Department of OBGYN, Faculty of Veterinary Medicine, Selcuk University, Konya, Turkey.
Anim Reprod Sci. 2010 Oct;122(1-2):124-32. doi: 10.1016/j.anireprosci.2010.08.007. Epub 2010 Aug 13.
The aim was to evaluate expression of genes involved in the biosynthesis of prostaglandins (PTG), Prostaglandin H Synthase-1 (PTGS1) and PTGS2, PGF synthase (PTGFS), and PGE synthase (PTGES), PGF receptor (PTGFR), PGE receptors (PTGER2 and PTGER4), prostaglandin transporter (SLCO2A1) and hydroxyprostaglandin dehydrogenase-15 (HPGD). Endometrial biopsies were obtained from mares on day of ovulation (d0, n=4), late diestrus (LD, n=4), early luteolysis (EL, n=4) and after luteolysis (AL, n=4) during the cycle. Stages of the cycle were confirmed by plasma progesterone concentrations measured daily and ultrasound examinations. Biopsies were also taken on days 14 (P14; n=4), 15 (P15, n=4), 18 (P18, n=4) and 22 (P22; n=4) of pregnancy. Relative mRNA expressions were quantified using real-time RT-PCR. A mixed model was fitted on the normalized data and least significant difference test (α=0.05) was employed. Expression of PTGS1 mRNA was low throughout the estrous cycle and early days of pregnancy, but upregulated on P18 and P22. PTGS2 expression was increased on EL, but it was suppressed by pregnancy on P15, P18, and P22. PTGFS expression was upregulated in both cyclic and pregnant mares compared to d0 and its level was the highest on LD. PTGFR expression was transiently increased on LD and EL and was suppressed during early pregnancy. Both PTGES and PTGER2 expressions were increased on LD, EL, and early pregnancy, but were decreased after the luteolysis in cyclic mares as they remained high on P18 and P22. PTGER4 expression did not change throughout the cycle and early pregnancy. Levels of HPGD and SLCO2A1 were significantly increased only on P22. In conclusion, PTGS2 expression increases around the time of luteolysis and concurrent upregulation of PTGFS and PTGES indicates that equine endometrium has increased capability of PTG production around the time of luteolysis. However, pregnancy reduces PTGS2 expression, but maintains the high levels of PTGES during early pregnancy along with PTGER2 while PTGFR expression was suppressed. These findings suggest that possible luteotrophic action of PGE₂ is required in early equine pregnancy. PTGS1 is only upregulated later in the early pregnancy suggesting that it is not involved in luteolysis, but could be the main PTGS enzyme at this time during early pregnancy. An increase in HPGD and SLCO2A1 levels on P22 indicates a tight regulation of PTG action by pregnancy.
目的是评估参与前列腺素(PG)生物合成的基因的表达,包括前列腺素 H 合酶-1(PTGS1)和 PTGS2、PGF 合酶(PTGFS)和 PGE 合酶(PTGES)、PGF 受体(PTGFR)、PGE 受体(PTGER2 和 PTGER4)、前列腺素转运蛋白(SLCO2A1)和羟前列腺素脱氢酶-15(HPGD)。在发情周期中,在排卵日(d0,n=4)、晚期发情(LD,n=4)、早期黄体溶解(EL,n=4)和黄体溶解后(AL,n=4)从母马中获得子宫内膜活检。通过每日测量血浆孕酮浓度和超声检查来确认周期阶段。在妊娠第 14 天(P14;n=4)、第 15 天(P15,n=4)、第 18 天(P18,n=4)和第 22 天(P22;n=4)也采集了活检。使用实时 RT-PCR 定量相对 mRNA 表达。在归一化数据上拟合混合模型,并采用最小显着差异检验(α=0.05)。PTGS1 mRNA 的表达在发情周期和妊娠早期均较低,但在 P18 和 P22 时上调。PTGS2 的表达在 EL 时增加,但在 P15、P18 和 P22 时受妊娠抑制。PGF 合酶在循环和妊娠母马中的表达均高于 d0,并且在 LD 时水平最高。PGFR 的表达在 LD 和 EL 时短暂增加,并在妊娠早期受到抑制。PTGES 和 PTGER2 的表达在 LD、EL 和妊娠早期均增加,但在循环母马黄体溶解后降低,因为它们在 P18 和 P22 时仍保持高水平。PTGER4 的表达在整个周期和妊娠早期都没有变化。HPGD 和 SLCO2A1 的水平仅在 P22 时显著增加。总之,PTGS2 的表达在黄体溶解时增加,同时 PGFS 和 PTGES 的上调表明,在黄体溶解时,马的子宫内膜具有增加的 PG 产生能力。然而,妊娠降低了 PTGS2 的表达,但在妊娠早期维持高水平的 PTGES,同时 PTGER2 受到抑制,PGFR 的表达受到抑制。这些发现表明,PGE₂的可能黄体营养作用在早期马妊娠中是必需的。PTGS1 仅在妊娠早期后期上调,这表明它不参与黄体溶解,但可能是此时妊娠早期的主要 PTGS 酶。PG 作用的紧密调节。