Robin Marie-Anne, Sauvage Ingrid, Grandperret Thomas, Descatoire Véronique, Pessayre Dominique, Fromenty Bernard
INSERM Unité 481, Faculté de Médecine Xavier Bichat, 16 rue Henri Huchard, 75018 Paris, France.
FEBS Lett. 2005 Dec 19;579(30):6895-902. doi: 10.1016/j.febslet.2005.11.029. Epub 2005 Dec 1.
Enhanced hepatic levels of cytochrome P450 2E1 (CYP2E1) may play a key role in the pathogenesis of some liver diseases because CYP2E1 represents a significant source of reactive oxygen species. Although a large fraction of CYP2E1 is located in the endoplasmic reticulum, CYP2E1 is also present in mitochondria. In this study, we asked whether ethanol, a known inducer of microsomal CYP2E1, could also increase CYP2E1 within mitochondria. Our findings indicated that ethanol increased microsomal and mitochondrial CYP2E1 in cultured rat hepatocytes and in the liver of lean mice. This was associated with decreased levels of glutathione, possibly reflecting increased oxidative stress. In contrast, in leptin-deficient obese mice, ethanol administration did not increase mitochondrial CYP2E1, nor it depleted mitochondrial glutathione, suggesting that leptin deficiency hampers mitochondrial targeting of CYP2E1. Thus, ethanol intoxication increases CYP2E1 not only in the endoplasmic reticulum but also in mitochondria, thus favouring oxidative stress in these compartments.
细胞色素P450 2E1(CYP2E1)在肝脏中的水平升高可能在某些肝脏疾病的发病机制中起关键作用,因为CYP2E1是活性氧的重要来源。尽管大部分CYP2E1位于内质网中,但CYP2E1也存在于线粒体中。在本研究中,我们探究了已知的微粒体CYP2E1诱导剂乙醇是否也能增加线粒体中的CYP2E1。我们的研究结果表明,乙醇可增加培养的大鼠肝细胞和瘦小鼠肝脏中的微粒体和线粒体CYP2E1。这与谷胱甘肽水平降低有关,可能反映了氧化应激增加。相反,在瘦素缺乏的肥胖小鼠中,给予乙醇并未增加线粒体CYP2E1,也未消耗线粒体谷胱甘肽,这表明瘦素缺乏会阻碍CYP2E1定位于线粒体。因此,乙醇中毒不仅会增加内质网中的CYP2E1,还会增加线粒体中的CYP₂E1,从而加剧这些区室中的氧化应激。