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Effects of stanozolol on normal and IL-1[beta]-stimulated equine chondrocytes in vitro

Background Intra-articular administration of stanozolol has shown promising results by improving the clinical management of lameness associated with naturally-occurring osteoarthritis (OA) in horses, and by decreasing osteophyte formation and subchondral bone reaction in sheep following surgically i...

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Published in:BMC veterinary research 2018-03, Vol.14 (1)
Main Authors: Castro Ma, Peffers, Mandy J, Lee, Katie, Rubio-Ma
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description Background Intra-articular administration of stanozolol has shown promising results by improving the clinical management of lameness associated with naturally-occurring osteoarthritis (OA) in horses, and by decreasing osteophyte formation and subchondral bone reaction in sheep following surgically induced OA. However, there is limited evidence on the anti-inflammatory and modulatory properties of stanozolol on articular tissues. The objective of the current study was to evaluate the effects of stanozolol on chondrocyte viability and gene expression in normal equine chondrocytes and an inflammatory in vitro system of OA (interleukin-1[beta] (IL-1[beta]) treated chondrocytes). Results Chondrocytes from normal metacarpophalangeal joints of skeletally mature horses were exposed to four treatment groups: (1) media only (2) media+IL-1[beta] (3) media+IL-1[beta] + stanozolol (4) media+stanozolol. Following exposure, chondrocyte viability and the expression of catabolic, anabolic and structural genes were determined. General linear models with Dunnet's comparisons with Bonferroni's adjustment were performed. Cell viability was similar in all groups. Stanozolol treatment reduced gene expression of MMP-13, MMP-1, IL-6 and COX-2 in both normal and IL-1[beta] treated chondrocytes. Stanozolol treatment reduced ADAMTS4 gene expression in normal chondrocytes. Stanozolol reduced the expression of COL2A1. Conclusions The current study demonstrates stanozolol has chondroprotective effects through downregulation of genes for pro-inflammatory/catabolic cytokines and enzymes associated with OA. However, there is no evidence of increased cartilage stimulation through upregulation of the anabolic and structural genes tested. Keywords: Osteoarthritis, Stanozolol, Chondrocyte, Equine, Gene expression, In vitro
doi_str_mv 10.1186/s12917-018-1426-z
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However, there is limited evidence on the anti-inflammatory and modulatory properties of stanozolol on articular tissues. The objective of the current study was to evaluate the effects of stanozolol on chondrocyte viability and gene expression in normal equine chondrocytes and an inflammatory in vitro system of OA (interleukin-1[beta] (IL-1[beta]) treated chondrocytes). Results Chondrocytes from normal metacarpophalangeal joints of skeletally mature horses were exposed to four treatment groups: (1) media only (2) media+IL-1[beta] (3) media+IL-1[beta] + stanozolol (4) media+stanozolol. Following exposure, chondrocyte viability and the expression of catabolic, anabolic and structural genes were determined. General linear models with Dunnet's comparisons with Bonferroni's adjustment were performed. Cell viability was similar in all groups. Stanozolol treatment reduced gene expression of MMP-13, MMP-1, IL-6 and COX-2 in both normal and IL-1[beta] treated chondrocytes. Stanozolol treatment reduced ADAMTS4 gene expression in normal chondrocytes. Stanozolol reduced the expression of COL2A1. Conclusions The current study demonstrates stanozolol has chondroprotective effects through downregulation of genes for pro-inflammatory/catabolic cytokines and enzymes associated with OA. However, there is no evidence of increased cartilage stimulation through upregulation of the anabolic and structural genes tested. Keywords: Osteoarthritis, Stanozolol, Chondrocyte, Equine, Gene expression, In vitro</description><identifier>ISSN: 1746-6148</identifier><identifier>EISSN: 1746-6148</identifier><identifier>DOI: 10.1186/s12917-018-1426-z</identifier><language>eng</language><publisher>BioMed Central Ltd</publisher><subject>Analysis ; Cartilage cells ; Dosage and administration ; Drug therapy ; Gene expression ; Genetic aspects ; Interleukin-1 ; Osteoarthritis ; Stanozolol</subject><ispartof>BMC veterinary research, 2018-03, Vol.14 (1)</ispartof><rights>COPYRIGHT 2018 BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids></links><search><creatorcontrib>Castro Ma</creatorcontrib><creatorcontrib>Peffers, Mandy J</creatorcontrib><creatorcontrib>Lee, Katie</creatorcontrib><creatorcontrib>Rubio-Ma</creatorcontrib><title>Effects of stanozolol on normal and IL-1[beta]-stimulated equine chondrocytes in vitro</title><title>BMC veterinary research</title><description>Background Intra-articular administration of stanozolol has shown promising results by improving the clinical management of lameness associated with naturally-occurring osteoarthritis (OA) in horses, and by decreasing osteophyte formation and subchondral bone reaction in sheep following surgically induced OA. However, there is limited evidence on the anti-inflammatory and modulatory properties of stanozolol on articular tissues. The objective of the current study was to evaluate the effects of stanozolol on chondrocyte viability and gene expression in normal equine chondrocytes and an inflammatory in vitro system of OA (interleukin-1[beta] (IL-1[beta]) treated chondrocytes). Results Chondrocytes from normal metacarpophalangeal joints of skeletally mature horses were exposed to four treatment groups: (1) media only (2) media+IL-1[beta] (3) media+IL-1[beta] + stanozolol (4) media+stanozolol. Following exposure, chondrocyte viability and the expression of catabolic, anabolic and structural genes were determined. General linear models with Dunnet's comparisons with Bonferroni's adjustment were performed. Cell viability was similar in all groups. Stanozolol treatment reduced gene expression of MMP-13, MMP-1, IL-6 and COX-2 in both normal and IL-1[beta] treated chondrocytes. Stanozolol treatment reduced ADAMTS4 gene expression in normal chondrocytes. Stanozolol reduced the expression of COL2A1. Conclusions The current study demonstrates stanozolol has chondroprotective effects through downregulation of genes for pro-inflammatory/catabolic cytokines and enzymes associated with OA. However, there is no evidence of increased cartilage stimulation through upregulation of the anabolic and structural genes tested. Keywords: Osteoarthritis, Stanozolol, Chondrocyte, Equine, Gene expression, In vitro</description><subject>Analysis</subject><subject>Cartilage cells</subject><subject>Dosage and administration</subject><subject>Drug therapy</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Interleukin-1</subject><subject>Osteoarthritis</subject><subject>Stanozolol</subject><issn>1746-6148</issn><issn>1746-6148</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptT8FKAzEUDKJgrX6At4Dn1LxuNtk9llK1sOCleBEpafJSI9kEN6lgv94FPfQgc5hhmBkYQm6BzwAaeZ9h3oJiHBoGYi7Z8YxMQAnJJIjm_ERfkqucPzgXolVyQl5WzqEpmSZHc9ExHVNIgaZIYxp6HaiOlq47Bq87LPqN5eL7Q9AFLcXPg49IzXuKdkjmu2CmPtIvX4Z0TS6cDhlv_nhKNg-rzfKJdc-P6-WiY3upWiYsYq34zvBG2XZ8IMFUWjk-yso5Z6WQFSAojUpgNa-t4dpZYXgrLNSmmpK739m9Drj10aUyaNP7bLaLWkiopeTtmJr9kxphsfcmRXR-9E8KP6dmYz4</recordid><startdate>20180320</startdate><enddate>20180320</enddate><creator>Castro Ma</creator><creator>Peffers, Mandy J</creator><creator>Lee, Katie</creator><creator>Rubio-Ma</creator><general>BioMed Central Ltd</general><scope/></search><sort><creationdate>20180320</creationdate><title>Effects of stanozolol on normal and IL-1[beta]-stimulated equine chondrocytes in vitro</title><author>Castro Ma ; Peffers, Mandy J ; Lee, Katie ; Rubio-Ma</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g679-4dee570bc087d912961c3a7f01293fffd64631e17ae74e325dc0afd4c094d15c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Analysis</topic><topic>Cartilage cells</topic><topic>Dosage and administration</topic><topic>Drug therapy</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Interleukin-1</topic><topic>Osteoarthritis</topic><topic>Stanozolol</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Castro Ma</creatorcontrib><creatorcontrib>Peffers, Mandy J</creatorcontrib><creatorcontrib>Lee, Katie</creatorcontrib><creatorcontrib>Rubio-Ma</creatorcontrib><jtitle>BMC veterinary research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Castro Ma</au><au>Peffers, Mandy J</au><au>Lee, Katie</au><au>Rubio-Ma</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of stanozolol on normal and IL-1[beta]-stimulated equine chondrocytes in vitro</atitle><jtitle>BMC veterinary research</jtitle><date>2018-03-20</date><risdate>2018</risdate><volume>14</volume><issue>1</issue><issn>1746-6148</issn><eissn>1746-6148</eissn><abstract>Background Intra-articular administration of stanozolol has shown promising results by improving the clinical management of lameness associated with naturally-occurring osteoarthritis (OA) in horses, and by decreasing osteophyte formation and subchondral bone reaction in sheep following surgically induced OA. However, there is limited evidence on the anti-inflammatory and modulatory properties of stanozolol on articular tissues. The objective of the current study was to evaluate the effects of stanozolol on chondrocyte viability and gene expression in normal equine chondrocytes and an inflammatory in vitro system of OA (interleukin-1[beta] (IL-1[beta]) treated chondrocytes). Results Chondrocytes from normal metacarpophalangeal joints of skeletally mature horses were exposed to four treatment groups: (1) media only (2) media+IL-1[beta] (3) media+IL-1[beta] + stanozolol (4) media+stanozolol. Following exposure, chondrocyte viability and the expression of catabolic, anabolic and structural genes were determined. General linear models with Dunnet's comparisons with Bonferroni's adjustment were performed. Cell viability was similar in all groups. Stanozolol treatment reduced gene expression of MMP-13, MMP-1, IL-6 and COX-2 in both normal and IL-1[beta] treated chondrocytes. Stanozolol treatment reduced ADAMTS4 gene expression in normal chondrocytes. Stanozolol reduced the expression of COL2A1. Conclusions The current study demonstrates stanozolol has chondroprotective effects through downregulation of genes for pro-inflammatory/catabolic cytokines and enzymes associated with OA. However, there is no evidence of increased cartilage stimulation through upregulation of the anabolic and structural genes tested. Keywords: Osteoarthritis, Stanozolol, Chondrocyte, Equine, Gene expression, In vitro</abstract><pub>BioMed Central Ltd</pub><doi>10.1186/s12917-018-1426-z</doi></addata></record>
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subjects Analysis
Cartilage cells
Dosage and administration
Drug therapy
Gene expression
Genetic aspects
Interleukin-1
Osteoarthritis
Stanozolol
title Effects of stanozolol on normal and IL-1[beta]-stimulated equine chondrocytes in vitro
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