Kubota T, Komatsu H, Kawamoto H, Yamada T
Arch Int Pharmacodyn Ther. 1979 Jan;237(1):169-76.
Effects of ketoprofen, indomethacin, phenylbutazone and acetylsalicylic acid on edema and on in vivo and in vitro synthesis of PGE1, PGE2 and PGF2 alpha in response to carrageenin were studied in rats. Ketoprofen was a potent drug in depressing edema and increased PGE1, PGE2 and PGF2 alpha in response to carrageenin. Ketoprofen also inhibited in vitro synthesis of PGE2 and PGF2 alpha from arachidonic acid. The relative potency of ketoprofen in those parameters was comparable to or greater than that of indomethacin. Phenylbutazone and acetyl-salicylic acid were, however, less potent in this respect. It is suggested that ketoprofen manifests its anti-inflammatory action, at least in part, by inhibiting prostaglandin synthesis.
在大鼠中研究了酮洛芬、吲哚美辛、保泰松和乙酰水杨酸对角叉菜胶所致水肿以及对PGE1、PGE2和PGF2α体内外合成的影响。酮洛芬是一种强效药物,可减轻水肿,并增加角叉菜胶刺激下的PGE1、PGE2和PGF2α。酮洛芬还抑制花生四烯酸体外合成PGE2和PGF2α。酮洛芬在这些参数方面的相对效力与吲哚美辛相当或更强。然而,保泰松和乙酰水杨酸在这方面效力较弱。提示酮洛芬至少部分通过抑制前列腺素合成来发挥其抗炎作用。