Antirheumatic agents and leukocyte recruitment. New light on the mechanism of action of oxaceprol.
Biochem Pharmacol
; 58(2): 209-15, 1999 Jul 15.
Article
en En
| MEDLINE
| ID: mdl-10423160
ABSTRACT
Most anti-inflammatory agents used in the treatment of joint diseases exert inhibitory effects on leukocyte infiltration. Methotrexate, a disease-modifying drug, and corticosteroids also inhibit leukocyte accumulation during inflammation. However, the mechanisms of action of these different compounds on leukocytes vary and in the case of non-steroidal anti-inflammatory drugs (NSAIDs) the mechanism(s) may be indirect. No current drug for inflammatory or degenerative joint disease has been proposed to act specifically by an inhibitory action on neutrophilic leukocytes. Oxaceprol is an amino acid derivative that has been used for several years for the treatment of osteoarthritis and rheumatoid arthritis, ameliorating pain and stiffness and showing good gastrointestinal safety, particularly in comparison with NSAIDs. Recent experimental studies have shown that oxaceprol does not inhibit the synthesis of prostaglandins in vitro, but markedly inhibits neutrophil infiltration into the joints of rats with adjuvant arthritis. These results support earlier screening data showing inhibition by oxaceprol of leukocyte infiltration into sites of acute inflammation. In studies on surgical ischemia reperfusion in hamsters in vivo, oxaceprol was an effective inhibitor of leukocyte adhesion and extravasation. It is proposed that oxaceprol represents a therapeutic agent for degenerative and inflammatory joint diseases, which acts predominantly by inhibiting leukocyte adhesion and migration.
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Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Antirreumáticos
/
Hidroxiprolina
/
Artropatías
/
Leucocitos
Límite:
Humans
Idioma:
En
Revista:
Biochem Pharmacol
Año:
1999
Tipo del documento:
Article
País de afiliación:
Alemania