ANTIINFLAMMATORY AND IMMUNOSUPPRESSIVE EFFECTS OF -3,4-DIDEOXY-2-FURFURYL-BETA-D-THREO-3-ENOPYRANOSE (MT2221), A NOVEL ANHYDRO-ENOPYRANOSE DERIVATIVE, ON EXPERIMENTAL ANIMAL-MODELS
Citation
S. Mizukoshi et al., ANTIINFLAMMATORY AND IMMUNOSUPPRESSIVE EFFECTS OF -3,4-DIDEOXY-2-FURFURYL-BETA-D-THREO-3-ENOPYRANOSE (MT2221), A NOVEL ANHYDRO-ENOPYRANOSE DERIVATIVE, ON EXPERIMENTAL ANIMAL-MODELS, Biological & pharmaceutical bulletin, 17(8), 1994, pp. 1070-1074
Categorie Soggetti
Pharmacology & Pharmacy
SICI code
0918-6158(1994)17:8<1070:AAIEO->2.0.ZU;2-U
Abstract
The anti-inflammatory effects of -3,4-dideoxy-2-furfuryl-beta-D-threo-
3-enopyranose (MT2221) were investigated using animal models and compa
red with the effects of dexamethasone (DEX) and cyclosporin A ((CYA).
MT2221 inhibited carrageenan-induced acute inflammation and adjuvant a
rthritis 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 othe
r inflammation models. The MT2221 mode of action differed from those o
f conventional non-steroidal anti-inflammatory drugs (NSAIDs) and dise
ase modifying anti-rheumatic drugs (DMARDs). All of these drugs are ef
fective against acute inflammation or adjuvant arthritis models, but n
ot against murine CIA. DEX and CYA did inhibit murine CIA, but in othe
r animal models, their mode of action differed from that of MT2221. Mo
reover, allograft transplantation in mice showed that MT2221 slightly
prolonged the allograft survival time. These results suggest that MT22
21 has not only anti-inflammatory but also immunosuppressive effects b
ased upon a novel mechanism of action that is different from NSAIDs, D
MARDs, DEX and CYA.