标题:Low molecular weight xanthan gum for treating osteoarthritis
作者:Han, Guanying; Chen, Qixin; Liu, Fei; Cui, Zan; Shao, Huarong; Liu, Fuyan; Ma, Aibin; Liao, Joshua; Guo, Bin; Guo, Yuewei; Wang, F 更多
作者机构:[Han, Guanying; Cui, Zan; Guo, Bin; Mei, Xifan] Jinzhou Med Univ, Affiliated Hosp 1, Jinzhou 121001, Peoples R China.; [Han, Guanying; Chen, Qixin; 更多
通讯作者:Mei, Xifan
通讯作者地址:[Mei, XF]Jinzhou Med Univ, Affiliated Hosp 1, Jinzhou 121001, Peoples R China;[Wang, FS; Ling, PX]Shandong Univ, Sch Pharmaceut Sci, Jinan 250101, Peo 更多
来源:CARBOHYDRATE POLYMERS
出版年:2017
卷:164
页码:386-395
DOI:10.1016/j.carbpol.2017.01.101
关键词:Xanthan gum; Low molecular weight; Sodium hyaluronate; Osteoarthritis
摘要:Osteoarthritis (OA) is one of the most common chronic diseases and characterized by degradation of articular cartilage. We have previously reported xanthan gum (XG) injection preparation with high molecular weights (Mw) in ranging from 3 x 10(6) Da to 5 x 10(6) Da (HM-XG) could enhance the viscosity of synovial fluid, protect joint cartilage in rabbit, and the therapeutical effect has no significance difference with an existing clinical medication (sodium hyaluronate, SH) at the same injection frequency (once weekly for 5 weeks). Herein, we prepared a XG injection preparation with a low Mw (LM-XG) in ranging from 1 x 10(6) Da to 1.5 x 10(6) Da, and evaluated the therapeutical effect for OA therapy at once every 2 weeks for 5 weeks with an SH at once weekly for 5 weeks as reference. The model of OA was induced using anterior cruciate ligament transection (ACLT) in a rabbit in vivo and also using sodium nitroprusside (SNP) in cell culture in vitro. The results showed that LW-XG could also protect cartilage from damage, decrease the concentration of nitric oxide (NO) in synovial fluid and reverse the amplification of the knee joint width similar to HM-XG as our previously reported. At the cellular level, LW-XG promotes proliferation while decreases apoptosis of chondrocytes. Mechanistically at the molecular level, these effects are elicited via down-regulation of the protein levels of caspase-3 and bax and up-regulation of the protein levels of bcl-2 in cartilage in both in vivo and in vitro. These results showed that LW-XG maybe become an excellent candidate long-acting drug for treating OA. (C) 2017 Published by Elsevier Ltd.
收录类别:EI;SCOPUS;SCIE
WOS核心被引频次:4
Scopus被引频次:7
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85013218877&doi=10.1016%2fj.carbpol.2017.01.101&partnerID=40&md5=85ebd273bbc3f8fbcda0d9f24c4d53b2
TOP