首页> 外文期刊>International Journal of Molecular Sciences >Protective Effects of α-Tocopherol, γ-Tocopherol and Oleic Acid, Three Compounds of Olive Oils, and No Effect of Trolox, on 7-Ketocholesterol-Induced Mitochondrial and Peroxisomal Dysfunction in Microglial BV-2 Cells
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Protective Effects of α-Tocopherol, γ-Tocopherol and Oleic Acid, Three Compounds of Olive Oils, and No Effect of Trolox, on 7-Ketocholesterol-Induced Mitochondrial and Peroxisomal Dysfunction in Microglial BV-2 Cells

机译:α-生育酚,γ-生育酚和油酸,三种橄榄油的保护作用以及Trolox对7-胆固醇诱导的小胶质BV-2细胞线粒体和过氧化物酶体功能障碍的保护作用

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Lipid peroxidation products, such as 7-ketocholesterol (7KC), may be increased in the body fluids and tissues of patients with neurodegenerative diseases and trigger microglial dysfunction involved in neurodegeneration. It is therefore important to identify synthetic and natural molecules able to impair the toxic effects of 7KC. We determined the impact of 7KC on murine microglial BV-2 cells, especially its ability to trigger mitochondrial and peroxisomal dysfunction, and evaluated the protective effects of α- and γ-tocopherol, Trolox, and oleic acid (OA). Multiple complementary chemical assays, flow cytometric and biochemical methods were used to evaluate the antioxidant and cytoprotective properties of these molecules. According to various complementary assays to estimate antioxidant activity, only α-, and γ-tocopherol, and Trolox had antioxidant properties. However, only α-tocopherol, γ-tocopherol and OA were able to impair 7KC-induced loss of mitochondrial transmembrane potential, which is associated with increased permeability to propidium iodide, an indicator of cell death. In addition, α-and γ-tocopherol, and OA were able to prevent the decrease in Abcd3 protein levels, which allows the measurement of peroxisomal mass, and in mRNA levels of Abcd1 and Abcd2, which encode for two transporters involved in peroxisomal β-oxidation. Thus, 7KC-induced side effects are associated with mitochondrial and peroxisomal dysfunction which can be inversed by natural compounds, thus supporting the hypothesis that the composition of the diet can act on the function of organelles involved in neurodegenerative diseases.
机译:脂质过氧化产物,例如7-酮胆固醇(7KC),在神经退行性疾病患者的体液和组织中可能会增加,并引发与神经变性相关的小胶质细胞功能障碍。因此,重要的是要确定能够削弱7KC毒性作用的合成和天然分子。我们确定了7KC对小鼠小胶质BV-2细胞的影响,尤其是其触发线粒体和过氧化物酶体功能障碍的能力,并评估了α-和γ-生育酚,Trolox和油酸(OA)的保护作用。多种互补的化学分析,流式细胞仪和生物化学方法被用来评估这些分子的抗氧化和细胞保护特性。根据各种辅助测定法估计抗氧化剂的活性,只有α-和γ-生育酚以及Trolox具有抗氧化特性。但是,只有α-生育酚,γ-生育酚和OA能够损害7KC诱导的线粒体跨膜电位的丧失,这与碘化丙啶的渗透性增加有关,碘化丙啶是细胞死亡的指标。此外,α-和γ-生育酚以及OA能够阻止Abcd3蛋白水平的下降,从而可以测量过氧化物酶体的质量,以及Abcd1和Abcd2的mRNA水平,其编码涉及过氧化物酶体β-的两个转运蛋白。氧化。因此,7KC诱导的副作用与天然化合物可以逆转的线粒体和过氧化物酶体功能障碍有关,从而支持了饮食成分可以作用于涉及神经退行性疾病的细胞器功能的假说。

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