Chudaska C, Diallo R, Schlegel W
Frauenklinik der Westfälischen Wilhelms-Universität, Münster, FRG.
Eicosanoids. 1992;5 Suppl:S48-50.
Isolated rabbit luteal cells from day 6 and 12 of pseudopregnancy were cultured with hCG, EGF, and EGF together with arachidonic acid (AA) in serum-free culture medium for 96 hours. The hCG stimulation of the progesterone (P) synthesis was more pronounced on day 6 then on day 12. EGF alone did not change significantly the production of either P or PGF2 alpha. AA increased the production of PGF2 alpha on day 6 and 12 significantly (3.9-fold on day 6, P < 0.005; 7-fold on day 12, P < 0.001). AA together with EGF increased the level of PGF2 alpha more pronounced when compared with AA alone (7.2-fold on day 6, P < 0.025; 9.8-fold on day 12, P < 0.05). The progesterone production of the cells remained unchanged during EGF exposure. We conclude that EGF together with AA is able to stimulate the PGF2 alpha biosynthesis in cultured rabbit luteal cells. Therefore, EGF could be relevant as an additional regression factor in rabbits. This mechanism seems to be independent from the progesterone synthesis.
将来自假孕第6天和第12天的兔黄体细胞在无血清培养基中与hCG、表皮生长因子(EGF)以及EGF和花生四烯酸(AA)一起培养96小时。hCG对孕酮(P)合成的刺激在第6天比第12天更明显。单独的EGF对P或前列腺素F2α(PGF2α)的产生没有显著改变。AA在第6天和第12天显著增加了PGF2α的产生(第6天增加3.9倍,P < 0.005;第12天增加7倍,P < 0.001)。与单独使用AA相比,AA与EGF一起更显著地增加了PGF2α的水平(第6天增加7.2倍,P < 0.025;第12天增加9.8倍,P < 0.05)。在暴露于EGF期间,细胞的孕酮产生保持不变。我们得出结论,EGF与AA一起能够刺激培养的兔黄体细胞中PGF2α的生物合成。因此,EGF可能作为兔额外的黄体退化因子发挥作用。这种机制似乎独立于孕酮合成。