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首页> 外文期刊>Physiological Research >Lipoprotein lipase activity determined in vivo is lower in carriers of apolipoprotein A-V gene variants 19W and-1131C
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Lipoprotein lipase activity determined in vivo is lower in carriers of apolipoprotein A-V gene variants 19W and-1131C

机译:载脂蛋白A-V基因变体19W和-1131C的携带者体内确定的脂蛋白脂肪酶活性较低

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The apolipoprotein A-V (apo A-V) plays an important role in regulation of triglyceride (TG) concentration in serum. To better understand how apo A-V affects triglyceridemia and glucoregulation, the lipoprotein lipase (LPL) activity was determined using intravenous fat tolerance test (IVFTT) and oral glucose tolerance test (oGTT) was performed in carriers of apolipoprotein A-V gene (APOAV) variants known to be associated with increased triglyceridemia. Twelve carriers of 19W variant, 16 carriers of -1131C variant, 1 combined heterozygote and 16 control subjects homozygous for wild type variants (19S/-1131T) were selected from a population sample and matched with respect to body mass index and age. The APOAV variants carriers had increased TG, very low density lipoprotein-TG, and apo B concentrations (p < 0.05). The LPL activity evaluated as k(2) rate constant for clearance of Intralipid (R) was 14 % lower in APOAV variants carriers. The depression of nonesterified fatty acids (NEFA) concentration after glucose load was delayed in APOAV variants carriers in spite of the same insulinemia and glycemia. Our results suggest that variants of APOAV combined with increased triglyceridemia are associated with lower LPL activity in vivo and with disturbances of regulation of NEFA concentration after glucose load.
机译:载脂蛋白A-V(apo A-V)在调节血清中甘油三酸酯(TG)浓度中起重要作用。为了更好地了解载脂蛋白AV如何影响甘油三酸酯和葡萄糖调节,使用已知的载脂蛋白AV基因(APOAV)变异体的携带者,通过静脉内脂肪耐受性测试(IVFTT)确定了脂蛋白脂酶(LPL)活性,并进行了口服葡萄糖耐受性测试(oGTT)。与甘油三酯血症增加有关。从人群样本中选择12个19W变异的携带者,16个-1131C变异的携带者,1个组合的杂合子和16个野生型变异纯合的对照受试者(19S / -1131T),并根据体重指数和年龄进行匹配。 APOAV变体携带者的TG升高,脂蛋白-TG的密度非常低,且apo B的浓度较高(p <0.05)。在APOAV变异载体中,以脂蛋白(R)清除率的k(2)速率常数评估的LPL活性低14%。尽管存在相同的胰岛素血症和血糖症,但在APOAV变异载体中,葡萄糖负荷后非酯化脂肪酸(NEFA)浓度的降低被延迟了。我们的结果表明,APOAV变异体与甘油三酯血症增加相关,与体内LPL活性降低以及葡萄糖负荷后NEFA浓度调节受到干扰有关。

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