Poyser N L
J Reprod Fertil. 1985 Sep;75(1):223-30. doi: 10.1530/jrf.0.0750223.
TMB-8, an intracellular Ca2+ antagonist, inhibited the A23187-induced increase in outputs of prostaglandin (PG) F-2 alpha and 6-keto-PGF-1 alpha from the guinea-pig uterus superfused in vitro. The high basal output of PGF-2 alpha from the Day-15 guinea-pig uterus was not inhibited by TMB-8, indicating that a maintained high intracellular free Ca2+ concentration is not necessary for maintaining this high output of PGF-2 alpha. W-7, a calmodulin antagonist, had similar actions except that PGF-2 alpha output from the Day-15 uterus was reduced 20-30 min after the W-7 treatment had stopped. Overall, these findings suggest that, in the guinea-pig, oestradiol acting on a progesterone-primed uterus causes a prolonged stimulation of endometrial phospholipase A-2 in the absence of a maintained high Ca2+ concentration, thus providing a continuous release of arachidonic acid for increased endometrial PGF-2 alpha synthesis during the last third of the oestrous cycle.
细胞内钙离子拮抗剂TMB - 8抑制了A23187诱导的、来自体外灌注的豚鼠子宫的前列腺素(PG)F - 2α和6 - 酮 - PGF - 1α输出量的增加。来自妊娠第15天豚鼠子宫的PGF - 2α的高基础输出量未被TMB - 8抑制,这表明维持高细胞内游离钙离子浓度对于维持这种高PGF - 2α输出量并非必要。钙调蛋白拮抗剂W - 7具有类似作用,只是在停止W - 7处理后20 - 30分钟,来自妊娠第15天子宫的PGF - 2α输出量有所降低。总体而言,这些发现表明,在豚鼠中,作用于经孕酮预处理子宫的雌二醇在不存在维持的高钙离子浓度的情况下,会导致对子宫内膜磷脂酶A - 2的长期刺激,从而在发情周期的最后三分之一期间为增加子宫内膜PGF - 2α合成持续释放花生四烯酸。