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Effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis

Strontium ranelate (SrRan) is a drug usually prescribed to treat osteoporosis, with proven effects of decreasing the risk of fractures and an indication of reducing the progression of osteoarthritis (OA). This study aimed to investigate the effects of SrRan as either a prophylactic or a treatment dr...

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Autores principales: Rodrigues, T.A., Sampaio, A.J.B., Nunes, I.D.P., Cartágenes, M.S.S., Garcia, J.B.S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572847/
https://www.ncbi.nlm.nih.gov/pubmed/28793056
http://dx.doi.org/10.1590/1414-431X20176314
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author Rodrigues, T.A.
Sampaio, A.J.B.
Nunes, I.D.P.
Cartágenes, M.S.S.
Garcia, J.B.S.
author_facet Rodrigues, T.A.
Sampaio, A.J.B.
Nunes, I.D.P.
Cartágenes, M.S.S.
Garcia, J.B.S.
author_sort Rodrigues, T.A.
collection PubMed
description Strontium ranelate (SrRan) is a drug usually prescribed to treat osteoporosis, with proven effects of decreasing the risk of fractures and an indication of reducing the progression of osteoarthritis (OA). This study aimed to investigate the effects of SrRan as either a prophylactic or a treatment drug, using an OA rat model to assess pain behavior. A monoiodoacetate (MIA)-induced knee joint OA model in Wistar rats was used. Thirty Wistar rats (both sexes, 60 days old) were distributed in five groups of 6 rats each: the control group, that received no intervention; a prophylactic group, that received oral administration of 25 mg·kg(-1)·day(-1) of SrRan for 28 days before induction of OA; a group treated with 25 mg·kg(-1)·day(-1) of SrRan for 28 days after OA induction; a group treated with 50 mg·kg(-1)·day(-1) during 28 days after OA induction; and a group that received oral saline for 28 days after induction. The assessment of pain behavior was performed considering articular incapacitation (weight-bearing test), mechanical hyperalgesia (Randall Selitto test) and motor activity (rotarod test), on days 0, 7, 14, 21, and 28. This experiment did not yield a significant difference when comparing the group that received SrRan prophylactically with the groups treated with 25 or 50 mg·kg(-1)·day(-1) and the group that received oral saline. Thus, SrRan did not provide analgesia in either treated rats or as a prophylactic drug with the tested doses. Higher doses should be tested further to achieve possible significant results.
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spelling pubmed-55728472017-08-31 Effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis Rodrigues, T.A. Sampaio, A.J.B. Nunes, I.D.P. Cartágenes, M.S.S. Garcia, J.B.S. Braz J Med Biol Res Research Articles Strontium ranelate (SrRan) is a drug usually prescribed to treat osteoporosis, with proven effects of decreasing the risk of fractures and an indication of reducing the progression of osteoarthritis (OA). This study aimed to investigate the effects of SrRan as either a prophylactic or a treatment drug, using an OA rat model to assess pain behavior. A monoiodoacetate (MIA)-induced knee joint OA model in Wistar rats was used. Thirty Wistar rats (both sexes, 60 days old) were distributed in five groups of 6 rats each: the control group, that received no intervention; a prophylactic group, that received oral administration of 25 mg·kg(-1)·day(-1) of SrRan for 28 days before induction of OA; a group treated with 25 mg·kg(-1)·day(-1) of SrRan for 28 days after OA induction; a group treated with 50 mg·kg(-1)·day(-1) during 28 days after OA induction; and a group that received oral saline for 28 days after induction. The assessment of pain behavior was performed considering articular incapacitation (weight-bearing test), mechanical hyperalgesia (Randall Selitto test) and motor activity (rotarod test), on days 0, 7, 14, 21, and 28. This experiment did not yield a significant difference when comparing the group that received SrRan prophylactically with the groups treated with 25 or 50 mg·kg(-1)·day(-1) and the group that received oral saline. Thus, SrRan did not provide analgesia in either treated rats or as a prophylactic drug with the tested doses. Higher doses should be tested further to achieve possible significant results. Associação Brasileira de Divulgação Científica 2017-08-07 /pmc/articles/PMC5572847/ /pubmed/28793056 http://dx.doi.org/10.1590/1414-431X20176314 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Rodrigues, T.A.
Sampaio, A.J.B.
Nunes, I.D.P.
Cartágenes, M.S.S.
Garcia, J.B.S.
Effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis
title Effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis
title_full Effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis
title_fullStr Effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis
title_full_unstemmed Effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis
title_short Effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis
title_sort effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572847/
https://www.ncbi.nlm.nih.gov/pubmed/28793056
http://dx.doi.org/10.1590/1414-431X20176314
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