We examined the ability of the analgesic drug tramadol to affect the develo
pment of inflammation in rats. The acute administration of tramadol signifi
cantly reduced the edema and the hyperalgesia induced by yeast injection in
the paw. Moreover, in the subcutaneous carrageenin-induced inflammation, t
ramadol reduced the amount of the exudate, as well as the prostaglandin (PG
)E-2-like bio- and immunoactivity in the exudate; on the contrary, leukotri
ene (LT)B-4 concentrations in the exudate were not changed. However, tramad
ol did not affect the ability of macrophages to migrate towards the chemota
ctic peptide N-formyl-L-methionil-L-leucyl-L-phenylalanine (FMLP). Our resu
lts suggest that tramadol is able to inhibit the development of different t
ypes of inflammation in the rat without affecting immune mechanisms, and co
ntribute to explain the efficacy of this drug in the treatment of inflammat
ory pain. (C) Elsevier, Paris.