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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Main Authors: T.A. Rodrigues, A.J.B. Sampaio Junior, I.D.P. Nunes, M.S.S. Cartágenes, J.B.S. Garcia
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2017000900602&lng=en&tlng=en
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spelling doaj-ff05fa2ed97845289200faa5ef33c3da2020-11-24T23:20:20ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research1414-431X50910.1590/1414-431x20176314S0100-879X2017000900602Effect of strontium ranelate on pain behavior in an experimental model of osteoarthritisT.A. RodriguesA.J.B. Sampaio JuniorI.D.P. NunesM.S.S. CartágenesJ.B.S. GarciaStrontium 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.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2017000900602&lng=en&tlng=enOsteoarthritisStrontium ranelatePainTreatmentProphylaxis
collection DOAJ
language English
format Article
sources DOAJ
author T.A. Rodrigues
A.J.B. Sampaio Junior
I.D.P. Nunes
M.S.S. Cartágenes
J.B.S. Garcia
spellingShingle T.A. Rodrigues
A.J.B. Sampaio Junior
I.D.P. Nunes
M.S.S. Cartágenes
J.B.S. Garcia
Effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis
Brazilian Journal of Medical and Biological Research
Osteoarthritis
Strontium ranelate
Pain
Treatment
Prophylaxis
author_facet T.A. Rodrigues
A.J.B. Sampaio Junior
I.D.P. Nunes
M.S.S. Cartágenes
J.B.S. Garcia
author_sort T.A. Rodrigues
title 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_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_sort effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis
publisher Associação Brasileira de Divulgação Científica
series Brazilian Journal of Medical and Biological Research
issn 1414-431X
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.
topic Osteoarthritis
Strontium ranelate
Pain
Treatment
Prophylaxis
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2017000900602&lng=en&tlng=en
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