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

Functional pain syndromes diffuse hypersensitivity injury free red light-emitting diode widespread pain

Journal

The journal of pain
ISSN: 1528-8447
Titre abrégé: J Pain
Pays: United States
ID NLM: 100898657

Informations de publication

Date de publication:
11 2019
Historique:
received: 08 11 2018
revised: 23 02 2019
accepted: 15 04 2019
pubmed: 6 5 2019
medline: 15 9 2020
entrez: 6 5 2019
Statut: ppublish

Résumé

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 rostral 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.

Identifiants

pubmed: 31054915
pii: S1526-5900(18)30814-9
doi: 10.1016/j.jpain.2019.04.008
pmc: PMC6824986
mid: NIHMS1528412
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1293-1306

Subventions

Organisme : NINDS NIH HHS
ID : K08 NS104272
Pays : United States
Organisme : NCCIH NIH HHS
ID : R01 AT009716
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA042852
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS098772
Pays : United States

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2019 the American Pain Society. Published by Elsevier Inc. All rights reserved.

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Auteurs

Rajesh Khanna (R)

Department of Anesthesiology, University of Arizona, Tucson, Arizona; Department of Pharmacology, University of Arizona, Tucson, Arizona; Department of Graduate Interdisciplinary Program in Neuroscience College of Medicine, University of Arizona, Tucson, Arizona.

Amol Patwardhan (A)

Department of Anesthesiology, University of Arizona, Tucson, Arizona; Department of Pharmacology, University of Arizona, Tucson, Arizona.

Xiaofang Yang (X)

Department of Pharmacology, University of Arizona, Tucson, Arizona.

Wennan Li (W)

Department of Pharmacology, University of Arizona, Tucson, Arizona.

Song Cai (S)

Department of Pharmacology, University of Arizona, Tucson, Arizona.

Yingshi Ji (Y)

Department of Pharmacology, University of Arizona, Tucson, Arizona.

Lindsey A Chew (LA)

Department of Pharmacology, University of Arizona, Tucson, Arizona.

Angie Dorame (A)

Department of Pharmacology, University of Arizona, Tucson, Arizona.

Shreya S Bellampalli (SS)

Department of Pharmacology, University of Arizona, Tucson, Arizona.

Ryan W Schmoll (RW)

Department of Anesthesiology, University of Arizona, Tucson, Arizona.

Janalee Gordon (J)

Department of Anesthesiology, University of Arizona, Tucson, Arizona.

Aubin Moutal (A)

Department of Pharmacology, University of Arizona, Tucson, Arizona.

Todd W Vanderah (TW)

Department of Pharmacology, University of Arizona, Tucson, Arizona.

Frank Porreca (F)

Department of Anesthesiology, University of Arizona, Tucson, Arizona; Department of Pharmacology, University of Arizona, Tucson, Arizona.

Mohab M Ibrahim (MM)

Department of Anesthesiology, University of Arizona, Tucson, Arizona; Department of Pharmacology, University of Arizona, Tucson, Arizona. Electronic address: mibrahim@anesth.arizona.edu.

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Classifications MeSH