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1,2-萘醌能刺激模型膜中的脂质过氧化作用和胆固醇域形成。

1,2-naphthoquinone stimulates lipid peroxidation and cholesterol domain formation in model membranes.

机构信息

Elucida Research LLC, Beverly, Massachusetts.

出版信息

Invest Ophthalmol Vis Sci. 2013 Nov 1;54(12):7189-97. doi: 10.1167/iovs.13-12793.

Abstract

PURPOSE

Naphthalene induces cataract formation through the accumulation of its reactive metabolite, 1,2-naphthoquinone (1,2-NQ), in the ocular lens. 1,2-NQ increases lens protein oxidation and disrupts fiber cell membrane function; however, the association of these effects with changes in membrane structure is not understood. The goal of this study was to determine the direct effects of 1,2-NQ on membrane lipid oxidation and structural organization.

METHODS

Iodometric approaches were used to measure the effects of naphthalene and 1,2-NQ on lipid hydroperoxide (LOOH) formation in model membranes composed of cholesterol and dilinoleoylphosphatidylcholine. Membrane samples were prepared at various cholesterol-to-phospholipid mole ratios and subjected to autoxidation at 37°C for 48 hours in the absence or presence of either agent alone (0.1-5.0 μM) or in combination with vitamin E. Small-angle x-ray diffraction was used to measure the effects of naphthalene and 1,2-NQ on membrane structure before and after exposure to oxidative stress.

RESULTS

1,2-NQ increased LOOH formation by 250% (P < 0.001) and 350% (P < 0.001) at 1.0 and 5.0 μM, respectively, whereas naphthalene decreased LOOH levels by 25% (P < 0.01) and 10% (NS). The pro-oxidant effect of 1,2-NQ was inversely affected by membrane cholesterol enrichment and completely blocked by vitamin E. 1,2-NQ also increased cholesterol domain formation by 360% in membranes exposed to oxidative stress; however, no significant changes in membrane lipid organization were observed with naphthalene under the same conditions.

CONCLUSIONS

These data suggest a novel mechanism for naphthalene-induced cataract, facilitated by the direct effects of 1,2-NQ on lipid peroxidation and cholesterol domain formation.

摘要

目的

萘通过在眼晶状体中积累其反应性代谢物 1,2-萘醌(1,2-NQ),诱导白内障形成。1,2-NQ 增加晶状体蛋白氧化并破坏纤维细胞膜功能;然而,这些效应与膜结构变化的关联尚不清楚。本研究的目的是确定 1,2-NQ 对膜脂氧化和结构组织的直接影响。

方法

采用碘量法测定萘和 1,2-NQ 对胆固醇和二亚油酰基磷脂酰胆碱组成的模型膜中脂质氢过氧化物(LOOH)形成的影响。在不存在或存在单独的一种试剂(0.1-5.0 μM)或与维生素 E 联合存在的情况下,将膜样品在不同的胆固醇-磷脂摩尔比下制备,并在 37°C 下进行 48 小时的自氧化。采用小角 X 射线衍射法测量萘和 1,2-NQ 在暴露于氧化应激前后对膜结构的影响。

结果

1,2-NQ 在 1.0 和 5.0 μM 时分别使 LOOH 形成增加 250%(P < 0.001)和 350%(P < 0.001),而萘使 LOOH 水平降低 25%(P < 0.01)和 10%(NS)。1,2-NQ 的促氧化作用受到膜胆固醇富集的反向影响,并被维生素 E 完全阻断。1,2-NQ 还使暴露于氧化应激的膜中胆固醇域形成增加 360%;然而,在相同条件下,萘对膜脂组织没有明显影响。

结论

这些数据表明,1,2-NQ 对脂质过氧化和胆固醇域形成的直接作用促进了萘诱导白内障的新机制。

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