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首页> 外文期刊>Mechanisms of Ageing and Development >Ageing alters the production of nitric oxide and prostanoids after IL-1beta exposure in mesenteric resistance arteries.
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Ageing alters the production of nitric oxide and prostanoids after IL-1beta exposure in mesenteric resistance arteries.

机译:IL-1β暴露于肠系膜阻力动脉后,老化会改变一氧化氮和前列腺素的产生。

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摘要

We aimed to analyse age influence on the production of inflammatory mediators from inducible isoforms of nitric oxide synthase (iNOS) and cyclooxygenase (COX-2) in rat mesenteric resistance arteries (MRA). The second and/or third branches of MRA from young (3-month-old) and old (22-month-old) male Sprague-Dawley rats were incubated in culture medium with or without interleukin-1ss (IL-1ss; 10 ng/ml, 14 h). IL-1ss did not modify endothelial NOS (eNOS) expression or endothelial cell distribution. However, IL-1ss increased nitrite production and iNOS expression in endothelial and smooth muscle cells more in arteries from young than from old rats. IL-1ss also increased PGI(2) levels and COX-2 expression in the three layers of the vascular wall. Ageing did not affect COX-2 expression but did increase TXA(2) and PGF(2alpha) levels. The maximum contraction to phenylephrine was increased in arteries from old rats after IL-1ss treatment. Inhibition of iNOS and COX-2 with 1400 W and NS398, respectively, abolished the differences in phenylephrine contraction. In conclusion, IL-1ss induced an inflammatory response in MRA with associated increases in iNOS and COX-2 expression. The lower increase in nitrite production from iNOS together with a greater contractile prostanoid production in the old rats would be responsible for the increase observed in their contraction to phenylephrine after IL-1 ss treatment.
机译:我们旨在分析年龄对大鼠肠系膜抵抗性动脉(MRA)中一氧化氮合酶(iNOS)和环氧合酶(COX-2)的可诱导同工型对炎性介质产生的影响。在有或没有白介素1ss(IL-1ss; 10 ng)的培养基中孵育来自年轻(3个月大)和老龄(22个月大)雄性Sprague-Dawley大鼠的MRA的第二和/或第三分支。 / ml,14小时)。 IL-1ss不会改变内皮NOS(eNOS)的表达或内皮细胞的分布。然而,IL-1ss增加了幼鼠动脉中的内皮细胞和平滑肌细胞中亚硝酸盐的生成和iNOS的表达,而不是老年大鼠。 IL-1ss还增加了血管壁三层中的PGI(2)水平和COX-2表达。衰老不会影响COX-2的表达,但会增加TXA(2)和PGF(2alpha)的水平。 IL-1ss处理后,老年大鼠的动脉对苯肾上腺素的最大收缩增加。分别用1400 W和NS398抑制iNOS和COX-2消除了去氧肾上腺素收缩的差异。总之,IL-1ss在MRA中诱导了炎症反应,并伴随iNOS和COX-2表达的增加。 iNOS产生的亚硝酸盐产生的增加量较低,而老年大鼠产生的收缩性前列腺素产生量较大,这是IL-1 ss治疗后观察到的它们向去氧肾上腺素收缩的增加的原因。

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