Collagen‐induced arthritis as an animal model of rheumatoid cachexia

Abstract Background Rheumatoid arthritis is characterized by chronic polyarticular synovitis and presents systemic changes that impact quality of life, such as impaired muscle function, seen in up to 66% of the patients. This can progress to severely debilitating state known as rheumatoid cachexia—w...

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Main Authors: Paulo V.G. Alabarse, Priscila S. Lora, Jordana M.S. Silva, Rafaela C.E. Santo, Eduarda C. Freitas, Mayara S. deOliveira, Andrelise S. Almeida, Mônica Immig, Vivian O.N. Teixeira, Lidiane I. Filippin, Ricardo M. Xavier
Format: Article
Language:English
Published: Wiley 2018-06-01
Series:Journal of Cachexia, Sarcopenia and Muscle
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Online Access:https://doi.org/10.1002/jcsm.12280
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spelling doaj-744441f74aef4eb0abab6b5f0e02c4962020-11-24T23:07:57ZengWileyJournal of Cachexia, Sarcopenia and Muscle2190-59912190-60092018-06-019360361210.1002/jcsm.12280Collagen‐induced arthritis as an animal model of rheumatoid cachexiaPaulo V.G. Alabarse0Priscila S. Lora1Jordana M.S. Silva2Rafaela C.E. Santo3Eduarda C. Freitas4Mayara S. deOliveira5Andrelise S. Almeida6Mônica Immig7Vivian O.N. Teixeira8Lidiane I. Filippin9Ricardo M. Xavier10Laboratório de Doenças Autoimunes Hospital de Clínicas de Porto Alegre Porto Alegre BrazilLaboratório de Doenças Autoimunes Hospital de Clínicas de Porto Alegre Porto Alegre BrazilLaboratório de Doenças Autoimunes Hospital de Clínicas de Porto Alegre Porto Alegre BrazilLaboratório de Doenças Autoimunes Hospital de Clínicas de Porto Alegre Porto Alegre BrazilLaboratório de Doenças Autoimunes Hospital de Clínicas de Porto Alegre Porto Alegre BrazilLaboratório de Doenças Autoimunes Hospital de Clínicas de Porto Alegre Porto Alegre BrazilLaboratório de Doenças Autoimunes Hospital de Clínicas de Porto Alegre Porto Alegre BrazilLaboratório de Doenças Autoimunes Hospital de Clínicas de Porto Alegre Porto Alegre BrazilLaboratório de Doenças Autoimunes Hospital de Clínicas de Porto Alegre Porto Alegre BrazilLaboratório de Doenças Autoimunes Hospital de Clínicas de Porto Alegre Porto Alegre BrazilLaboratório de Doenças Autoimunes Hospital de Clínicas de Porto Alegre Porto Alegre BrazilAbstract Background Rheumatoid arthritis is characterized by chronic polyarticular synovitis and presents systemic changes that impact quality of life, such as impaired muscle function, seen in up to 66% of the patients. This can progress to severely debilitating state known as rheumatoid cachexia—without loss of fat mass and body weight—for which there is little consensus in terms of diagnosis or treatment. This study aims to evaluate whether the collagen‐induced arthritis (CIA) animal model also develops clinical and functional features characteristic of rheumatoid cachexia. Methods Male DBA1/J mice were randomly divided into 2 groups: healthy animals (CO, n = 11) and CIA animals (n = 13). The clinical score and edema size, animal weight and food intake, free exploratory locomotion, grip strength, and endurance exercise performance were tested 0, 18, 35, 45, 55, and 65 days after disease induction. After euthanasia, several organs, visceral and brown fat, and muscles were dissected and weighed. Muscles were used to assess myofiber diameter. Ankle joint was used to assess arthritis severity by histological score. Statistical analysis were performed using one‐way and two‐way analyses of variance followed by Tukey's and Bonferroni's test or t‐test of Pearson and statistical difference were assumed for a P value under 0.05. Results The CIA had significantly higher arthritis scores and larger hind paw edema volumes than CO. The CIA had decreased endurance exercise performance total time (fatigue; 23, 22, 24, and 21% at 35, 45, 55, and 65 days, respectively), grip strength (27, 55, 63, 60, and 66% at 25, 35, 45, 55, and 65 days, respectively), free locomotion (43, 57, 59, and 66% at 35, 45, 55, and 65 days, respectively), and tibialis anterior and gastrocnemius muscle weight (25 and 24%, respectively) compared with CO. Sarcoplasmic ratios were also reduced in CIA (TA: 23 and GA: 22% less sarcoplasmic ratio), confirming the atrophy of skeletal muscle mass in these animals than in CO. Myofiber diameter was also reduced 45% in TA and 41% in GA in CIA when compared with the CO. Visceral and brown fat were lighter in CIA (54 and 39%, respectively) than CO group. Conclusions The CIA model is a valid experimental model for rheumatoid cachexia given that the clinical changes observed were similar to those described in patients with rheumatoid arthritis.https://doi.org/10.1002/jcsm.12280Collagen‐induced arthritisMuscle lossCachexiaRheumatoid arthritisMuscle wasting
collection DOAJ
language English
format Article
sources DOAJ
author Paulo V.G. Alabarse
Priscila S. Lora
Jordana M.S. Silva
Rafaela C.E. Santo
Eduarda C. Freitas
Mayara S. deOliveira
Andrelise S. Almeida
Mônica Immig
Vivian O.N. Teixeira
Lidiane I. Filippin
Ricardo M. Xavier
spellingShingle Paulo V.G. Alabarse
Priscila S. Lora
Jordana M.S. Silva
Rafaela C.E. Santo
Eduarda C. Freitas
Mayara S. deOliveira
Andrelise S. Almeida
Mônica Immig
Vivian O.N. Teixeira
Lidiane I. Filippin
Ricardo M. Xavier
Collagen‐induced arthritis as an animal model of rheumatoid cachexia
Journal of Cachexia, Sarcopenia and Muscle
Collagen‐induced arthritis
Muscle loss
Cachexia
Rheumatoid arthritis
Muscle wasting
author_facet Paulo V.G. Alabarse
Priscila S. Lora
Jordana M.S. Silva
Rafaela C.E. Santo
Eduarda C. Freitas
Mayara S. deOliveira
Andrelise S. Almeida
Mônica Immig
Vivian O.N. Teixeira
Lidiane I. Filippin
Ricardo M. Xavier
author_sort Paulo V.G. Alabarse
title Collagen‐induced arthritis as an animal model of rheumatoid cachexia
title_short Collagen‐induced arthritis as an animal model of rheumatoid cachexia
title_full Collagen‐induced arthritis as an animal model of rheumatoid cachexia
title_fullStr Collagen‐induced arthritis as an animal model of rheumatoid cachexia
title_full_unstemmed Collagen‐induced arthritis as an animal model of rheumatoid cachexia
title_sort collagen‐induced arthritis as an animal model of rheumatoid cachexia
publisher Wiley
series Journal of Cachexia, Sarcopenia and Muscle
issn 2190-5991
2190-6009
publishDate 2018-06-01
description Abstract Background Rheumatoid arthritis is characterized by chronic polyarticular synovitis and presents systemic changes that impact quality of life, such as impaired muscle function, seen in up to 66% of the patients. This can progress to severely debilitating state known as rheumatoid cachexia—without loss of fat mass and body weight—for which there is little consensus in terms of diagnosis or treatment. This study aims to evaluate whether the collagen‐induced arthritis (CIA) animal model also develops clinical and functional features characteristic of rheumatoid cachexia. Methods Male DBA1/J mice were randomly divided into 2 groups: healthy animals (CO, n = 11) and CIA animals (n = 13). The clinical score and edema size, animal weight and food intake, free exploratory locomotion, grip strength, and endurance exercise performance were tested 0, 18, 35, 45, 55, and 65 days after disease induction. After euthanasia, several organs, visceral and brown fat, and muscles were dissected and weighed. Muscles were used to assess myofiber diameter. Ankle joint was used to assess arthritis severity by histological score. Statistical analysis were performed using one‐way and two‐way analyses of variance followed by Tukey's and Bonferroni's test or t‐test of Pearson and statistical difference were assumed for a P value under 0.05. Results The CIA had significantly higher arthritis scores and larger hind paw edema volumes than CO. The CIA had decreased endurance exercise performance total time (fatigue; 23, 22, 24, and 21% at 35, 45, 55, and 65 days, respectively), grip strength (27, 55, 63, 60, and 66% at 25, 35, 45, 55, and 65 days, respectively), free locomotion (43, 57, 59, and 66% at 35, 45, 55, and 65 days, respectively), and tibialis anterior and gastrocnemius muscle weight (25 and 24%, respectively) compared with CO. Sarcoplasmic ratios were also reduced in CIA (TA: 23 and GA: 22% less sarcoplasmic ratio), confirming the atrophy of skeletal muscle mass in these animals than in CO. Myofiber diameter was also reduced 45% in TA and 41% in GA in CIA when compared with the CO. Visceral and brown fat were lighter in CIA (54 and 39%, respectively) than CO group. Conclusions The CIA model is a valid experimental model for rheumatoid cachexia given that the clinical changes observed were similar to those described in patients with rheumatoid arthritis.
topic Collagen‐induced arthritis
Muscle loss
Cachexia
Rheumatoid arthritis
Muscle wasting
url https://doi.org/10.1002/jcsm.12280
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