Mela D J, Cohen R S, Kris-Etherton P M
Nutrition Program, Pennsylvania State University, University Park 16802.
J Nutr. 1987 Oct;117(10):1655-62. doi: 10.1093/jn/117.10.1655.
Obesity in humans is associated with decreased plasma levels of high density lipoprotein (HDL), but the mechanisms effecting this relationship have not been established. Four treatment groups were used to develop a range of moderate adiposity: rat pups were raised in litters of 4 or 14 and fed from weaning diets of 6 or 24% fat (wt/wt) for 15-17 wk. Lipoproteins from plasma and from a recirculating in situ liver perfusion system were then separated and analyzed, lipoprotein lipase (LPL) activity was assayed in samples of adipose tissue and skeletal muscle and body composition and cholesterol concentrations of various tissues were determined. There was little effect of the diet or litter size treatments on plasma lipids or lipoprotein profiles. Compared to the marked changes in lipid and lipoprotein metabolism that have been observed in severely obese animal models, there was generally little effect of the treatments used to produce this model of moderate diet-induced adiposity. Adiposity was unrelated to plasma total cholesterol and triglycerides. While fatness was positively, although weakly, correlated with plasma levels of several HDL components, including HDL cholesterol, there were no consistent treatment effects on these measures. Plasma HDL levels and adiposity were unrelated to hepatic HDL production or tissue LPL activities. A review of the literature suggests that differences in plasma HDL responses to adiposity in humans and in experimental animals may be due to inherent species differences in lipoprotein metabolism.
人类肥胖与血浆高密度脂蛋白(HDL)水平降低有关,但影响这种关系的机制尚未明确。使用四个治疗组来建立一系列中度肥胖模型:将幼鼠饲养在每窝4只或14只的环境中,并从断奶开始分别喂食脂肪含量为6%或24%(重量/重量)的饮食,持续15 - 17周。然后分离并分析血浆和原位肝脏再循环灌注系统中的脂蛋白,测定脂肪组织和骨骼肌样本中的脂蛋白脂肪酶(LPL)活性,并确定各种组织的身体组成和胆固醇浓度。饮食或窝仔大小处理对血浆脂质或脂蛋白谱几乎没有影响。与在严重肥胖动物模型中观察到的脂质和脂蛋白代谢的显著变化相比,用于产生这种中度饮食诱导肥胖模型的处理通常影响很小。肥胖与血浆总胆固醇和甘油三酯无关。虽然肥胖与包括HDL胆固醇在内的几种HDL成分的血浆水平呈正相关,但相关性较弱,且这些指标没有一致的处理效应。血浆HDL水平和肥胖与肝脏HDL产生或组织LPL活性无关。文献综述表明,人类和实验动物血浆HDL对肥胖的反应差异可能归因于脂蛋白代谢中固有的物种差异。