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本文引用的文献

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Temporal pattern of de novo lipogenesis in the postprandial state in healthy men.健康男性餐后状态下从头脂肪生成的时间模式。
Am J Clin Nutr. 2005 Jan;81(1):35-42. doi: 10.1093/ajcn/81.1.35.
2
Investigation of in vivo fatty acid metabolism in AFABP/aP2(-/-) mice.AFABP/aP2基因敲除小鼠体内脂肪酸代谢的研究。
Am J Physiol Endocrinol Metab. 2005 Jan;288(1):E187-93. doi: 10.1152/ajpendo.00256.2004. Epub 2004 Sep 14.
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Increased lipogenesis and fatty acid reesterification contribute to hepatic triacylglycerol stores in hyperlipidemic Txnip-/- mice.脂肪生成增加和脂肪酸再酯化作用导致高脂血症的Txnip基因敲除小鼠肝脏三酰甘油蓄积。
J Nutr. 2004 Jun;134(6):1475-80. doi: 10.1093/jn/134.6.1475.
4
Systemic and forearm triglyceride metabolism: fate of lipoprotein lipase-generated glycerol and free fatty acids.全身及前臂甘油三酯代谢:脂蛋白脂肪酶产生的甘油和游离脂肪酸的去向
Diabetes. 2004 Mar;53(3):521-7. doi: 10.2337/diabetes.53.3.521.
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Hepatic catabolism of remnant lipoproteins: where the action is.残余脂蛋白的肝脏分解代谢:作用所在之处。
Arterioscler Thromb Vasc Biol. 2004 Feb;24(2):213-5. doi: 10.1161/01.ATV.0000115382.53810.24.
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A pilot study of pioglitazone treatment for nonalcoholic steatohepatitis.吡格列酮治疗非酒精性脂肪性肝炎的一项初步研究。
Hepatology. 2004 Jan;39(1):188-96. doi: 10.1002/hep.20012.
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Contribution of hepatic de novo lipogenesis and reesterification of plasma non esterified fatty acids to plasma triglyceride synthesis during non-alcoholic fatty liver disease.非酒精性脂肪性肝病期间肝脏从头脂肪生成及血浆非酯化脂肪酸再酯化对血浆甘油三酯合成的贡献
Diabetes Metab. 2003 Nov;29(5):478-85. doi: 10.1016/s1262-3636(07)70061-7.
8
VALIDATION OF AN INCOMPLETELY COUPLED TWO-COMPARTMENT NONRECYCLING CATENARY MODEL FOR TURNOVER OF LIVER AND PLASMA TRIGLYCERIDE IN MAN.人体肝脏和血浆甘油三酯周转的不完全耦合双室无再循环链状模型的验证
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Nitrogen, lipid, glycogen and deoxyribonucleic acid content of human liver. The effect of brief starvation and intravenous administration of glucose.人体肝脏的氮、脂质、糖原及脱氧核糖核酸含量。短期饥饿及静脉注射葡萄糖的影响。
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A simple method for the isolation and purification of total lipides from animal tissues.一种从动物组织中分离和纯化总脂质的简单方法。
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非酒精性脂肪性肝病患者肝脏中储存并通过脂蛋白分泌的脂肪酸来源。

Sources of fatty acids stored in liver and secreted via lipoproteins in patients with nonalcoholic fatty liver disease.

作者信息

Donnelly Kerry L, Smith Coleman I, Schwarzenberg Sarah J, Jessurun Jose, Boldt Mark D, Parks Elizabeth J

机构信息

Department of Food Science and Nutrition, University of Minnesota, Twin Cities, St. Paul, Minnesota, 55108, USA.

出版信息

J Clin Invest. 2005 May;115(5):1343-51. doi: 10.1172/JCI23621.

DOI:10.1172/JCI23621
PMID:15864352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1087172/
Abstract

Nonalcoholic fatty liver disease (NAFLD) is characterized by the accumulation of excess liver triacylglycerol (TAG), inflammation, and liver damage. The goal of the present study was to directly quantify the biological sources of hepatic and plasma lipoprotein TAG in NAFLD. Patients (5 male and 4 female; 44 +/- 10 years of age) scheduled for a medically indicated liver biopsy were infused with and orally fed stable isotopes for 4 days to label and track serum nonesterified fatty acids (NEFAs), dietary fatty acids, and those derived from the de novo lipogenesis (DNL) pathway, present in liver tissue and lipoprotein TAG. Hepatic and lipoprotein TAG fatty acids were analyzed by gas chromatography/mass spectrometry. NAFLD patients were obese, with fasting hypertriglyceridemia and hyperinsulinemia. Of the TAG accounted for in liver, 59.0% +/- 9.9% of TAG arose from NEFAs; 26.1% +/- 6.7%, from DNL; and 14.9% +/- 7.0%, from the diet. The pattern of labeling in VLDL was similar to that in liver, and throughout the 4 days of labeling, the liver demonstrated reciprocal use of adipose and dietary fatty acids. DNL was elevated in the fasting state and demonstrated no diurnal variation. These quantitative metabolic data document that both elevated peripheral fatty acids and DNL contribute to the accumulation of hepatic and lipoprotein fat in NAFLD.

摘要

非酒精性脂肪性肝病(NAFLD)的特征是肝脏中三酰甘油(TAG)过量积累、炎症和肝损伤。本研究的目的是直接量化NAFLD中肝脏和血浆脂蛋白TAG的生物来源。安排进行医学指示性肝活检的患者(5名男性和4名女性;年龄44±10岁)静脉输注并口服稳定同位素4天,以标记和追踪血清非酯化脂肪酸(NEFA)、膳食脂肪酸以及肝脏组织和脂蛋白TAG中存在的从头脂肪生成(DNL)途径衍生的脂肪酸。通过气相色谱/质谱分析肝脏和脂蛋白TAG脂肪酸。NAFLD患者肥胖,伴有空腹高甘油三酯血症和高胰岛素血症。在肝脏中占TAG的比例中,59.0%±9.9%的TAG来自NEFA;26.1%±6.7%来自DNL;14.9%±7.0%来自饮食。极低密度脂蛋白(VLDL)中的标记模式与肝脏中的相似,在整个标记的4天中,肝脏表现出对脂肪和膳食脂肪酸的相互利用。DNL在禁食状态下升高,且无昼夜变化。这些定量代谢数据表明,外周脂肪酸升高和DNL均导致NAFLD中肝脏和脂蛋白脂肪的积累。