Cohn J S, McNamara J R, Cohn S D, Ordovas J M, Schaefer E J
Lipid Metabolism Laboratory, USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111.
J Lipid Res. 1988 Jul;29(7):925-36.
Twenty two subjects (9 males, 13 females) were fed a fat-rich meal (1 g of fat/kg body weight). Triglyceride-rich lipoproteins (TRL) were isolated by ultracentrifugation (d less than 1.006 g/ml) from blood drawn 0, 3, 6, 9, and 12 hr after the meal. Plasma triglyceride increased then decreased postprandially, while plasma apoA-I and apoB concentrations decreased. TRL triglyceride, TRL total protein, and TRL apoB concentrations all increased then decreased after the fat-rich meal. Postprandial rise in plasma triglyceride was significantly correlated with fasting plasma triglyceride levels (r = 0.66, P less than 0.001); postprandial rise in TRL triglyceride was significantly correlated with fasting TRL triglyceride levels (r = 0.58, P less than 0.01); postprandial rise in TRL apoB was not, however, significantly correlated with fasting TRL apoB levels (r = 0.37, N.S.). TRL apolipoproteins were separated by polyacrylamide gradient (4-22.5%) gel electrophoresis and protein bands were scanned in two dimensions with a laser densitometer. Relative postprandial changes in the concentration of the TRL apolipoproteins were determined. TRL apoB-100, apoB-48, apoE, and apoC increased then decreased postprandially. The increase in TRL apoB-100 after the fat-rich meal was confirmed in 8 subjects by direct measurement of apoB-100 with a monoclonal antibody ELISA assay. ApoA-I concentration in TRL was unchanged. Albumin in the TRL fraction was significantly increased 12 hr after the meal. Subjects with a greater magnitude of postprandial triglyceridemia had a greater increase in TRL triglyceride and TRL apoB, but their TRL apoB-100/apoB-48 ratios were not different from subjects with less pronounced triglyceridemia. Assuming that plasma TRL containing apoB-100 are predominantly derived from the liver, our data suggest that triglyceride-rich lipoproteins from both the liver and intestine make a significant contribution to postprandial triglyceridemia.
22名受试者(9名男性,13名女性)进食富含脂肪的餐食(1克脂肪/千克体重)。在餐后0、3、6、9和12小时采集血液,通过超速离心法(密度小于1.006克/毫升)分离富含甘油三酯的脂蛋白(TRL)。餐后血浆甘油三酯先升高后降低,而血浆载脂蛋白A-I和载脂蛋白B浓度降低。富含脂肪的餐食后,TRL甘油三酯、TRL总蛋白和TRL载脂蛋白B浓度均先升高后降低。餐后血浆甘油三酯的升高与空腹血浆甘油三酯水平显著相关(r = 0.66,P < 0.001);餐后TRL甘油三酯的升高与空腹TRL甘油三酯水平显著相关(r = 0.58,P < 0.01);然而,餐后TRL载脂蛋白B的升高与空腹TRL载脂蛋白B水平无显著相关性(r = 0.37,无显著性差异)。通过聚丙烯酰胺梯度(4 - 22.5%)凝胶电泳分离TRL载脂蛋白,并用激光密度计在二维方向扫描蛋白条带。测定TRL载脂蛋白浓度的相对餐后变化。餐后TRL载脂蛋白B-100、载脂蛋白B-48、载脂蛋白E和载脂蛋白C先升高后降低。在8名受试者中,通过用单克隆抗体ELISA法直接测定载脂蛋白B-100,证实了富含脂肪的餐食后TRL载脂蛋白B-100的增加。TRL中的载脂蛋白A-I浓度未改变。餐后12小时,TRL组分中的白蛋白显著增加。餐后甘油三酯血症程度较高的受试者,其TRL甘油三酯和TRL载脂蛋白B的增加幅度更大,但他们的TRL载脂蛋白B-100/载脂蛋白B-48比值与甘油三酯血症较轻的受试者无差异。假设含有载脂蛋白B-100的血浆TRL主要来源于肝脏,我们的数据表明,来自肝脏和肠道的富含甘油三酯的脂蛋白对餐后甘油三酯血症有显著贡献。