Cartilage oligomeric matrix protein (COMP) is modified by intra-articular liposomal clodronate in an experimental model of arthritis

High-dose liposomal bisphosphonates exert apoptotic effects. This work studies the chondroprotective and anti-inflammatory properties of intra-articularly administered low-dose, non-cytotoxic liposomal clodronate. Antigen induced arthritis in rabbits was treated with intra-articular injections of li...

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Veröffentlicht in:Clinical and experimental rheumatology 2006-11, Vol.24 (6), p.622-628
Hauptverfasser: GOMEZ-BARRENA, E, LINDROOS, L, CEPORNS, A, LOPEZ-FRANCO, M, SANCHEZ-PERNAUTE, O, MONKKONEN, J, SALO, J, HERRERO-BEAUMONT, G, KONTTINEN, Y
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container_issue 6
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container_title Clinical and experimental rheumatology
container_volume 24
creator GOMEZ-BARRENA, E
LINDROOS, L
CEPORNS, A
LOPEZ-FRANCO, M
SANCHEZ-PERNAUTE, O
MONKKONEN, J
SALO, J
HERRERO-BEAUMONT, G
KONTTINEN, Y
description High-dose liposomal bisphosphonates exert apoptotic effects. This work studies the chondroprotective and anti-inflammatory properties of intra-articularly administered low-dose, non-cytotoxic liposomal clodronate. Antigen induced arthritis in rabbits was treated with intra-articular injections of liposomal clodronate. Drug effects on cartilage oligomeric matrix protein COMP was assessed using immunohistochemistry and morphometry of synovial membrane and hyaline articular cartilage. COMP remained close to normal in liposomal clodronate treated superficial articular cartilage compared to a significant loss of COMP in arthritis controls treated with empty liposomes. The middle and deep layers of the hyaline articular cartilage were characterized by highly increased COMP expression in liposomal clodronate treated AIA joints compared to controls. In contrast to cartilage, synovial COMP expression was slightly decreased as a result of liposomal clodronate treatment. Low-dose, non-cytotoxic liposomal clodronate exerts a dichotomous effect on synovial membrane and articular cartilage COMP in the AIA model. COMP is a useful inflammation marker in the synovial tissue, but it also contributes to the structural integrity of the hyaline articular cartilage forming bridges between type II and IX collagens. Enhancement of COMP in clodronate treated AIA cartilage suggests a chondroprotective and anti-inflammatory effect in the inflammatorily damaged and mechanically strained cartilage.
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This work studies the chondroprotective and anti-inflammatory properties of intra-articularly administered low-dose, non-cytotoxic liposomal clodronate. Antigen induced arthritis in rabbits was treated with intra-articular injections of liposomal clodronate. Drug effects on cartilage oligomeric matrix protein COMP was assessed using immunohistochemistry and morphometry of synovial membrane and hyaline articular cartilage. COMP remained close to normal in liposomal clodronate treated superficial articular cartilage compared to a significant loss of COMP in arthritis controls treated with empty liposomes. The middle and deep layers of the hyaline articular cartilage were characterized by highly increased COMP expression in liposomal clodronate treated AIA joints compared to controls. In contrast to cartilage, synovial COMP expression was slightly decreased as a result of liposomal clodronate treatment. Low-dose, non-cytotoxic liposomal clodronate exerts a dichotomous effect on synovial membrane and articular cartilage COMP in the AIA model. COMP is a useful inflammation marker in the synovial tissue, but it also contributes to the structural integrity of the hyaline articular cartilage forming bridges between type II and IX collagens. Enhancement of COMP in clodronate treated AIA cartilage suggests a chondroprotective and anti-inflammatory effect in the inflammatorily damaged and mechanically strained cartilage.</description><identifier>ISSN: 0392-856X</identifier><identifier>EISSN: 1593-098X</identifier><identifier>PMID: 17207376</identifier><language>eng</language><publisher>Pisa: Clinical and Experimental Rheumatology</publisher><subject>Animals ; Arthritis, Experimental - drug therapy ; Arthritis, Experimental - etiology ; Arthritis, Experimental - metabolism ; Biological and medical sciences ; Bone Density Conservation Agents - administration &amp; dosage ; Bone Density Conservation Agents - pharmacology ; Bones, joints and connective tissue. 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Antiinflammatory agents</subject><subject>Cartilage, Articular - drug effects</subject><subject>Cartilage, Articular - metabolism</subject><subject>Cartilage, Articular - pathology</subject><subject>Clodronic Acid - administration &amp; dosage</subject><subject>Clodronic Acid - pharmacology</subject><subject>Disease Models, Animal</subject><subject>Diseases of the osteoarticular system</subject><subject>Extracellular Matrix Proteins - immunology</subject><subject>Extracellular Matrix Proteins - metabolism</subject><subject>Glycoproteins - immunology</subject><subject>Glycoproteins - metabolism</subject><subject>Immunoglobulin G - immunology</subject><subject>Injections, Intra-Articular</subject><subject>Liposomes</subject><subject>Matrilin Proteins</subject><subject>Medical sciences</subject><subject>Miscellaneous. Osteoarticular involvement in other diseases</subject><subject>Pharmacology. 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Antiinflammatory agents</topic><topic>Cartilage, Articular - drug effects</topic><topic>Cartilage, Articular - metabolism</topic><topic>Cartilage, Articular - pathology</topic><topic>Clodronic Acid - administration &amp; dosage</topic><topic>Clodronic Acid - pharmacology</topic><topic>Disease Models, Animal</topic><topic>Diseases of the osteoarticular system</topic><topic>Extracellular Matrix Proteins - immunology</topic><topic>Extracellular Matrix Proteins - metabolism</topic><topic>Glycoproteins - immunology</topic><topic>Glycoproteins - metabolism</topic><topic>Immunoglobulin G - immunology</topic><topic>Injections, Intra-Articular</topic><topic>Liposomes</topic><topic>Matrilin Proteins</topic><topic>Medical sciences</topic><topic>Miscellaneous. Osteoarticular involvement in other diseases</topic><topic>Pharmacology. Drug treatments</topic><topic>Rabbits</topic><topic>Synovial Membrane - drug effects</topic><topic>Synovial Membrane - metabolism</topic><topic>Synovial Membrane - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GOMEZ-BARRENA, E</creatorcontrib><creatorcontrib>LINDROOS, L</creatorcontrib><creatorcontrib>CEPORNS, A</creatorcontrib><creatorcontrib>LOPEZ-FRANCO, M</creatorcontrib><creatorcontrib>SANCHEZ-PERNAUTE, O</creatorcontrib><creatorcontrib>MONKKONEN, J</creatorcontrib><creatorcontrib>SALO, J</creatorcontrib><creatorcontrib>HERRERO-BEAUMONT, G</creatorcontrib><creatorcontrib>KONTTINEN, Y</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and experimental rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GOMEZ-BARRENA, E</au><au>LINDROOS, L</au><au>CEPORNS, A</au><au>LOPEZ-FRANCO, M</au><au>SANCHEZ-PERNAUTE, O</au><au>MONKKONEN, J</au><au>SALO, J</au><au>HERRERO-BEAUMONT, G</au><au>KONTTINEN, Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cartilage oligomeric matrix protein (COMP) is modified by intra-articular liposomal clodronate in an experimental model of arthritis</atitle><jtitle>Clinical and experimental rheumatology</jtitle><addtitle>Clin Exp Rheumatol</addtitle><date>2006-11-01</date><risdate>2006</risdate><volume>24</volume><issue>6</issue><spage>622</spage><epage>628</epage><pages>622-628</pages><issn>0392-856X</issn><eissn>1593-098X</eissn><abstract>High-dose liposomal bisphosphonates exert apoptotic effects. 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Low-dose, non-cytotoxic liposomal clodronate exerts a dichotomous effect on synovial membrane and articular cartilage COMP in the AIA model. COMP is a useful inflammation marker in the synovial tissue, but it also contributes to the structural integrity of the hyaline articular cartilage forming bridges between type II and IX collagens. Enhancement of COMP in clodronate treated AIA cartilage suggests a chondroprotective and anti-inflammatory effect in the inflammatorily damaged and mechanically strained cartilage.</abstract><cop>Pisa</cop><pub>Clinical and Experimental Rheumatology</pub><pmid>17207376</pmid><tpages>7</tpages></addata></record>
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identifier ISSN: 0392-856X
ispartof Clinical and experimental rheumatology, 2006-11, Vol.24 (6), p.622-628
issn 0392-856X
1593-098X
language eng
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source MEDLINE; Alma/SFX Local Collection
subjects Animals
Arthritis, Experimental - drug therapy
Arthritis, Experimental - etiology
Arthritis, Experimental - metabolism
Biological and medical sciences
Bone Density Conservation Agents - administration & dosage
Bone Density Conservation Agents - pharmacology
Bones, joints and connective tissue. Antiinflammatory agents
Cartilage, Articular - drug effects
Cartilage, Articular - metabolism
Cartilage, Articular - pathology
Clodronic Acid - administration & dosage
Clodronic Acid - pharmacology
Disease Models, Animal
Diseases of the osteoarticular system
Extracellular Matrix Proteins - immunology
Extracellular Matrix Proteins - metabolism
Glycoproteins - immunology
Glycoproteins - metabolism
Immunoglobulin G - immunology
Injections, Intra-Articular
Liposomes
Matrilin Proteins
Medical sciences
Miscellaneous. Osteoarticular involvement in other diseases
Pharmacology. Drug treatments
Rabbits
Synovial Membrane - drug effects
Synovial Membrane - metabolism
Synovial Membrane - pathology
title Cartilage oligomeric matrix protein (COMP) is modified by intra-articular liposomal clodronate in an experimental model of arthritis
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