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[腹膜感染中低白蛋白血症的分子机制与治疗]

[Molecular mechanism and therapy of hypoalbuminemia in peritoneal infection].

作者信息

Li W, Li J, Gu J

机构信息

Nanjing General Hospital of People's Liberation Army.

出版信息

Zhonghua Wai Ke Za Zhi. 1997 Feb;35(2):100-3.

Abstract

Albumin mRNA expression was studied by the use of reverse transcriptional polymerase chain reaction (RT-PCR) to determine the molecular mechanism in peritoneal infection. Albumin mRNA content markedly decreased. Endotoxin inhibited albumin mRNA expression in vivo probably by stimulating TNF,IL-1, and IL-6 production. Changes of the hormone levels were not the cause of hypoalbuminemia in infection. Reconbined growth hormone and astragalus polysaccharides alleviated inhibition albumin synthesis inhibition increasing albumin serum concentration in rats with peritoneal infection. The results suggested that hypoalbuminemia is associated with endotoxemia during sepsis, which inhibites hepatocytes albumin synthesis probably by stimulating nonparenchymal cells to produce TNF, IL-1, and IL-6.

摘要

通过逆转录聚合酶链反应(RT-PCR)研究白蛋白mRNA表达,以确定腹膜感染的分子机制。白蛋白mRNA含量显著降低。内毒素可能通过刺激TNF、IL-1和IL-6的产生来抑制体内白蛋白mRNA表达。激素水平的变化不是感染时低白蛋白血症的原因。重组生长激素和黄芪多糖可减轻腹膜感染大鼠白蛋白合成的抑制,提高血清白蛋白浓度。结果表明,脓毒症期间低白蛋白血症与内毒素血症有关,内毒素血症可能通过刺激非实质细胞产生TNF、IL-1和IL-6来抑制肝细胞白蛋白合成。

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