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补充脂肪酸可保护肺动脉内皮细胞免受氧化损伤。

Fatty acid supplementation protects pulmonary artery endothelial cells from oxidant injury.

作者信息

Hart C M, Tolson J K, Block E R

机构信息

Department of Medicine, University of Florida College of Medicine, Gainesville.

出版信息

Am J Respir Cell Mol Biol. 1990 Nov;3(5):479-89. doi: 10.1165/ajrcmb/3.5.479.

Abstract

Although supplemental fatty acids have been shown to alter the susceptibility of experimental animals to oxidant gases, the relationship between the degree of tissue fatty acyl unsaturation and resistance to oxidant exposure remains undefined. Because vascular endothelial cells have been demonstrated to be sensitive cellular targets in oxidant-induced lung injury, we evaluated the effects of a supplemental fatty acid on the lipid composition and oxidant susceptibility of pulmonary artery endothelial cells (PAEC) in monolayer culture. PAEC were incubated in culture medium supplemented with an ethanolic solution of 0.1 mM cis-vaccenic acid (CVA), an 18-carbon monounsaturated fatty acid, or with the ethanol vehicle alone for 3 h. Cells were then exposed to either control or oxidant (hyperoxia: 95% O2; or hydrogen peroxide: 100 microM) conditions. Oxidant-induced cell injury was assessed by phase-contrast microscopy and by measuring the release of intracellular lactate dehydrogenase. Incubation with CVA increased the CVA content of PAEC lipids and protected cells from oxidant-induced injury for up to 72 h after supplementation. CVA had no effect on nonoxidant-induced cell injury. Although the mechanism by which CVA protects cells against oxidant injury remains undefined, evidence is presented that indicates the mechanism does not involve induction of antioxidant enzyme activity, alterations in the physical state of PAEC membranes, or enhancement of PAEC nucleic acid repair mechanisms. These results define a useful model for exploring the relationship between lipid composition and oxidant susceptibility and suggest that fatty acid modifications may constitute an important strategy for protecting cells against oxidant injury.

摘要

尽管已表明补充脂肪酸会改变实验动物对氧化气体的易感性,但组织脂肪酸酰基不饱和度程度与抗氧化剂暴露抵抗力之间的关系仍不明确。由于血管内皮细胞已被证明是氧化诱导性肺损伤中敏感的细胞靶点,我们评估了补充脂肪酸对单层培养的肺动脉内皮细胞(PAEC)脂质组成和氧化易感性的影响。将PAEC在补充有0.1 mM顺式vaccenic酸(CVA,一种18碳单不饱和脂肪酸)乙醇溶液的培养基中,或仅在乙醇载体中孵育3小时。然后将细胞暴露于对照或氧化剂(高氧:95% O2;或过氧化氢:100 microM)条件下。通过相差显微镜和测量细胞内乳酸脱氢酶的释放来评估氧化剂诱导的细胞损伤。用CVA孵育增加了PAEC脂质中的CVA含量,并在补充后长达72小时保护细胞免受氧化剂诱导的损伤。CVA对非氧化剂诱导的细胞损伤没有影响。尽管CVA保护细胞免受氧化剂损伤的机制仍不明确,但有证据表明该机制不涉及抗氧化酶活性的诱导、PAEC膜物理状态的改变或PAEC核酸修复机制的增强。这些结果定义了一个用于探索脂质组成与氧化易感性之间关系的有用模型,并表明脂肪酸修饰可能构成保护细胞免受氧化剂损伤的重要策略。

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