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Enzymatically synthesized glycogen reduces lipid accumulation in diet-induced obese rats
Authors:Takashi Furuyashiki  Rui Ogawa  Yoko Nakayama  Kazuhisa Honda  Hiroshi Kamisoyama  Hiroki Takata  Michiko Yasuda  Takashi Kuriki  Hitoshi Ashida
Affiliation:1. Institute of Health Sciences, Ezaki Glico Co, Ltd, Osaka, Japan;2. Department of Agrobioscience, Graduate School of Agricultural Science, Kobe University, Hyogo, Japan;3. Department of Bioresource Science, Graduate School of Agricultural Science, Kobe University, Hyogo, Japan;4. Organization of Advanced Science and Technology, Kobe University, Hyogo, Japan
Abstract:Based on a recent study indicating that enzymatically synthesized glycogen (ESG) possesses a dietary, fiber-like action, we hypothesized that ESG can reduce the risk of obesity. In this study, the antiobesity effects of ESG were investigated in a model of diet-induced obesity. Male Sprague-Dawley rats were divided into 4 groups and fed a normal or high-fat diet, with or without 20% ESG, for 4 weeks. Body weight, food intake, lipid deposition in the white adipose tissues and liver, fecal lipid excretion, and plasma lipid profiles were measured. At week 3, the body fat mass was measured using an x-ray computed tomography system, which showed that ESG significantly suppressed the high-fat diet–induced lipid accumulation. Similar results were observed in the weight of the adipose tissue after the experiment. Moreover, ESG significantly suppressed the lipid accumulation in the liver but increased fecal lipid excretion. The plasma concentrations of triacylglycerol and nonesterified fatty acid were lowered after a high-fat diet, whereas the total bile acid concentration was increased by ESG. However, the hepatic messenger RNA (mRNA) levels of enzymes related to lipid metabolism were not affected by ESG. Conversely, the mRNA levels of long-chain acyl-CoA dehydrogenase and medium-chain acyl-CoA dehydrogenase were up-regulated by ESG in the muscle. These results suggest that the combined effects of increased fecal lipid excretion, increased mRNA levels of enzymes that oxidize fatty acids in the muscle, and increased total bile acid concentration in the plasma mediate the inhibitory effect of ESG on lipid accumulation.
Keywords:ACC, acetyl-CoA carboxylase   ACO, acyl-CoA oxidase   cDNA, complementary DNA   CHL, cholesterol   CPT, carnitine palmitoyltransferase   CT, computed tomography   ESG, enzymatically synthesized glycogen   FAS, fatty acid synthase   HF, high fat   LCAD, long-chain acyl-CoA dehydrogenase   MCAD, medium-chain acyl-CoA dehydrogenase   mRNA, messenger RNA   NEFA, nonesterified fatty acid   PL, phospholipid   PPAR, peroxisome proliferator&ndash  activated receptor   SCFAs, short-chain fatty acids   TBA, total bile acids   TG, triacylglycerol   UCP, uncoupling protein   VLCAD, very-long-chain acyl-CoA dehydrogenase
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