Sananès N, Baulieu E E, Le Goascogne C
J Endocrinol. 1981 Apr;89(1):25-33. doi: 10.1677/joe.0.0890025.
The deciduogenic action of various kinds of prostaglandin (PG), i.e. PGE1, PGE2, PGF2 alpha and PGI2, methylated prostaglandins (15-met-PGE1, 15-met-PGE2 and 15-met-PGF2 alpha), PGF2 alpha-13-dehydro analogues (13-DH-PGF2 alpha, ent-15-epi-13-DH-PGF2 alpha), endoperoxide analogues (15S)-hydroxy-9 alpha,11 alpha-(epoxymethano)-prosta-5Z,13E-dienoic acid (U 44069) and (15S)-hydroxy-11 alpha,9 alpha-(epoxymethano)-prosta-5Z, 13E-dienoic acid (U 46619), and of the prostaglandin precursor, arachidonic acid, has been demonstrated after intraluminal instillation of these compounds into the uterus of immature rats sensitized with progesterone alone. Under this minimal hormonal stimulation, in which a trauma (a scratch) of the endometrium is required to induce the decidual response, all these compounds elicited the formation of deciduomata, substantiating the suggestion that the scratch-induced decidual reaction is mediated through release of prostaglandin. Confirmation was obtained through the effect of indomethacin and cortisol, both of which decreased the decidual response brought on by a scratch or by arachidonic acid, whereas the effect of PGF2 alpha was decreased by indomethacin but not by cortisol. Histamine, thromboxane B2, and oleic, palmitic and homo-gamma-linolenic acids were not deciduogenic. A dose-dependent inhibitory effect of indomethacin on deciduoma formation by instillation of oil into animals sensitized by progesterone plus oestradiol was also observed. The results support the proposal that the decidual reaction involves prostaglandins and we suggest that the deciduoma is a valuable model for studying the action of prostaglandin-related compounds.
在仅用孕酮致敏的未成熟大鼠子宫内管腔内滴注各种前列腺素(PG),即PGE1、PGE2、PGF2α和PGI2、甲基化前列腺素(15-甲基-PGE1、15-甲基-PGE2和15-甲基-PGF2α)、PGF2α-13-脱氢类似物(13-DH-PGF2α、对映-15-表-13-DH-PGF2α)、内过氧化物类似物(15S)-羟基-9α,11α-(环氧甲叉基)-前列腺-5Z,13E-二烯酸(U 44069)和(15S)-羟基-11α,9α-(环氧甲叉基)-前列腺-5Z,13E-二烯酸(U 46619)以及前列腺素前体花生四烯酸后,已证实它们具有蜕膜生成作用。在这种最小激素刺激下,即需要子宫内膜创伤(划痕)来诱导蜕膜反应,所有这些化合物均引发了蜕膜瘤的形成,证实了划痕诱导的蜕膜反应是通过前列腺素释放介导的这一观点。通过吲哚美辛和皮质醇的作用得到了证实,二者均降低了划痕或花生四烯酸引起的蜕膜反应,而吲哚美辛降低了PGF2α的作用,但皮质醇未降低。组胺、血栓素B2以及油酸、棕榈酸和同型γ-亚麻酸不具有蜕膜生成作用。还观察到吲哚美辛对在孕酮加雌二醇致敏的动物中滴注油所形成的蜕膜瘤具有剂量依赖性抑制作用。这些结果支持了蜕膜反应涉及前列腺素的观点,并且我们认为蜕膜瘤是研究前列腺素相关化合物作用的一个有价值的模型。