Shaw Jiajiu, Chen Ben, Wooley Paul, Huang Wen-Hsin, Lee An-Rong, Zeng Dustin
Unitech Pharmaceuticals, Inc., Ann Arbor, MI 48108, USA.
Am J Biomed Sci. 2011 Jan 1;3(1):31-39. doi: 10.5099/aj110100031.
Rheumatoid arthritis (RA) is a common disease characterized by chronic inflammation and irreversible destruction of articular cartilage and bone. In this report, we examined the anti-inflammatory and anti-arthritic effects of a novel leflunomide analogue, UTL-5b (also known as GBL-5b), for potential RA treatment. Using a carrageenan-induced edema study in rats, UTL-5b exhibited a better anti-inflammatory effect as compared with leflunomide and its metabolite. The chronic efficacy of UTL-5b was examined using type II collagen-induced arthritis (CIA) mouse model. UTL-5b exerted an anti-arthritic effect in a dose-dependant manner with mice given 30 mg/kg exhibiting amelioration of disease early in the trial, but losing statistical significance over time. In contrast, mice treated with 60 mg/kg showed reduced clinical disease parameters early in the trial and these effects were sustained over the ten week trial period. Mechanistic studies indicate that UTL-5b is an inhibitor of TNF-α production in vivo. Oral administration of UTL-5b prior to i.p. injection with lethal dose of lipopolysaccharide (LPS)/D-galactosamine markedly reduced the levels of serum TNF-α and increased survival rates of animals from septic shock-induced death. Acute toxicity study using mice receiving increasing doses of UTL-5b showed that no animals were killed by UTL-5b at 2,000 mg/kg (LD(50) >2,000 mg/kg). Our studies show that UTL-5b represents a novel anti-inflammatory and anti-arthritic agent with potential therapeutic application for RA treatment.
类风湿性关节炎(RA)是一种常见疾病,其特征为关节软骨和骨骼的慢性炎症及不可逆破坏。在本报告中,我们研究了一种新型来氟米特类似物UTL-5b(也称为GBL-5b)对类风湿性关节炎的潜在治疗作用,考察其抗炎和抗关节炎效果。在大鼠角叉菜胶诱导的水肿实验中,与来氟米特及其代谢产物相比,UTL-5b表现出更好的抗炎效果。使用II型胶原诱导的关节炎(CIA)小鼠模型考察UTL-5b的慢性疗效。UTL-5b以剂量依赖方式发挥抗关节炎作用,给予30 mg/kg的小鼠在试验早期疾病有所改善,但随着时间推移失去统计学意义。相比之下,给予60 mg/kg的小鼠在试验早期临床疾病参数降低,且这些效果在为期十周的试验期内持续存在。机制研究表明,UTL-5b是体内肿瘤坏死因子-α(TNF-α)产生的抑制剂。在腹腔注射致死剂量的脂多糖(LPS)/D-半乳糖胺之前口服UTL-5b,可显著降低血清TNF-α水平,并提高动物因脓毒性休克诱导死亡的存活率。对接受递增剂量UTL-5b的小鼠进行的急性毒性研究表明,在2000 mg/kg剂量下无动物被UTL-5b致死(半数致死量>2000 mg/kg)。我们的研究表明,UTL-5b是一种新型抗炎和抗关节炎药物,对类风湿性关节炎治疗具有潜在的治疗应用价值。