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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Prostaglandins modulate nitric oxide synthase activity early in time in the uterus of estrogenized rat challenged with lipopolysaccharide.
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Prostaglandins modulate nitric oxide synthase activity early in time in the uterus of estrogenized rat challenged with lipopolysaccharide.

机译:前列腺素在受脂多糖攻击的雌激素大鼠的子宫中较早地调节一氧化氮合酶活性。

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摘要

The aim of our study was to investigate if the lipopolysaccharide (LPS) differentially modulates throughout time the nitric oxide synthase (NOS) and cyclooxygenase (COX) enzymes in the estrogenized rat uterus. To study the effect of LPS throughout time on nitric oxide and prostaglandins production and on NOS and COX expression in the estrogenized rat uterus, females received 5 mg/kg intraperitoneally (i.p.) of LPS and were sacrificed 0.5, 1, 2, 3, 4 and 5 h post-administration. NO production was measured by arginine-citrulline conversion assay and prostaglandin E2/prostaglandin F2alpha by radioconversion. Enzyme expression was evaluated by Western blot analysis. The present work shows that LPS augmented NOS activity 3 h post-treatment and iNOS expression earlier, 2 h post-administration. On the other hand, the administration of LPS stimulated the production of prostaglandin E2/prostaglandin F2alpha and augmented the expression of COX-I 1 h after the treatment and of COX-II 2 h post-treatment. Meloxicam, a COX-II inhibitor, stimulated NO production in a group of rats injected i.p. with both LPS and the inhibitor and sacrificed 2 h after the treatment. These results indicate that, in the estrogenized rat uterus challenged with LPS, the early stimulation in the production of prostaglandins inhibited NOS activity, until the expression of the NOS isoforms is sufficient to overpass the inhibitory effect of the prostaglandins. The above findings suggest that the interaction between NOS and COX might be important in the regulation of physiopathologic events during pregnancy.
机译:我们研究的目的是研究脂多糖(LPS)是否在整个时间段内对雌激素大鼠子宫中的一氧化氮合酶(NOS)和环氧化酶(COX)进行差异调节。为了研究LPS对雌激素大鼠子宫中一氧化氮和前列腺素生成以及NOS和COX表达的影响,雌性大鼠腹膜内(ip)接受5 mg / kg LPS,并处死0.5、1、2、3、4给药后5小时。通过精氨酸-瓜氨酸转化测定法测量NO产生,通过放射转化测量前列腺素E2 /前列腺素F2α。通过蛋白质印迹分析评估酶的表达。本工作表明,LPS在治疗后3小时和iNOS表达较早(给药后2小时)增强了NOS活性。另一方面,LPS的施用刺激了治疗后1小时和治疗后2小时COX-I的表达,并刺激了前列腺素E2 /前列腺素F2α的产生。美洛昔康(一种COX-II抑制剂)刺激了一组经腹膜内注射的大鼠体内NO的产生。用LPS和抑制剂同时给药,并在治疗后2小时处死。这些结果表明,在LPS激发的雌激素大鼠子宫中,前列腺素生产中的早期刺激抑制了NOS活性,直到NOS同工型的表达足以超过前列腺素的抑制作用。上述发现表明,NOS和COX之间的相互作用可能在调节怀孕期间的生理病理事件中很重要。

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