Effects of low molecular weight hyaluronan combined with carprofen on canine osteoarthritis articular chondrocytes and cartilage explants in vitro
© 2015, The Society for In Vitro Biology. Intra-articular injection with non-steroidal anti-inflammatory drugs (NSAIDs) is used to treat inflammatory joint disease, but the side effects of NSAIDs include chondrotoxicity. Hyaluronan has shown positive effects on chondrocytes by reducing apoptosis and...
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th-cmuir.6653943832-541182018-09-04T10:07:56Z Effects of low molecular weight hyaluronan combined with carprofen on canine osteoarthritis articular chondrocytes and cartilage explants in vitro Thippaporn Euppayo Puntita Siengdee Kittisak Buddhachat Waranee Pradit Nawarat Viriyakhasem Siriwadee Chomdej Siriwan Ongchai Yasuji Harada Korakot Nganvongpanit Biochemistry, Genetics and Molecular Biology © 2015, The Society for In Vitro Biology. Intra-articular injection with non-steroidal anti-inflammatory drugs (NSAIDs) is used to treat inflammatory joint disease, but the side effects of NSAIDs include chondrotoxicity. Hyaluronan has shown positive effects on chondrocytes by reducing apoptosis and increasing proteoglycan synthesis. The purposes of this study were to evaluate the effects of low molecular weight hyaluronan (low MW HA), carprofen 25 mg/ml, carprofen 12.5 mg/ml, and a combination of HA and carprofen on canine osteoarthritis (OA) articular chondrocytes and a cartilage explant model in terms of cell viability, extracellular matrix remaining, and gene expression after exposure. In chondrocyte culture, MTT assay was used to evaluate the chondrotoxicity of IC<inf>50</inf> and IC<inf>80</inf> of carprofen with HA. In cartilage explant culture, two kinds of extracellular matrix (uronic acid and collagen) remaining in cartilage were used to evaluate cartilage damage for 14 d after treatment. Expression of COL2A1, AGG, and MMP3 was used to evaluate the synthesis and degradation of the matrix for 7 d after treatment. In chondrocyte culture, low MW HA could preserve OA chondrocyte viability but could not reduce the chondrotoxicity level of carprofen (P < 0.05). In explant culture, low MW HA combined with 12.5 mg/ml carprofen caused less destruction of uronic acid and collagen structure when compared with the control (P < 0.05). Low MW HA caused high expression levels of COL2A1 and AGG in OA cartilage (P < 0.05); HA combined with carprofen resulted in higher COL2A1 and AGG expression levels than carprofen alone. 2018-09-04T10:07:56Z 2018-09-04T10:07:56Z 2015-09-25 Journal 10712690 2-s2.0-84942200275 10.1007/s11626-015-9908-9 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84942200275&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/54118 |
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Biochemistry, Genetics and Molecular Biology Thippaporn Euppayo Puntita Siengdee Kittisak Buddhachat Waranee Pradit Nawarat Viriyakhasem Siriwadee Chomdej Siriwan Ongchai Yasuji Harada Korakot Nganvongpanit Effects of low molecular weight hyaluronan combined with carprofen on canine osteoarthritis articular chondrocytes and cartilage explants in vitro |
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© 2015, The Society for In Vitro Biology. Intra-articular injection with non-steroidal anti-inflammatory drugs (NSAIDs) is used to treat inflammatory joint disease, but the side effects of NSAIDs include chondrotoxicity. Hyaluronan has shown positive effects on chondrocytes by reducing apoptosis and increasing proteoglycan synthesis. The purposes of this study were to evaluate the effects of low molecular weight hyaluronan (low MW HA), carprofen 25 mg/ml, carprofen 12.5 mg/ml, and a combination of HA and carprofen on canine osteoarthritis (OA) articular chondrocytes and a cartilage explant model in terms of cell viability, extracellular matrix remaining, and gene expression after exposure. In chondrocyte culture, MTT assay was used to evaluate the chondrotoxicity of IC<inf>50</inf> and IC<inf>80</inf> of carprofen with HA. In cartilage explant culture, two kinds of extracellular matrix (uronic acid and collagen) remaining in cartilage were used to evaluate cartilage damage for 14 d after treatment. Expression of COL2A1, AGG, and MMP3 was used to evaluate the synthesis and degradation of the matrix for 7 d after treatment. In chondrocyte culture, low MW HA could preserve OA chondrocyte viability but could not reduce the chondrotoxicity level of carprofen (P < 0.05). In explant culture, low MW HA combined with 12.5 mg/ml carprofen caused less destruction of uronic acid and collagen structure when compared with the control (P < 0.05). Low MW HA caused high expression levels of COL2A1 and AGG in OA cartilage (P < 0.05); HA combined with carprofen resulted in higher COL2A1 and AGG expression levels than carprofen alone. |
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Thippaporn Euppayo Puntita Siengdee Kittisak Buddhachat Waranee Pradit Nawarat Viriyakhasem Siriwadee Chomdej Siriwan Ongchai Yasuji Harada Korakot Nganvongpanit |
author_facet |
Thippaporn Euppayo Puntita Siengdee Kittisak Buddhachat Waranee Pradit Nawarat Viriyakhasem Siriwadee Chomdej Siriwan Ongchai Yasuji Harada Korakot Nganvongpanit |
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Thippaporn Euppayo |
title |
Effects of low molecular weight hyaluronan combined with carprofen on canine osteoarthritis articular chondrocytes and cartilage explants in vitro |
title_short |
Effects of low molecular weight hyaluronan combined with carprofen on canine osteoarthritis articular chondrocytes and cartilage explants in vitro |
title_full |
Effects of low molecular weight hyaluronan combined with carprofen on canine osteoarthritis articular chondrocytes and cartilage explants in vitro |
title_fullStr |
Effects of low molecular weight hyaluronan combined with carprofen on canine osteoarthritis articular chondrocytes and cartilage explants in vitro |
title_full_unstemmed |
Effects of low molecular weight hyaluronan combined with carprofen on canine osteoarthritis articular chondrocytes and cartilage explants in vitro |
title_sort |
effects of low molecular weight hyaluronan combined with carprofen on canine osteoarthritis articular chondrocytes and cartilage explants in vitro |
publishDate |
2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84942200275&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/54118 |
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