Murase Takatoshi, Aoki Masafumi, Wakisaka Takuya, Hase Tadashi, Tokimitsu Ichiro
Biological Science Laboratories, Kao Corporation, 2606 Akabane, Ichikai-machi, Haga-gun, Tochigi 321-3497, Japan.
J Lipid Res. 2002 Aug;43(8):1312-9.
We examined the long-term effects of dietary diacylglycerol (DG) and triacylglycerol (TG) with similar fatty acid compositions on the development of obesity in C57BL/6J mice. We also analyzed the expression of genes involved in lipid metabolism at an early stage of obesity development in these mice. Compared with mice fed the high-TG diet, mice fed the high-DG diet accumulated significantly less body fat during the 8-month study period. Within the first 10 days, dietary DG stimulated beta-oxidation and lipid metabolism-related gene expression, including acyl-CoA oxidase, medium-chain acyl-CoA dehydrogenase, and uncoupling protein-2 in the small intestine but not in the liver, skeletal muscle, or brown adipose tissue, suggesting the predominant contribution of intestinal lipid metabolism to the effects of DG. Furthermore, analysis of digestion products of [(14)C]DG and those of [(14)C]TG revealed that the radioactivity levels detected in fatty acid, 1-monoacylglycerol, and 1,3-DG in intestinal mucosa were significantly higher after intrajejunal injection of DG rather than TG. Thus, dietary DG reduces body weight gain that accompanies the stimulation of intestinal lipid metabolism, and these effects may be related to the characteristic metabolism of DG in the small intestine.
我们研究了具有相似脂肪酸组成的膳食二酰甘油(DG)和三酰甘油(TG)对C57BL/6J小鼠肥胖症发展的长期影响。我们还分析了这些小鼠在肥胖症发展早期参与脂质代谢的基因表达。与喂食高TG饮食的小鼠相比,喂食高DG饮食的小鼠在8个月的研究期间积累的体脂明显更少。在最初的10天内,膳食DG刺激了小肠中β-氧化和脂质代谢相关基因的表达,包括酰基辅酶A氧化酶、中链酰基辅酶A脱氢酶和解偶联蛋白-2,但在肝脏、骨骼肌或棕色脂肪组织中未出现这种情况,这表明肠道脂质代谢对DG的作用起主要作用。此外,对[(14)C]DG和[(14)C]TG消化产物的分析表明,空肠内注射DG后,在肠黏膜中检测到的脂肪酸、1-单酰甘油和1,3-DG中的放射性水平明显高于注射TG后的水平。因此,膳食DG减少了伴随肠道脂质代谢刺激而出现的体重增加,这些作用可能与DG在小肠中的特殊代谢有关。