INRA UMR 866, Dynamique Musculaire et Métabolisme, 34060, Montpellier, France.
J Bioenerg Biomembr. 2012 Aug;44(4):439-52. doi: 10.1007/s10863-012-9448-x. Epub 2012 Jun 12.
No data are reported on changes in mitochondrial membrane phospholipids in non-alcoholic fatty liver disease. We determined the content of mitochondrial membrane phospholipids from rats with non alcoholic liver steatosis, with a particular attention for cardiolipin (CL) content and its fatty acid composition, and their relation with the activity of the mitochondrial respiratory chain complexes. Different dietary fatty acid patterns leading to steatosis were explored. With high-fat diet, moderate macrosteatosis was observed and the liver mitochondrial phospholipid class distribution and CL fatty acids composition were modified. Indeed, both CL content and its C18:2n-6 content were increased with liver steatosis. Moreover, mitochondrial ATP synthase activity was positively correlated to the total CL content in liver phospholipid and to CL C18:2n-6 content while other complexes activity were negatively correlated to total CL content and/or CL C18:2n-6 content of liver mitochondria. The lard-rich diet increased liver CL synthase gene expression while the fish oil-rich diet increased the (n-3) polyunsaturated fatty acids content in CL. Thus, the diet may be a significant determinant of both the phospholipid class content and the fatty acid composition of liver mitochondrial membrane, and the activities of some of the respiratory chain complex enzymes may be influenced by dietary lipid amount in particular via modification of the CL content and fatty acid composition in phospholipid.
目前尚无关于非酒精性脂肪性肝病中线粒体膜磷脂变化的数据。我们测定了非酒精性肝脂肪变性大鼠的线粒体膜磷脂含量,特别关注了心磷脂(CL)的含量及其脂肪酸组成,以及它们与线粒体呼吸链复合物活性的关系。探讨了导致脂肪变性的不同膳食脂肪酸模式。高脂肪饮食导致中度大脂变,改变了肝线粒体磷脂类分布和 CL 脂肪酸组成。事实上,随着肝脂肪变性,CL 含量及其 C18:2n-6 含量均增加。此外,线粒体 ATP 合酶活性与肝磷脂中总 CL 含量和 CL C18:2n-6 含量呈正相关,而其他复合物的活性与肝线粒体总 CL 含量和/或 CL C18:2n-6 含量呈负相关。富含猪油的饮食增加了肝 CL 合酶基因的表达,而富含鱼油的饮食增加了 CL 中的(n-3)多不饱和脂肪酸含量。因此,饮食可能是肝线粒体膜磷脂类含量和脂肪酸组成的重要决定因素,某些呼吸链复合物酶的活性可能会受到膳食脂质量的影响,特别是通过改变磷脂中的 CL 含量和脂肪酸组成。