McDougall A N, Walker F M, Watson J
Br J Pharmacol. 1977 Jul;60(3):425-31. doi: 10.1111/j.1476-5381.1977.tb07518.x.
1 Human luteal tissue slices from days 18, 21 and 25 of the menstrual cycle were superfused in vitro with Medium 199 alone or containing cloprostenol (1 microgram/ml). Concentrations of progesterone, oestradiol-17beta and prostaglandins F2alpha and E2 were determined in the superfusate samples. 2 Secretion of steroids and prostaglandins was maintained at an approximately constant level throughout the experiments (21 h in one case) when the tissue was perfused with M199 alone. 3 Superfusion with cloprostenol (1 microgram/ml) resulted in an initial depression of progesterone and oestradiol-17beta but this was not maintained, levels returning to control values or showing an increase, while superfusion with cloprostenol continued. Cloprostenol is not therefore considered to be luteolytic at this dose and under these conditions for human luteal tissue in vitro. 4 Superfusion with cloprostenol (1 microgram/ml) also resulted in a large stimulation of secretion of endogenous prostaglandin F2 alpha following a short lag phase. This stimulation was possibly due to the initial depression of progesterone secretion. A short-lived stimulation of prostaglandin E2 secretion was also observed. 5 The significance of the increase in prostaglandin E2 secretion and the interrelationships between the various changes observed with cloprostenol are difficult to interpret.
取自月经周期第18、21和25天的人黄体组织切片,在体外分别用单纯的199培养基或含氯前列醇(1微克/毫升)的199培养基进行灌流。测定灌流液样品中孕酮、雌二醇-17β以及前列腺素F2α和E2的浓度。
当用单纯的M199培养基对组织进行灌流时,在整个实验过程中(一例为21小时),类固醇和前列腺素的分泌维持在大致恒定的水平。
用氯前列醇(1微克/毫升)灌流导致孕酮和雌二醇-17β最初下降,但这种下降并未持续,随着氯前列醇灌流的继续,水平恢复到对照值或有所升高。因此,在这种剂量和条件下,对于体外培养的人黄体组织,氯前列醇不被认为具有溶黄体作用。
用氯前列醇(1微克/毫升)灌流在短暂的延迟期后还导致内源性前列腺素F2α分泌大量增加。这种增加可能是由于孕酮分泌最初下降所致。还观察到前列腺素E2分泌有短暂的增加。
前列腺素E2分泌增加的意义以及氯前列醇所观察到的各种变化之间的相互关系难以解释。