Literature DB >> 26852657

Quantification of pain in sickle mice using facial expressions and body measurements.

Aditya Mittal1, Mihir Gupta2, Yann Lamarre1, Balkrishna Jahagirdar1, Kalpna Gupta3.   

Abstract

Pain is a hallmark feature of sickle cell disease (SCD). Subjects typically quantify pain by themselves, which can be biased by other factors leading to overtreatment or under-treatment. Reliable and accurate quantification of pain, in real time, might enable to provide appropriate levels of analgesic treatment. The mouse grimace scale (MGS), a standardized behavioral coding system with high accuracy and reliability has been used to quantify varied types of pain. We hypothesized that addition of the objective parameters of body length and back curvature will strengthen the reproducibility of MGS. We examined MGS scores and body length and back curvature of transgenic BERK sickle and control mice following cold treatment or following treatment with analgesic cannabinoid CP55,940. We observed that sickle mice demonstrated decreased length and increased back curvature in response to cold. These observations correlate with changes in facial expression for the MGS score. CP55,940 treatment of sickle mice showed an increase in body length and a decrease in back curvature concordant with MGS scores indicative of an analgesic effect. Thus, body parameters combined with facial expressions may provide a quantifiable unbiased method for objective measure of pain in SCD.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cannabinoid; Hyperalgesia; Mouse grimace scale; Pain; Sickle cell disease

Mesh:

Substances:

Year:  2015        PMID: 26852657      PMCID: PMC4746724          DOI: 10.1016/j.bcmd.2015.12.006

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  32 in total

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3.  Transient receptor potential vanilloid 1 mediates pain in mice with severe sickle cell disease.

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6.  IMPROVE trial: a randomized controlled trial of patient-controlled analgesia for sickle cell painful episodes: rationale, design challenges, initial experience, and recommendations for future studies.

Authors:  Carlton D Dampier; Wally R Smith; Carrie G Wager; Hae-Young Kim; Margaret C Bell; Scott T Miller; Debra L Weiner; Caterina P Minniti; Lakshmanan Krishnamurti; Kenneth I Ataga; James R Eckman; Lewis L Hsu; Donna McClish; Sonja M McKinlay; Robert Molokie; Ifeyinwa Osunkwo; Kim Smith-Whitley; Marilyn J Telen
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1.  Influence of Rater Training on Inter- and Intrarater Reliability When Using the Rat Grimace Scale.

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6.  End points for sickle cell disease clinical trials: patient-reported outcomes, pain, and the brain.

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10.  CaMKIIα underlies spontaneous and evoked pain behaviors in Berkeley sickle cell transgenic mice.

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