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伏马菌素B1的细胞毒性:脂质过氧化以及蛋白质与DNA合成抑制的影响

Cytotoxicity of fumonisin B1: implication of lipid peroxidation and inhibition of protein and DNA syntheses.

作者信息

Abado-Becognee K, Mobio T A, Ennamany R, Fleurat-Lessard F, Shier W T, Badria F, Creppy E E

机构信息

Laboratory of Toxicology and Applied Hygiene, Faculty of Pharmaceutical Sciences, University of Bordeaux 2, France.

出版信息

Arch Toxicol. 1998 Mar;72(4):233-6. doi: 10.1007/s002040050494.

Abstract

The effects of fumonisin B1 (FB1) from Fusarium moniliforme on lipid peroxidation and protein and DNA syntheses were studied in monkey kidney cells (Vero cells). FB1 was found to be a potent inducer of malondialdehyde (MDA), one of the secondary products formed during lipid peroxidation. At 0.14 microM (0.1 microg/ml), FB1 induced 0.496 +/- 0.1 nmoles of MDA/ mg protein, compared to the control level 0.134 +/- 0.01 nmoles of MDA/mg protein (P < 0.005). No inhibition of protein or DNA synthesis was observed at this concentration of FB1. Inhibition of protein and DNA syntheses was observed at FB1 concentrations > 14 microM (10 microg/ml) with an IC50 of 33 microM for both protein synthesis and DNA synthesis. These results indicate that lipid peroxidation is a very sensitive cellular response to the mycotoxin fumonisin B1 observed at concentrations lower than that required to inhibit cellular synthesis of macromolecules, protein and DNA. This oxidative damage induced by FB1 concentrations encountered in naturally contaminated foodstuffs and feed might lead to mutagenicity and genotoxicity.

摘要

研究了来自串珠镰刀菌的伏马菌素B1(FB1)对猴肾细胞(Vero细胞)脂质过氧化以及蛋白质和DNA合成的影响。发现FB1是脂质过氧化过程中形成的次级产物之一丙二醛(MDA)的强效诱导剂。在0.14微摩尔(0.1微克/毫升)时,FB1诱导产生0.496±0.1纳摩尔丙二醛/毫克蛋白质,而对照水平为0.134±0.01纳摩尔丙二醛/毫克蛋白质(P<0.005)。在此FB1浓度下未观察到蛋白质或DNA合成受到抑制。当FB1浓度>14微摩尔(10微克/毫升)时,观察到蛋白质和DNA合成受到抑制,蛋白质合成和DNA合成的半数抑制浓度(IC50)均为33微摩尔。这些结果表明,脂质过氧化是细胞对霉菌毒素伏马菌素B1非常敏感的反应,在低于抑制细胞大分子、蛋白质和DNA合成所需的浓度下即可观察到。天然污染食品和饲料中遇到的FB1浓度所诱导的这种氧化损伤可能会导致致突变性和遗传毒性。

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