending facilitation in the pain pathway. Key experiments were subjected to a replication study with randomization, investigator blinding, inclusion of all data, and high levels of statistical rigor. RLED-induced thermal hyperalgesia and mechanical allodynia without injury offers a novel injury-free rodent model useful for the study of functional pain syndromes with widespread pain. RLED exposure also emphasizes the different biological effects of different colors of light exposure. Perspective: This study demonstrates the effect of light exposure on nociceptive thresholds. These biological effects of red LED add evidence to the emerging understanding of the biological effects of light of different colors in animals and humans. Understanding the underlying biology of red light-induced widespread pain may offer insights into functional pain states. (C) 2019 by the American Pain Society
    Note
    12 month embargo; published online: 2 May 2019
    ISSN
    1528-8447
    PubMed ID
    31054915
    DOI
    10.1016/j.jpain.2019.04.008
    Version
    Final accepted manuscript
    Sponsors
    National Center for Complementary and Alternative Health [R01AT009716]; National Institute for Neurological Disorders and StrokeUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of Neurological Disorders & Stroke (NINDS) [1R01N5098772]; NINDSUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of Neurological Disorders & Stroke (NINDS); Children's Tumor Foundation; University of Arizona
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.jpain.2019.04.008
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