Center for Molecular and Vascular Biology, University of Leuven, Herestraat 49, 3000 Leuven, Belgium.
Cardiovasc Pathol. 2011 Jan-Feb;20(1):44-50. doi: 10.1016/j.carpath.2009.09.002. Epub 2009 Nov 14.
The liver is a key organ in lipid and lipoprotein metabolism. It has been postulated that a small diameter of sinusoidal fenestrae retards clearance of chylomicron remnants, resulting in hypercholesterolemia and atherosclerosis. However, this hypothesis has not been rigorously tested hitherto.
In the current study, we compared plasma levels of proatherogenic lipoproteins and assessed the development of atherosclerosis at distinct locations throughout the arterial tree in heterozygous New Zealand White and Dutch Belt rabbits that are deficient in low-density lipoprotein receptor and with an average fenestrae size of 103 and 124 nm, respectively.
Feeding of a 0.15% cholesterol diet for 4 months resulted in similar total plasma cholesterol levels in New Zealand White (420±20 mg/dl) and Dutch Belt (380±30 mg/dl) rabbits. Following isolation of lipoproteins by ultracentrifugation, no biologically significant differences in very-low-density lipoprotein, intermediate-density lipoprotein, and low-density lipoprotein cholesterol levels were observed between cholesterol-fed New Zealand White and Dutch Belt rabbits. Furthermore, the relative amount of intestinally derived apolipoprotein-B48-containing lipoproteins did not differ significantly between both strains (7.3±0.42% vs. 8.0±0.54%). Atherosclerosis was more pronounced in the thoracic aorta in New Zealand White rabbits than in Dutch Belt rabbits, but the reverse was observed with the abdominal aorta. These topographic differences cannot be explained by circulating lipoprotein levels.
The data presented in this study do not support the hypothesis that the diameter of fenestrae is an important determinant of chylomicron remnant levels, diet-induced hypercholesterolemia, and atherosclerosis in cholesterol-fed rabbits.
肝脏是脂质和脂蛋白代谢的关键器官。有人推测,较小的肝窦窗孔直径会阻碍乳糜微粒残粒的清除,导致高胆固醇血症和动脉粥样硬化。然而,迄今为止,这一假说尚未得到严格检验。
在目前的研究中,我们比较了载脂蛋白致动脉粥样硬化脂蛋白在血浆中的水平,并评估了在载脂蛋白致动脉粥样硬化脂蛋白缺乏低密度脂蛋白受体的杂合新西兰白兔和荷兰带兔的动脉树不同部位动脉粥样硬化的发展情况,这两种兔的肝窦窗孔平均直径分别为 103nm 和 124nm。
4 个月的 0.15%胆固醇饮食喂养导致新西兰白兔(420±20mg/dl)和荷兰带兔(380±30mg/dl)总血浆胆固醇水平相似。通过超速离心分离脂蛋白后,在胆固醇喂养的新西兰白兔和荷兰带兔之间,极低密度脂蛋白、中间密度脂蛋白和低密度脂蛋白胆固醇水平没有生物学上的显著差异。此外,两种品系之间肠源性载脂蛋白 B48 含脂蛋白的相对量差异也不显著(7.3±0.42%比 8.0±0.54%)。在新西兰白兔中,胸主动脉的动脉粥样硬化比荷兰带兔更为明显,但在腹主动脉中则相反。这些拓扑差异不能用循环脂蛋白水平来解释。
本研究提供的数据不支持这样一种假说,即窗孔直径是乳糜微粒残粒水平、饮食诱导的高胆固醇血症和胆固醇喂养兔动脉粥样硬化的一个重要决定因素。