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The effect of robenacoxib on the concentration of C-reactive protein in synovial fluid from dogs with osteoarthritis

BACKGROUND: Robenacoxib is a novel and highly selective inhibitor of COX-2 in dogs and cats and because of its acidic nature is regarded as being tissue-selective. Thirty four dogs with stifle osteoarthritis secondary to failure of the cranial cruciate ligament were recruited into this study. Lamene...

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Autores principales: Bennett, David, Eckersall, Peter David, Waterston, Mary, Marchetti, Veronica, Rota, Alessandra, McCulloch, Eilidh, Sbrana, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3610148/
https://www.ncbi.nlm.nih.gov/pubmed/23452411
http://dx.doi.org/10.1186/1746-6148-9-42
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author Bennett, David
Eckersall, Peter David
Waterston, Mary
Marchetti, Veronica
Rota, Alessandra
McCulloch, Eilidh
Sbrana, Silvia
author_facet Bennett, David
Eckersall, Peter David
Waterston, Mary
Marchetti, Veronica
Rota, Alessandra
McCulloch, Eilidh
Sbrana, Silvia
author_sort Bennett, David
collection PubMed
description BACKGROUND: Robenacoxib is a novel and highly selective inhibitor of COX-2 in dogs and cats and because of its acidic nature is regarded as being tissue-selective. Thirty four dogs with stifle osteoarthritis secondary to failure of the cranial cruciate ligament were recruited into this study. Lameness, radiographic features, synovial cytology and C-reactive protein concentrations in serum and synovial fluid were assessed before and 28 days after commencing a course of Robenacoxib at a dose of 1 mg/kg SID. RESULTS: There was a significant reduction in the lameness score (P < 0.01) and an increase in the radiographic score (P < 0.05) between pre- and post-treatment assessments. There was no difference between pre- (median 1.49 mg/l; Q1-Q3 0.56-4.24 mg/L) and post – (1.10 mg/L; 0.31-1.78 mg/L) treatment serum C-reactive protein levels although synovial fluid levels were significantly reduced (pre- : 0.44 mg/L; 0.23-1.62 mg/L; post- : 0.17 mg/L; 0.05-0.49 mg/L) (P < 0.05). There was no correlation between C-reactive protein concentrations in serum and matched synovial fluid samples. CONCLUSIONS: Robenacoxib proved effective in reducing lameness in dogs with failure of the cranial cruciate ligament and osteoarthritis of the stifle joint. The drug also reduced levels of C-reactive protein in the synovial fluid taken from the affected stifle joint. Robenacoxib appears to reduce articular inflammation as assessed by C-reactive protein which supports the concept that Robenacoxib is a tissue-selective non-steroidal anti-inflammatory drug.
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spelling pubmed-36101482013-03-29 The effect of robenacoxib on the concentration of C-reactive protein in synovial fluid from dogs with osteoarthritis Bennett, David Eckersall, Peter David Waterston, Mary Marchetti, Veronica Rota, Alessandra McCulloch, Eilidh Sbrana, Silvia BMC Vet Res Research Article BACKGROUND: Robenacoxib is a novel and highly selective inhibitor of COX-2 in dogs and cats and because of its acidic nature is regarded as being tissue-selective. Thirty four dogs with stifle osteoarthritis secondary to failure of the cranial cruciate ligament were recruited into this study. Lameness, radiographic features, synovial cytology and C-reactive protein concentrations in serum and synovial fluid were assessed before and 28 days after commencing a course of Robenacoxib at a dose of 1 mg/kg SID. RESULTS: There was a significant reduction in the lameness score (P < 0.01) and an increase in the radiographic score (P < 0.05) between pre- and post-treatment assessments. There was no difference between pre- (median 1.49 mg/l; Q1-Q3 0.56-4.24 mg/L) and post – (1.10 mg/L; 0.31-1.78 mg/L) treatment serum C-reactive protein levels although synovial fluid levels were significantly reduced (pre- : 0.44 mg/L; 0.23-1.62 mg/L; post- : 0.17 mg/L; 0.05-0.49 mg/L) (P < 0.05). There was no correlation between C-reactive protein concentrations in serum and matched synovial fluid samples. CONCLUSIONS: Robenacoxib proved effective in reducing lameness in dogs with failure of the cranial cruciate ligament and osteoarthritis of the stifle joint. The drug also reduced levels of C-reactive protein in the synovial fluid taken from the affected stifle joint. Robenacoxib appears to reduce articular inflammation as assessed by C-reactive protein which supports the concept that Robenacoxib is a tissue-selective non-steroidal anti-inflammatory drug. BioMed Central 2013-03-01 /pmc/articles/PMC3610148/ /pubmed/23452411 http://dx.doi.org/10.1186/1746-6148-9-42 Text en Copyright ©2013 Bennett et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bennett, David
Eckersall, Peter David
Waterston, Mary
Marchetti, Veronica
Rota, Alessandra
McCulloch, Eilidh
Sbrana, Silvia
The effect of robenacoxib on the concentration of C-reactive protein in synovial fluid from dogs with osteoarthritis
title The effect of robenacoxib on the concentration of C-reactive protein in synovial fluid from dogs with osteoarthritis
title_full The effect of robenacoxib on the concentration of C-reactive protein in synovial fluid from dogs with osteoarthritis
title_fullStr The effect of robenacoxib on the concentration of C-reactive protein in synovial fluid from dogs with osteoarthritis
title_full_unstemmed The effect of robenacoxib on the concentration of C-reactive protein in synovial fluid from dogs with osteoarthritis
title_short The effect of robenacoxib on the concentration of C-reactive protein in synovial fluid from dogs with osteoarthritis
title_sort effect of robenacoxib on the concentration of c-reactive protein in synovial fluid from dogs with osteoarthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3610148/
https://www.ncbi.nlm.nih.gov/pubmed/23452411
http://dx.doi.org/10.1186/1746-6148-9-42
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