Mizukoshi S, Tsukamoto M, Tanaka H, Nakamura K, Kato F
Biochemistry Research Laboratory, Central Research Institute, Ishihara Sangyo Kaisha, Ltd., Shiga, Japan.
Biol Pharm Bull. 1994 Aug;17(8):1070-4. doi: 10.1248/bpb.17.1070.
The anti-inflammatory effects of 1,6-anhydro-3,4-dideoxy-2-furfuryl-beta-D-threo-3-enopyranose (MT2221) were investigated using animal models and compared with the effects of dexamethasone (DEX) and cyclosporin A (CYA). MT2221 inhibited carrageenan-induced acute inflammation and adjuvant arthritis in rats, as well as the delayed-type hypersensitive response and collagen-induced arthritis (CIA) in mice. However, it seemed that this compound was more effective against murine CIA than upon the other inflammation models. The MT2221 mode of action differed from those of conventional non-steroidal anti-inflammatory drugs (NSAIDs) and disease modifying anti-rheumatic drugs (DMARDs). All of these drugs are effective against acute inflammation or adjuvant arthritis models, but not against murine CIA. DEX and CYA did inhibit murine CIA, but in other animal models, their mode of action differed from that of MT2221. Moreover, allograft transplantation in mice showed that MT2221 slightly prolonged the allograft survival time. These results suggest that MT2221 has not only anti-inflammatory but also immunosuppressive effects based upon a novel mechanism of action that is different from NSAIDs, DMARDs, DEX and CYA.
使用动物模型研究了1,6-脱水-3,4-二脱氧-2-糠基-β-D-苏式-3-烯吡喃糖(MT2221)的抗炎作用,并与地塞米松(DEX)和环孢素A(CYA)的作用进行了比较。MT2221可抑制角叉菜胶诱导的大鼠急性炎症和佐剂性关节炎,以及小鼠的迟发型超敏反应和胶原诱导的关节炎(CIA)。然而,该化合物似乎对小鼠CIA的作用比对其他炎症模型更有效。MT2221的作用模式不同于传统的非甾体抗炎药(NSAIDs)和改善病情抗风湿药(DMARDs)。所有这些药物对急性炎症或佐剂性关节炎模型有效,但对小鼠CIA无效。DEX和CYA确实能抑制小鼠CIA,但在其他动物模型中,它们的作用模式与MT2221不同。此外,小鼠同种异体移植表明MT2221可略微延长同种异体移植物的存活时间。这些结果表明,MT2221不仅具有抗炎作用,还具有基于一种不同于NSAIDs、DMARDs、DEX和CYA的新作用机制的免疫抑制作用。