Falkay G, Sas M
Horm Res. 1977;8(2):99-106. doi: 10.1159/000178786.
The authors were investigating the metabolism of prostaglandin F2alpha in human early placenta, in in vitro incubation experiments. They have identified both major metabolites, 15-keto-PGF2alpha and 15-keto-13,14 dehydro PGF2alpha. They have examined the change in the percentage of these, taken as a function of time. They have established that the main site of inactivating the endogenous PGF2alpha is the early human placenta. They suppose that the considerable Pg-inactiviting effect of the placenta has a part which acts as a protecting mechanism in preventing the uterotonic influence of the endogenous prostaglandins.
作者们在体外培养实验中研究了前列腺素F2α在人早期胎盘中的代谢情况。他们已鉴定出两种主要代谢产物,即15-酮-前列腺素F2α和15-酮-13,14-脱氢前列腺素F2α。他们研究了这些代谢产物的百分比随时间的变化情况。他们确定内源性前列腺素F2α失活的主要部位是人早期胎盘。他们推测胎盘显著的前列腺素失活作用在防止内源性前列腺素的子宫收缩影响方面起到了一种保护机制的作用。