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  • 标题:Effects of triacylglycerol and diacylglycerol oils on blood clearance, tissue uptake, and hepatic apolipoprotein B secretion in mice
  • 本地全文:下载
  • 作者:Yasunaga, Koichi ; Saito, Shinichiro ; Zhang, Yuan-Li
  • 期刊名称:JLR Papers In Press
  • 印刷版ISSN:0022-2275
  • 电子版ISSN:1539-7262
  • 出版年度:2007
  • 卷号:48
  • 期号:5
  • 页码:1108-1121
  • DOI:10.1194/jlr.M600524-JLR200
  • 出版社:American Society for Biochemistry and Molecular Biology
  • 摘要:Prior studies have suggested that FAs liberated in the small intestine from ingested 1,3-diacylglycerol (DAG) are inefficiently incorporated into triglyceride (TG) in enterocytes, with less chylomicron TG entering the circulation postprandially. We found less TG, but more monacylglyerol and DAG, with similar total acylglycerol in newly secreted chylomicrons after oral DAG or triacylglycerol (TAG). However, clearance of DAG-chylomicrons was more rapid than that of TAG-chylomicrons; this was associated with more efficient in vitro LPL-mediated lipolysis of DAG-derived chylomicrons. Intravenously infused DAG was also cleared faster than TAG in normal mice, via both LPL-mediated lipolysis and apolipoprotein E (apoE)-dependent hepatic uptake. Infusions of TAG, but not DAG, increased plasma TG levels. Greater delivery of DAG-derived FA to the liver during infusion of DAG led to greater TG secretion versus TAG; this allowed the maintenance of similar hepatic TG levels after DAG and TAG infusions. Of note, apoB secretion was similar after DAG versus TAG, indicating the assembly of larger very low density lipoproteins after DAG. In conclusion, reduced plasma TG levels, after oral or intravenous DAG, result from more efficient clearance of DAG by both LPL lipolysis and apoE-mediated hepatic endocytosis. DAG emulsions may by useful for intravenous nutrition in people with preexisting hypertriglyceridemia. Supplementary key words triglycerides • lipoprotein metabolism • chylomicron metabolism Abbreviations: AG, acylglycerol; AOX, acyl-coenzyme A oxidase; apoB, apolipoprotein B; CE, cholesteryl ester; CEt, cholesterol oleoyl ether; CPT-1, carnitine palmitoyltransferase-1; DAG, diacylglycerol; DO, diolein; MAG, 1-monoacylglycerol; PhP, postheparinized plasma; PPAR{alpha}, peroxisome proliferator-activated receptor {alpha}; TAG, triacylglycerol; TG, triglyceride; TO, triolein
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