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膳食宏量营养素调节大鼠肝线粒体心磷脂的脂肪酸酰基组成。

Dietary macronutrients modulate the fatty acyl composition of rat liver mitochondrial cardiolipins.

机构信息

Department of Neurosurgery, Brigham and Women's Hospital, Department of Surgery, Harvard Medical School, Boston, MA 02115.

出版信息

J Lipid Res. 2013 Oct;54(10):2623-35. doi: 10.1194/jlr.M036285. Epub 2013 May 20.

DOI:10.1194/jlr.M036285
PMID:23690505
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3770076/
Abstract

The interaction of dietary fats and carbohydrates on liver mitochondria were examined in male FBNF1 rats fed 20 different low-fat isocaloric diets. Animal growth rates and mitochondrial respiratory parameters were essentially unaffected, but mass spectrometry-based mitochondrial lipidomics profiling revealed increased levels of cardiolipins (CLs), a family of phospholipids essential for mitochondrial structure and function, in rats fed saturated or trans fat-based diets with a high glycemic index. These mitochondria showed elevated monolysocardiolipins (a CL precursor/product of CL degradation), elevated ratio of trans-phosphocholine (PC) (18:1/18:1) to cis-PC (18:1/18:1) (a marker of thiyl radical stress), and decreased ubiquinone Q9; the latter two of which imply a low-grade mitochondrial redox abnormality. Extended analysis demonstrated: i) dietary fats and, to a lesser extent, carbohydrates induce changes in the relative abundance of specific CL species; ii) fatty acid (FA) incorporation into mature CLs undergoes both positive (>400-fold) and negative (2.5-fold) regulation; and iii) dietary lipid abundance and incorporation of FAs into both the CL pool and specific mature tetra-acyl CLs are inversely related, suggesting previously unobserved compensatory regulation. This study reveals previously unobserved complexity/regulation of the central lipid in mitochondrial metabolism.

摘要

研究人员研究了膳食脂肪和碳水化合物对 FBNF1 雄性大鼠肝脏线粒体的相互作用,这些大鼠喂食了 20 种不同的低脂肪等热量饮食。动物的生长速度和线粒体呼吸参数基本不受影响,但基于质谱的线粒体脂质组学分析显示,在喂食基于饱和脂肪或反式脂肪且血糖指数较高的饮食的大鼠中,磷脂酰甘油(CL)的水平升高,CL 是一种对于线粒体结构和功能至关重要的磷脂家族。这些线粒体显示出升高的单酰基 CL(CL 降解的前体/产物)、升高的反式磷酸胆碱(PC)(18:1/18:1)与顺式 PC(18:1/18:1)的比值(硫自由基应激的标志物)和减少的泛醌 Q9;后两者意味着存在低度的线粒体氧化还原异常。扩展分析表明:i)膳食脂肪,在较小程度上还有碳水化合物,诱导特定 CL 物种相对丰度的变化;ii)脂肪酸(FA)掺入成熟 CL 经历正调节(>400 倍)和负调节(2.5 倍);iii)膳食脂质丰度和 FA 掺入 CL 库和特定成熟四酰基 CL 的比例呈负相关,表明存在以前未观察到的补偿调节。本研究揭示了线粒体代谢中中心脂质的以前未观察到的复杂性/调节。

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