Cargando…
Danshen attenuates cartilage injuries in osteoarthritis in vivo and in vitro by activating JAK2/STAT3 and AKT pathways
Articular cartilage degradation is a main feature of osteoarthritis (OA). The effects of Danshen, a traditional Chinese herb, in mitigating cartilage damage have been reported before. This study was conducted to investigate the effects of Danshen on cartilage injuries in OA. Rabbit OA models were es...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Association for Laboratory Animal Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955744/ https://www.ncbi.nlm.nih.gov/pubmed/29093428 http://dx.doi.org/10.1538/expanim.17-0062 |
_version_ | 1783323771539554304 |
---|---|
author | Xu, Xilin Lv, Hang Li, Xiaodong Su, Hui Zhang, Xiaofeng Yang, Jun |
author_facet | Xu, Xilin Lv, Hang Li, Xiaodong Su, Hui Zhang, Xiaofeng Yang, Jun |
author_sort | Xu, Xilin |
collection | PubMed |
description | Articular cartilage degradation is a main feature of osteoarthritis (OA). The effects of Danshen, a traditional Chinese herb, in mitigating cartilage damage have been reported before. This study was conducted to investigate the effects of Danshen on cartilage injuries in OA. Rabbit OA models were established by surgical destabilization of the medial meniscus and the anterior and posterior cruciate ligaments in the left knee joint. Injection of Danshen into the articular cavity attenuated OA cartilage destruction in vivo. The levels of phosphorylated Janus kinase 2 (JAK2) and phosphorylated signal transducer and activator of transcription 3 (STAT3) were decreased in osteoarthritic cartilage, while they were rescued upon Danshen treatment. Furthermore, chondrocytes isolated from normal rabbit cartilage were exposed to 2 mM sodium nitroprusside (SNP) to establish an OA model in vitro. We found that the oxidative stress and chondrocyte apoptosis induced by SNP were suppressed by Danshen. The phosphorylation levels of JAK2 and STAT3 were decreased in response to SNP treatment, whereas they were rescued by Danshen. Additionally, AG490, a specific JAK2 inhibitor, counteracted the anti-apoptotic effect of Danshen. The phosphorylation level of protein kinase B (AKT) was also altered in response to SNP and reversed by Danshen. The anti-apoptotic effect of Danshen was counteracted by AKT pathway inhibitor LY194002. Taken together, Danshen attenuates OA cartilage destruction by regulating the JAK2/STAT3 and AKT signaling pathways. |
format | Online Article Text |
id | pubmed-5955744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Japanese Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-59557442018-05-21 Danshen attenuates cartilage injuries in osteoarthritis in vivo and in vitro by activating JAK2/STAT3 and AKT pathways Xu, Xilin Lv, Hang Li, Xiaodong Su, Hui Zhang, Xiaofeng Yang, Jun Exp Anim Original Articular cartilage degradation is a main feature of osteoarthritis (OA). The effects of Danshen, a traditional Chinese herb, in mitigating cartilage damage have been reported before. This study was conducted to investigate the effects of Danshen on cartilage injuries in OA. Rabbit OA models were established by surgical destabilization of the medial meniscus and the anterior and posterior cruciate ligaments in the left knee joint. Injection of Danshen into the articular cavity attenuated OA cartilage destruction in vivo. The levels of phosphorylated Janus kinase 2 (JAK2) and phosphorylated signal transducer and activator of transcription 3 (STAT3) were decreased in osteoarthritic cartilage, while they were rescued upon Danshen treatment. Furthermore, chondrocytes isolated from normal rabbit cartilage were exposed to 2 mM sodium nitroprusside (SNP) to establish an OA model in vitro. We found that the oxidative stress and chondrocyte apoptosis induced by SNP were suppressed by Danshen. The phosphorylation levels of JAK2 and STAT3 were decreased in response to SNP treatment, whereas they were rescued by Danshen. Additionally, AG490, a specific JAK2 inhibitor, counteracted the anti-apoptotic effect of Danshen. The phosphorylation level of protein kinase B (AKT) was also altered in response to SNP and reversed by Danshen. The anti-apoptotic effect of Danshen was counteracted by AKT pathway inhibitor LY194002. Taken together, Danshen attenuates OA cartilage destruction by regulating the JAK2/STAT3 and AKT signaling pathways. Japanese Association for Laboratory Animal Science 2017-10-31 2018 /pmc/articles/PMC5955744/ /pubmed/29093428 http://dx.doi.org/10.1538/expanim.17-0062 Text en ©2018 Japanese Association for Laboratory Animal Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Original Xu, Xilin Lv, Hang Li, Xiaodong Su, Hui Zhang, Xiaofeng Yang, Jun Danshen attenuates cartilage injuries in osteoarthritis in vivo and in vitro by activating JAK2/STAT3 and AKT pathways |
title | Danshen attenuates cartilage injuries in osteoarthritis in
vivo and in vitro by activating JAK2/STAT3 and AKT
pathways |
title_full | Danshen attenuates cartilage injuries in osteoarthritis in
vivo and in vitro by activating JAK2/STAT3 and AKT
pathways |
title_fullStr | Danshen attenuates cartilage injuries in osteoarthritis in
vivo and in vitro by activating JAK2/STAT3 and AKT
pathways |
title_full_unstemmed | Danshen attenuates cartilage injuries in osteoarthritis in
vivo and in vitro by activating JAK2/STAT3 and AKT
pathways |
title_short | Danshen attenuates cartilage injuries in osteoarthritis in
vivo and in vitro by activating JAK2/STAT3 and AKT
pathways |
title_sort | danshen attenuates cartilage injuries in osteoarthritis in
vivo and in vitro by activating jak2/stat3 and akt
pathways |
topic | Original |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955744/ https://www.ncbi.nlm.nih.gov/pubmed/29093428 http://dx.doi.org/10.1538/expanim.17-0062 |
work_keys_str_mv | AT xuxilin danshenattenuatescartilageinjuriesinosteoarthritisinvivoandinvitrobyactivatingjak2stat3andaktpathways AT lvhang danshenattenuatescartilageinjuriesinosteoarthritisinvivoandinvitrobyactivatingjak2stat3andaktpathways AT lixiaodong danshenattenuatescartilageinjuriesinosteoarthritisinvivoandinvitrobyactivatingjak2stat3andaktpathways AT suhui danshenattenuatescartilageinjuriesinosteoarthritisinvivoandinvitrobyactivatingjak2stat3andaktpathways AT zhangxiaofeng danshenattenuatescartilageinjuriesinosteoarthritisinvivoandinvitrobyactivatingjak2stat3andaktpathways AT yangjun danshenattenuatescartilageinjuriesinosteoarthritisinvivoandinvitrobyactivatingjak2stat3andaktpathways |