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体内肝脏氧化损伤后,线粒体磷脂双分子层结构遭到破坏。

Mitochondrial phospholipid bilayer structure is ruined after liver oxidative injury in vivo.

作者信息

Megli Francesco M, Sabatini Karen

机构信息

Dipartimento di Biochimica e Biologia Molecolare, Università di Bari, Centro di Studio sui Mitocondri e Metabolismo Energetico--CNR, Via E. Orabona, 4-70126 Bari, Italy.

出版信息

FEBS Lett. 2004 Aug 27;573(1-3):68-72. doi: 10.1016/j.febslet.2004.07.057.

Abstract

The purpose of this study was to investigate whether, after oxidative injury in vivo, liver mitochondrial phospholipids suffered from structural defects similar to those we have previously observed after either chemical oxidation or respiration state IV incubation of isolated mitochondria in vitro. Oxidative injury of the liver was simulated by endogastric administration of CCl4 to rats in variable amounts for different times, under various conditions. Measurements of the phospholipid bilayer packing order were carried out by electron paramagnetic resonance (EPR) spectrometry of oriented planar samples of phospholipids extracted from liver mitochondria, spin labeled with 5-doxylstearoyl-lecithin. Disordering of the bilayer was revealed by the anisotropy loss of EPR spectra and reached a maximum value 4.5 h after CCl4 administration, vanishing thereafter. The observed disorder also increased with the amount of CCl4 administered, showing distinct dose-dependence, while administration of resveratrol soon after carbon tetrachloride decreased bilayer disordering by 50%. On the contrary, the order parameter S of spin labeled lecithin in isolated mitochondrial membranes from intoxicated rats revealed no change in membrane fluidity after oxidative stress. It is concluded that the phospholipid damage leading to disturbed bilayer geometry after oxidative attack already observed in model membranes and in isolated mitochondria in vitro also occurs in a simulated pathological state in vivo, indicating its possible occurrence also in real oxidative stress-linked pathologies as a contribution to the onset/sustaining of related diseases.

摘要

本研究的目的是调查在体内发生氧化损伤后,肝线粒体磷脂是否会出现与我们之前在体外对分离的线粒体进行化学氧化或呼吸状态IV孵育后所观察到的类似结构缺陷。在各种条件下,通过向大鼠胃内给予不同剂量的CCl4不同时间来模拟肝脏的氧化损伤。通过电子顺磁共振(EPR)光谱法对从肝线粒体中提取的磷脂定向平面样品进行测量,该样品用5-二氧硬脂酰卵磷脂进行自旋标记,以测量磷脂双层堆积顺序。EPR光谱的各向异性损失揭示了双层的无序状态,在给予CCl4后4.5小时达到最大值,此后消失。观察到的无序状态也随着CCl4给药量的增加而增加,呈现出明显的剂量依赖性,而在四氯化碳给药后不久给予白藜芦醇可使双层无序状态降低50%。相反,来自中毒大鼠的分离线粒体膜中自旋标记卵磷脂的序参数S显示氧化应激后膜流动性没有变化。结论是,在模型膜和体外分离的线粒体中已经观察到氧化攻击后导致双层几何结构紊乱的磷脂损伤在体内模拟病理状态下也会发生,这表明在实际的氧化应激相关病理中也可能发生,对相关疾病的发生/持续有一定作用。

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