van Biervliet J P, Rosseneu M, Bury J, Caster H, Stul M S, Lamote R
Pediatr Res. 1986 Apr;20(4):324-8. doi: 10.1203/00006450-198604000-00009.
In this study the lipid and apoprotein profiles were investigated in newborns at 0, 7, and 30 days of life. The plasma lipoproteins were separated both by ultracentrifugation and gel filtration in order to compare the patterns obtained by the two techniques. At birth, the apo E concentration is comparable to that measured in adults, but its distribution among lipoproteins is significantly different as more than 80% of the plasma apo E belongs to high-density lipoproteins (HDL). At 7 and 30 days the plasma apo E concentrations are close to the values at birth, but a significant redistribution occurs from HDL to very low-density lipoproteins. By analogy with apo B, the plasma apo CIII concentration is low at birth and increases between 0 and 7 days by a factor of about two. Plasma triglycerides increase significantly during the first week of life so that the apo CIII increase is most pronounced in very low-density lipoproteins. These lipoproteins therefore become enriched in apo E, apo CIII and triglycerides between 0 and 7 days. At birth, a distinct HDL fraction, enriched in apo E, apo AII and cholesterol (HDLE), could be detected. To compensate for the low LDL levels, this HDLE fraction might function as an additional source for cholesterol delivery to peripheral tissues via the apo (B, E) receptor. At later age, low-density lipoprotein synthesis is enhanced, apo E is transferred to very low-density lipoproteins, and cholesterol delivery via the HDLE becomes less important.(ABSTRACT TRUNCATED AT 250 WORDS)
在本研究中,对出生0天、7天和30天的新生儿的脂质和载脂蛋白谱进行了调查。通过超速离心和凝胶过滤分离血浆脂蛋白,以比较两种技术获得的模式。出生时,载脂蛋白E浓度与成人测得的浓度相当,但其在脂蛋白中的分布显著不同,因为超过80%的血浆载脂蛋白E属于高密度脂蛋白(HDL)。在7天和30天时,血浆载脂蛋白E浓度接近出生时的值,但发生了从HDL到极低密度脂蛋白的显著重新分布。与载脂蛋白B类似,出生时血浆载脂蛋白CIII浓度较低,在0至7天之间增加约两倍。血浆甘油三酯在生命的第一周显著增加,因此载脂蛋白CIII的增加在极低密度脂蛋白中最为明显。因此,这些脂蛋白在0至7天之间富含载脂蛋白E、载脂蛋白CIII和甘油三酯。出生时,可以检测到一个独特的富含载脂蛋白E、载脂蛋白AII和胆固醇的HDL组分(HDLE)。为了补偿低密度脂蛋白水平较低的情况,这个HDLE组分可能作为通过载脂蛋白(B,E)受体向周围组织输送胆固醇的额外来源。在后期,低密度脂蛋白合成增强,载脂蛋白E转移到极低密度脂蛋白,通过HDLE输送胆固醇变得不那么重要。(摘要截短至250字)