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dc.contributor.authorKhanna, Rajesh
dc.contributor.authorPatwardhan, Amol
dc.contributor.authorYang, Xiaofang
dc.contributor.authorLi, Wennan
dc.contributor.authorCai, Song
dc.contributor.authorJi, Yingshi
dc.contributor.authorChew, Lindsey A
dc.contributor.authorDorame, Angie
dc.contributor.authorBellampalli, Shreya S
dc.contributor.authorSchmoll, Ryan W
dc.contributor.authorGordon, Janalee
dc.contributor.authorMoutal, Aubin
dc.contributor.authorVanderah, Todd W
dc.contributor.authorPorreca, Frank
dc.contributor.authorIbrahim, Mohab M
dc.date.accessioned2019-12-17T17:23:41Z
dc.date.available2019-12-17T17:23:41Z
dc.date.issued2019-11-01
dc.identifier.citationKhanna, 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.en_US
dc.identifier.issn1528-8447
dc.identifier.pmid31054915
dc.identifier.doi10.1016/j.jpain.2019.04.008
dc.identifier.urihttp://hdl.handle.net/10150/636390
dc.description.abstractWe 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 Societyen_US
dc.description.sponsorshipNational 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 Arizonaen_US
dc.language.isoenen_US
dc.publisherCHURCHILL LIVINGSTONEen_US
dc.rights© 2019 by the American Pain Society.en_US
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectFunctional pain syndromesen_US
dc.subjectdiffuse hypersensitivityen_US
dc.subjectinjury freeen_US
dc.subjectred light-emitting diodeen_US
dc.subjectwidespread painen_US
dc.titleDevelopment and Characterization of An Injury-free Model of Functional Pain in Rats by Exposure to Red Lighten_US
dc.typeArticleen_US
dc.contributor.departmentUniv Arizona, Dept Anesthesiolen_US
dc.contributor.departmentUniv Arizona, Dept Pharmacolen_US
dc.contributor.departmentUniv Arizona, Coll Med, Dept Grad Interdisciplinary Program Neuroscien_US
dc.identifier.journalJOURNAL OF PAINen_US
dc.description.note12 month embargo; published online: 2 May 2019en_US
dc.description.collectioninformationThis 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.en_US
dc.eprint.versionFinal accepted manuscripten_US
dc.source.journaltitleThe journal of pain : official journal of the American Pain Society


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