Woclawek-Potocka Izabela, Kowalczyk-Zieba Ilona, Skarzynski Dariusz Jan
Department of Reproductive Immunology and Pathology, Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Poland.
J Reprod Dev. 2010 Aug;56(4):411-20. doi: 10.1262/jrd.09-205k. Epub 2010 Apr 22.
We have previously documented synthesis of lysophosphatidic acid (LPA) in the bovine endometrium and the increased presence of LPA receptor mRNA expression during pregnancy. Therefore, LPA could contribute to early pregnancy establishment in the cow. In the present study, we investigated the effect of intravaginally administered LPA on pregnancy rates and on the plasma levels of progesterone (P4) and prostaglandins (PGs) in heifers. Animals were inseminated and from day 15 to 18 after estrus were treated intravaginally with saline, LPA (1 mg) or LPA receptor blocker (VPC32183; 1 mg). Blood samples were collected on days 0, 6, 12, 15, 16, 17, 18 and 21 after insemination. Pregnancy was confirmed by ultrasonography and per rectum examination on days 30 and 49-50 after insemination. Intravaginal LPA administration increased the plasma P4 and PGE(2) concentrations compared with saline and VPC32183-treated heifers. In the saline and LPA-treated groups, 6 out of 8 heifers were pregnant (75%), whereas the pregnancy rate in the VPC32183-treated heifers was only 37%. We also examined the effects of LPA on PG secretion and PG synthase mRNA expression in stromal and epithelial cells of the bovine endometrium on days 16-18 of pregnancy and the estrous cycle. LPA increased PGE(2) production and PGE(2) synthase (PGES) mRNA expression in stromal cells during the estrous cycle and pregnancy. On Days 16-18 of pregnancy, LPA inhibited PGF(2alpha) production and PGFS mRNA expression in epithelial cells. The results suggest that LPA serves as a luteotropic factor during the estrous cycle and pregnancy, stimulating P4 secretion in vivo and PGE(2) secretion in vitro through activation of PGES mRNA expression in stromal cells. Moreover, during the early pregnancy, LPA decreases PGF(2alpha) synthesis and mRNA expression for PGFS in epithelial cells of the bovine endometrium.
我们之前已记录了牛子宫内膜中溶血磷脂酸(LPA)的合成以及孕期LPA受体mRNA表达的增加。因此,LPA可能有助于奶牛早期妊娠的建立。在本研究中,我们调查了经阴道给予LPA对小母牛妊娠率以及血浆孕酮(P4)和前列腺素(PGs)水平的影响。动物进行授精,在发情后第15至18天经阴道用生理盐水、LPA(1毫克)或LPA受体阻滞剂(VPC32183;1毫克)进行处理。在授精后第0、6、12、15、16、17、18和21天采集血样。在授精后第30天以及第49 - 50天通过超声检查和直肠检查确认妊娠情况。与生理盐水和VPC32183处理的小母牛相比,经阴道给予LPA可提高血浆P4和PGE(2)浓度。在生理盐水和LPA处理组中,8头小母牛中有6头怀孕(75%),而VPC32183处理的小母牛妊娠率仅为37%。我们还研究了在妊娠第16 - 18天和发情周期时LPA对牛子宫内膜基质细胞和上皮细胞中PG分泌及PG合酶mRNA表达的影响。在发情周期和孕期,LPA可增加基质细胞中PGE(2)的产生以及PGE(2)合酶(PGES)mRNA的表达。在妊娠第16 - 18天,LPA可抑制上皮细胞中PGF(2α)的产生以及PGFS mRNA的表达。结果表明,LPA在发情周期和孕期作为一种促黄体因子,通过激活基质细胞中PGES mRNA的表达,在体内刺激P4分泌,在体外刺激PGE(2)分泌。此外,在妊娠早期,LPA可降低牛子宫内膜上皮细胞中PGF(2α)的合成以及PGFS的mRNA表达。