Protective effects of L-arabinose in high-carbohydrate, high-fat diet-induced metabolic syndrome in rats

被引:51
作者
Hao, Lei [1 ]
Lu, Xiaoling [1 ]
Sun, Min [1 ]
Li, Kai [1 ]
Shen, Lingmin [1 ]
Wu, Tao [1 ]
机构
[1] Tianjin Univ Sci & Technol, Coll Food Engn & Biotechnol, Minist Educ, Key Lab Food Nutr & Safety, Tianjin 300457, Peoples R China
关键词
L-Arabinose; metabolic syndrome; hypertension; insulin resistance; adipocytokines; INTESTINAL SUCRASE ACTIVITY; SUCROSE INGESTION; OBESITY; STEATOHEPATITIS; EXPRESSION; STRESS; MODEL;
D O I
10.3402/fnr.v59.28886
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Background: L-Arabinose is a non-caloric sugar, which could affect glucose and lipid metabolism and suppress obesity. However, few reports have described the effect of L-arabinose in metabolic syndrome, a combination of medical disorders that increase the risk of diabetes and cardiovascular disease. Objective: This study was conducted to explore the effects of L-arabinose in rats with metabolic syndrome induced by a high-carbohydrate, high-fat ( HCHF) diet. Methods: After the rat model for metabolic syndrome was successfully established, L-arabinose was administrated by oral gavage for 6 weeks. The biochemical index and histological analysis were measured, and the expression levels of genes related to fatty acid metabolism were analyzed using real-time PCR. Results: Following treatment with L-arabinose, metabolic syndrome rats had an obvious reduction in body weight, systolic blood pressure, diastolic blood pressure, fasting blood glucose, triglycerides, total cholesterol, serum insulin, TNF-alpha, and leptin. Further study showed that treatment with L-arabinose significantly increased the expression of mRNA for hepatic CPT-1 alpha and PDK4, but the expression of mRNA for hepatic ACC alpha was reduced. Conclusions: This work suggests that L-arabinose could lower body weight, Lee's index, and visceral index and improve dyslipidemia, insulin resistance, inflammation, and viscera function, which indicate that it might be a promising candidate for therapies combating metabolic syndrome.
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页数:10
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