Magnusson C, Selstam G, Ahrén K
Acta Physiol Scand. 1979 Feb;105(2):239-47. doi: 10.1111/j.1748-1716.1979.tb06336.x.
Prostaglandins (PGs) have been proposed to function as obligatory intermediates in the action of luteinizing hormone (LH) (Kuehl et al. 1970). This based on experiments on isolated mouse ovaries where the substance 7-oxa-13-prostynoic acid (7-oxa-13-PA) was found to block the effect of both PGE1 and LH on ovarian cyclic AMP formation and progesterone synthesis. We have studied whether 7-oxa-13-PA acts as a PG antagonist also on the isolated rat ovary, where PGs of the E type have many effects. Prepubertal rat ovaries were incubated up to 4 h in modified Krebs bicarbonate buffer containing glucose with PGE1 and 7-oxa-13-PA, alone and in combination. PGE1 stimulated the uptake of the non-utilizable amino acids alpha-aminoisobutyric acid (AIB) and cycloleucine in an equally wide dose-range as has earlier been found for the stimulation of lactic acid and cyclic AMP production as well as protein synthesis. 7-oxa-13-PA alone, in concentrations exceeding 25 microgram/ml, stimulated lactic acid production, but inhibited the incorporation of labelled leucine and the uptake of AIB. The uptake of cycloleucine was slightly stimulated. 7-oxa-13-PA did not antagonize the PGE1 effect on lactic acid production. 7-oxa-13-PA diminished the PGE1 effect on the uptake of amino acids and the incorporation into protein, but only in concentrations where it in itself inhibited the protein synthesis. These results show that 7-oxa-13-PA does not act as a PG-antagonist in the prepubertal rat ovary, since it cannot block the effects of PGs without having marked inherent effects.
前列腺素(PGs)被认为是促黄体生成素(LH)作用过程中的必需中间体(Kuehl等人,1970年)。这是基于对分离的小鼠卵巢进行的实验得出的,实验发现7-氧杂-13-前列腺炔酸(7-oxa-13-PA)能阻断PGE1和LH对卵巢环磷酸腺苷(cAMP)形成及孕酮合成的影响。我们研究了7-氧杂-13-PA在分离的大鼠卵巢上是否也作为PG拮抗剂起作用,在大鼠卵巢中E型PG有多种作用。将青春期前大鼠卵巢在含有葡萄糖的改良Krebs碳酸氢盐缓冲液中与PGE1和7-氧杂-13-PA单独及联合孵育长达4小时。PGE1在与先前发现的刺激乳酸、环磷酸腺苷产生以及蛋白质合成相同的宽剂量范围内刺激了不可利用氨基酸α-氨基异丁酸(AIB)和环亮氨酸的摄取。单独的7-氧杂-13-PA,浓度超过25微克/毫升时,刺激了乳酸产生,但抑制了标记亮氨酸的掺入和AIB的摄取。环亮氨酸的摄取略有刺激。7-氧杂-13-PA并未拮抗PGE1对乳酸产生的作用。7-氧杂-13-PA减弱了PGE1对氨基酸摄取和掺入蛋白质的作用,但仅在其本身抑制蛋白质合成的浓度下才如此。这些结果表明,7-氧杂-13-PA在青春期前大鼠卵巢中不作为PG拮抗剂起作用,因为它在没有明显固有作用的情况下无法阻断PG的作用。