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Effect of propofol on prostaglandin E2 production and prostaglandin synthase-2 and cyclooxygenase-2 expressions in amniotic membrane cells

机译:异丙酚对羊膜细胞中前列腺素E2产生及前列腺素合成酶2和环氧合酶-2表达的影响

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Purpose: Surgery during pregnancy can be a cause of preterm labor or birth, possibly resulting from anesthetic agents or direct effects of surgery. This study was aimed to investigate the effect of propofol on uterine contractility by examining prostaglandin E2 (PGE2) production and the expression of PGE synthase 2 (PGES2) and cyclooxygenase-2 (COX-2) in amniotic membrane cells.Methods: Amniotic membranes were collected from healthy full-term women who underwent cesarean section at 37–40 weeks of gestation. The amniotic cells were cultured in α-modified-Eagle’s medium with 10 % fetal bovine serum for 24 h at 5 % CO2 in a 37 °C incubator. Then, various doses of propofol (0.01–10 μg/ml) were used for treatment for 3 h. PGE2 concentrations in conditioned media were evaluated using ELISA. PGES2 and COX-2 expression were examined using RT-PCR and Western blot. Cell viability and apoptosis were examined by MTT, ATP assays, and the TUNEL method.Results: PGE2 production significantly decreased at 0.1 and 1.0 μg/ml propofol concentrations compared to controls. COX-2 and PGES2 mRNA expression was decreased in a dose-dependent manner with a significant difference at 0.1 μg/ml propofol compared to controls. The protein expression of COX-2 showed a similar result to mRNA expression, but protein expression of PGES2 was not significantly decreased. No effect of propofol was found in cell viability.Conclusions: This study showed that propofol reduced the production of PGE2 and the expression of COX-2 and PGES2 without affecting cell viability.
机译:目的:怀孕期间的手术可能是早产或分娩的原因,可能是由于麻醉剂或手术的直接作用引起的。本研究旨在通过检查羊膜细胞中前列腺素E2(PGE2)的产生以及PGE合酶2(PGES2)和环氧合酶2(COX-2)的表达来研究异丙酚对子宫收缩的影响。收集自健康的足月妇女,这些妇女在妊娠37-40周时进行了剖宫产。在含10%胎牛血清的α-修饰的鹰氏培养基中,将羊膜细胞在37°C的培养箱中于5%的二氧化碳中培养24小时。然后,使用各种剂量的异丙酚(0.01-10μg/ ml)治疗3小时。使用ELISA评估条件培养基中PGE2的浓度。使用RT-PCR和Western blot检测PGES2和COX-2的表达。通过MTT法,ATP法和TUNEL法检测细胞活力和凋亡。结果:与对照组相比,丙泊酚浓度为0.1和1.0μg/ ml时,PGE2产生显着降低。与对照组相比,COX-2和PGES2 mRNA表达以剂量依赖性方式降低,丙泊酚的浓度为0.1μg/ ml。 COX-2的蛋白表达显示出与mRNA表达相似的结果,但PGES2的蛋白表达并未显着降低。结论:异丙酚在不影响细胞活力的情况下,降低了PGE2的产生以及COX-2和PGES2的表达。

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