Alleviating Effects of AS1892802, a Rho Kinase Inhibitor, on Osteoarthritic Disorders in Rodents

被引:19
作者
Takeshita, Nobuaki [1 ]
Yoshimi, Eiji [1 ]
Hatori, Chie [1 ]
Kumakura, Fumiyo [1 ]
Seki, Nobuo [1 ]
Shimizu, Yasuaki [1 ]
机构
[1] Astellas Pharma Inc, Pharmacol Res Labs, Tsukuba, Ibaraki 3058585, Japan
关键词
osteoarthritis; Rho kinase inhibitor; cartilage; pain; inflammation; DEGENERATIVE JOINT DISEASE; CHONDROGENIC DIFFERENTIATION; NEUROPATHIC PAIN; PROTEIN-KINASE; MOUSE KNEE; RAT MODELS; ACTIVATION; INTERLEUKIN-1-BETA; EXPRESSION; MORPHOLOGY;
D O I
10.1254/jphs.10319FP
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effects of AS 1892802, a selective Rho-associated coiled coil kinase (ROCK) inhibitor, on knee cartilage damage and pain behavior were examined in a rat model of osteoarthritis (OA). Monoiodoacetate (MIA) was intraarticularly injected into the right knee joints of rats. ROCK I and II mRNA levels increased in knee joints of MIA-injected rats. Our newly synthesized ROCK inhibitor, AS1892802, was injected into the ipsilateral knee or administered p.o. for 3 weeks. The compound dose-dependently and significantly inhibited of cartilage damage in the tibial plateau in a dose-dependent manner and decreased the weight distribution deficit associated with MIA injection. In addition, the compound also inhibited bradykinin induced pain responses in normal rats. In vitro, the compound could induce chondrocyte differentiation in a chondrogenic cell line and significantly inhibited IL-1 beta- or bradykinin-induced prostaglandin E-2 production in a synovial cell line. AS1892802 prevents cartilage damage induced by MIA and has analgesic effects in rat pain models, suggesting that AS1892802 may be clinically useful for the treatment of OA.
引用
收藏
页码:481 / 489
页数:9
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