Vagnoni K E, Abbruzzese S B, Christiansen N D, Holyoak G R
Department of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan 84322, USA.
J Anim Sci. 2001 Feb;79(2):463-9. doi: 10.2527/2001.792463x.
The effect of lipopolysaccharide on ovine endometrial tissue was examined at estrus (follicular phase) and during the luteal phase. Endometrial tissues were cultured with 0, 1, or 10 microg/mL lipopolysaccharide. After 24 h, culture supernates were harvested and analyzed for PGF2alpha, PGE2, 6-keto-PGF1alpha, thromboxane B2 (TXB2), and cysteinyl-leukotrienes (leukotrienes) using EIA. Homogenates of endometrial tissue were analyzed for prostaglandin endoperoxidase-1 (PTGS-1), and -2 (PTGS-2) as well as Type-I, -II, and -III nitric oxide synthase (NOS) by Western analysis. Follicular phase tissue produced more PGF2alpha (P < 0.001), TXB2 (P < 0.001), and leukotrienes (P < 0.02) than luteal tissue. Lipopolysaccharide increased PGE2 (P < 0.001) and TXB2 (P < 0.02) production by endometrial tissue. Elevations in these eicosanoids were likely due to the measured increases in PTGS-2 (P = 0.002) because no changes in PTGS-1 (P = 0.54) or Type-I, -II, or -III NOS (P > or = 0.20) occurred in endometrial tissue following lipopolysaccharide exposure. These data suggest that the phase of the estrous cycle regulates prostaglandin production by immune-challenged endometrial tissue.
在发情期(卵泡期)和黄体期检测了脂多糖对绵羊子宫内膜组织的影响。将子宫内膜组织与0、1或10微克/毫升的脂多糖一起培养。24小时后,收集培养上清液,并用酶免疫分析(EIA)检测前列腺素F2α(PGF2α)、前列腺素E2(PGE2)、6-酮-前列腺素F1α(6-keto-PGF1α)、血栓素B2(TXB2)和半胱氨酰白三烯(白三烯)。通过蛋白质免疫印迹分析检测子宫内膜组织匀浆中的前列腺素内过氧化物酶-1(PTGS-1)、-2(PTGS-2)以及一氧化氮合酶(NOS)的I型、II型和III型。卵泡期组织比黄体期组织产生更多的PGF2α(P < 0.001)、TXB2(P < 0.001)和白三烯(P < 0.02)。脂多糖增加了子宫内膜组织中PGE2(P < 0.001)和TXB2(P < 0.02)的产生。这些类花生酸的升高可能是由于PTGS-2的测定增加(P = 0.002),因为在脂多糖暴露后子宫内膜组织中PTGS-1(P = 0.54)或I型、II型或III型NOS(P≥0.20)没有变化。这些数据表明发情周期的阶段调节了免疫刺激的子宫内膜组织中前列腺素的产生。