Hata M, Ito T, Ohwada K
Laboratory Animal Center, Yamagata University Faculty of Medicine, 2-2-2 Iida-nishi, Yamagata-shi, Yamagata 990-9585, Japan.
Lab Anim. 2009 Apr;43(2):174-81. doi: 10.1258/la.2008.007004. Epub 2008 Nov 17.
The postprandial hypertriglyceridaemia (PHT) rabbit, developed as a new animal model of metabolic syndrome, is characterized by PHT, central obesity and glucose intolerance. For detailed investigation of lipid metabolism characteristics in PHT rabbit, the plasma levels of apolipoproteins A-I, B, C-II, C-III and E were measured. Movements of apolipoproteins B100 and B48 were investigated using sodium dodecyl sulphate-polyacrylamide gel electrophoresis to determine whether postprandially increased triglyceride is exogenous or endogenous. The level of apolipoproteins A-I, B, C-II and E were increased in PHT rabbit after feeding. Apolipoproteins B100 and B48 were detected in the plasma fraction of d < 1.006 g/mL of the PHT rabbit. The postprandial increase in apolipoprotein B in the PHT rabbit reflects a numerical increase in lipoprotein particles in the blood; the increase in apolipoproteins C-II and E suggests some disturbance in lipoprotein catabolism. Apolipoprotein B48 was detected postprandially in PHT rabbits. These results suggest that delayed catabolism of exogenous lipids caused the retention of chylomicron remnants in the blood. Results also suggest that activities of the lipolytic enzyme lipoprotein lipase and hepatic triglyceride lipase were deficient and that the hepatic uptake of exogenous lipoproteins was delayed in the PHT rabbit. Especially, for examining remnant hyperlipoproteinaemia in humans, PHT rabbit is an excellent animal model for hypertriglyceridaemia research.
餐后高甘油三酯血症(PHT)兔作为一种新的代谢综合征动物模型,其特征为餐后高甘油三酯血症、中心性肥胖和葡萄糖不耐受。为详细研究PHT兔的脂质代谢特征,测定了载脂蛋白A-I、B、C-II、C-III和E的血浆水平。使用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳研究载脂蛋白B100和B48的动态变化,以确定餐后升高的甘油三酯是外源性还是内源性的。喂食后,PHT兔的载脂蛋白A-I、B、C-II和E水平升高。在PHT兔密度<1.006 g/mL的血浆组分中检测到了载脂蛋白B100和B48。PHT兔餐后载脂蛋白B的增加反映了血液中脂蛋白颗粒数量的增加;载脂蛋白C-II和E的增加表明脂蛋白分解代谢存在一些紊乱。在PHT兔餐后检测到了载脂蛋白B48。这些结果表明,外源性脂质分解代谢延迟导致乳糜微粒残留在血液中潴留。结果还表明,PHT兔的脂解酶脂蛋白脂肪酶和肝甘油三酯脂肪酶活性不足,外源性脂蛋白的肝脏摄取延迟。特别是,对于研究人类残留性高脂蛋白血症,PHT兔是高甘油三酯血症研究的优秀动物模型。