Tanimoto Atsuo, Shinozaki Yuichi, Nozawa Keisuke, Kimoto Yukari, Amano Wataru, Matsuo Akira, Yamaguchi Takayuki, Matsushita Mutsuyoshi
Central Pharmaceutical Research Institute, Japan Tobacco Inc., 1-1 Murasaki-cho, Takatsuki, Osaka, 569-1125, Japan.
BMC Musculoskelet Disord. 2015 Nov 6;16:339. doi: 10.1186/s12891-015-0802-0.
Rheumatoid arthritis (RA) is a chronic inflammatory disease that leads to joint destruction, disability, and decreased quality of life (QOL). Inhibition of Janus kinase (JAK) signaling ameliorates articular inflammation and joint destruction in animal models of RA, but its effects on behaviors indicating well-being are poorly understood. In this study, we evaluated the effect of JAK inhibition on spontaneous locomotor activity in rats with adjuvant-induced arthritis, a rodent model of RA.
Arthritis was induced in male Lewis rats by a single subcutaneous injection of Freund's complete adjuvant. The novel JAK inhibitor JTE-052 was orally administered for 7 days after the onset of arthritis.
Induction of arthritis suppressed the spontaneous locomotor activity of the rats. Administration of JTE-052 completely improved the spontaneous locomotor activity, with partial reductions in articular inflammation and joint destruction. Hyperalgesia and motor functions were also improved, but the efficacy was not complete. However, serum interleukin (IL)-6 levels were completely decreased at 4 h after administration of the first dose of JTE-052.
This study demonstrated that JAK inhibition improved the spontaneous locomotor activity of rats with adjuvant-induced arthritis, in association with amelioration of pain and physical dysfunction as a consequence of suppression of joint inflammation. Moreover, although further studies are needed, there was possible participation of IL-6 downregulation in the improvement of locomotor activity by JAK inhibition.
类风湿关节炎(RA)是一种慢性炎症性疾病,可导致关节破坏、残疾和生活质量(QOL)下降。在RA动物模型中,抑制Janus激酶(JAK)信号可改善关节炎症和关节破坏,但其对表明幸福感的行为的影响尚不清楚。在本研究中,我们评估了JAK抑制对佐剂诱导性关节炎大鼠自发运动活动的影响,佐剂诱导性关节炎是一种RA啮齿动物模型。
通过单次皮下注射弗氏完全佐剂在雄性Lewis大鼠中诱导关节炎。在关节炎发作后口服新型JAK抑制剂JTE-052,持续7天。
关节炎的诱导抑制了大鼠的自发运动活动。给予JTE-052可完全改善自发运动活动,同时关节炎症和关节破坏部分减轻。痛觉过敏和运动功能也有所改善,但效果不完全。然而,在给予第一剂JTE-052后4小时,血清白细胞介素(IL)-6水平完全下降。
本研究表明,JAK抑制改善了佐剂诱导性关节炎大鼠的自发运动活动,同时由于抑制关节炎症而改善了疼痛和身体功能障碍。此外,尽管需要进一步研究,但JAK抑制改善运动活动可能与IL-6下调有关。