Van Kolfschoten A A, Hagelen F, Van Noordwijk J
Eur J Pharmacol. 1982 Oct 15;84(1-2):123-5. doi: 10.1016/0014-2999(82)90168-6.
Using ex vivo incubation of mucosal strips the production of prostaglandins (I2- and E-like PGs) in the rat stomach was demonstrated by bioassay. Indomethacin inhibited this PG synthesis 1 and 4 h after oral drug administration. Paracetamol stimulated the production of PGs when given by itself but could not prevent the inhibitory action of indomethacin. Protection of the stomach by paracetamol against the injuring effect of indomethacin is therefore not due to preservation of the production of protective PGs.
利用黏膜条离体孵育,通过生物测定法证实了大鼠胃中前列腺素(I2类和E类前列腺素)的生成。口服吲哚美辛后1小时和4小时,其抑制了这种前列腺素的合成。对乙酰氨基酚单独给药时可刺激前列腺素的生成,但无法阻止吲哚美辛的抑制作用。因此,对乙酰氨基酚对胃的保护作用并非由于保留了具有保护作用的前列腺素的生成,从而免受吲哚美辛的损伤作用。