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实验性胰腺移植过程中细胞细胞膜流动性的改变和脂质过氧化。

Altered cellular membrane fluidity levels and lipid peroxidation during experimental pancreas transplantation.

机构信息

Department of Surgery, Gynaecology and Obstetrics, University of Zaragoza, Zaragoza, Spain.

出版信息

J Bioenerg Biomembr. 2012 Oct;44(5):571-7. doi: 10.1007/s10863-012-9459-7. Epub 2012 Jul 25.

Abstract

Although the pathogenesis of ischemia reperfusion (IR) injury is based on complex mechanisms, free radicals play a central role. We evaluated membrane fluidity and lipid peroxidation during pancreas transplantation (PT) performed in 12 pigs (six donors and six recipients). Fluidity was measured by fluorescence spectroscopy, and malondialdehyde (MDA) and 4-hydroxyalkenals (4-HDA) concentrations were used as an index of lipid oxidation. Pancreatic tissues were collected as follows: (A) donor, immediately before vascular clamping; (B) graft, following perfusion lavage with University of Wisconsin preservation fluid; (C) graft, after 16 h of cold ischemia; and (D) recipient, 30 min vascular postreperfusion. Fluidity and MDA and 4-HDA concentrations were similar in cases A, B, and C. However, there was significant membrane rigidity and increased lipid peroxidation after reperfusion (D). These findings suggest that reperfusion exaggerates oxidative damage and may account for the rigidity in the membranes of allografts during PT.

摘要

尽管缺血再灌注(IR)损伤的发病机制基于复杂的机制,但自由基起着核心作用。我们评估了在 12 头猪(6 个供体和 6 个受体)进行的胰腺移植(PT)过程中的膜流动性和脂质过氧化。通过荧光光谱法测量流动性,并且将丙二醛(MDA)和 4-羟基烯醛(4-HDA)浓度用作脂质氧化的指标。收集以下胰腺组织:(A)供体,在血管夹闭之前;(B)移植物,在用威斯康星大学保存液进行灌洗后;(C)移植物,在 16 小时冷缺血后;以及(D)受体,血管再灌注后 30 分钟。在 A、B 和 C 情况下,流动性和 MDA 及 4-HDA 浓度相似。但是,再灌注后膜刚性增加且脂质过氧化增加(D)。这些发现表明,再灌注加重了氧化损伤,这可能是 PT 期间同种异体移植物膜刚性的原因。

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