Nakata K, Ashida K, Nakazawa K, Fujiwara M
Pharmacology. 1981;23(2):95-101. doi: 10.1159/000137535.
In studies on prostaglandin (PG) synthetase activity in the guinea pig gallbladder, prostaglandin E2 and F2 alpha (PGE2 and PGF2 alpha) were enzymatically formed from arachidonic acid using the 105,000-g precipitate fraction. The amount of PGE2 synthesized was about four times larger than PGF2 alpha. Indomethacin (1-3 microM) inhibited both the PG synthesis and the contractile response to transmural stimulation in the gallbladder. These findings suggest that the inhibitory effect of indomethacin on the contractility of the gallbladder is related to the inhibition of PG synthesis, and that endogenous PGE2 is involved in the contractility of this tissue.
在对豚鼠胆囊中前列腺素(PG)合成酶活性的研究中,使用105,000克沉淀组分,从花生四烯酸酶促形成前列腺素E2和F2α(PGE2和PGF2α)。合成的PGE2量约为PGF2α的四倍。吲哚美辛(1 - 3 microM)抑制胆囊中的PG合成以及对透壁刺激的收缩反应。这些发现表明,吲哚美辛对胆囊收缩性的抑制作用与PG合成的抑制有关,并且内源性PGE2参与该组织的收缩性。