Anti-obesity effect of dietary diacylglycerol in C57BL/6J mice:dietary diacylglycerol stimulates intestinal lipid metabolism

• Published in: Journal of lipid research Vol. 43; no. 8; pp. 1312 - 1319
• Main Authors: Murase, Takatoshi, Aoki, Masafumi, Wakisaka, Takuya, Hase, Tadashi, Tokimitsu, Ichiro
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.08.2002; Elsevier
• Subjects: Animals; Anti-Obesity Agents - administration & dosage; Anti-Obesity Agents - pharmacology; Diglycerides - administration & dosage; Diglycerides - pharmacology; Intestinal Mucosa - metabolism; Intestines - drug effects; Lipid Metabolism; Male; Mice; Mice, Inbred C57BL; obesity; small intestine; triacylglycerol; β-oxidation; β-oxidation; small intestine; triacylglycerol; obesity
• ISSN: 0022-2275; 1539-7262
• DOI: 10.1194/jlr.M200094-JLR200

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 β-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 [14C]DG and those of [14C]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.