Chitosan Reduces Plasma Adipocytokines and Lipid Accumulation in Liver and Adipose Tissues and Ameliorates Insulin Resistance in Diabetic Rats

被引:48
作者
Hsieh, Yu-Lin [1 ]
Yao, Hsien-Tsung [3 ]
Cheng, Ron-Shan [2 ]
Chiang, Meng-Tsan [1 ]
机构
[1] Natl Taiwan Ocean Univ, Dept Food Sci, Keelung 202, Taiwan
[2] Natl Taiwan Ocean Univ, Dept Aquaculture, Keelung 202, Taiwan
[3] China Med Univ, Dept Nutr, Taichung 404, Taiwan
关键词
chitosan; chronic inflammation; diabetic rats; fat accumulation; insulin resistance; GLUCAGON-LIKE PEPTIDE-1; MOLECULAR-WEIGHT CHITOSAN; LIPOPROTEIN-LIPASE; METABOLIC SYNDROME; FOOD-INTAKE; PPAR-ALPHA; LONG-TERM; OBESITY; MICE; DIET;
D O I
10.1089/jmf.2011.1882
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Chitosan is a natural product derived from chitin. To investigate the hypoglycemic and anti-obesity effects of chitosan, male Sprague-Dawley rats were divided into four groups: normal control, diabetic, and diabetic fed 5% or 7% chitosan. Diabetes was induced in rats by injecting streptozotocin/nicotinamide. After 10 weeks of feeding, the elevated plasma glucose, tumor necrosis factor-a, and interleukin-6 and lower adiponetin levels caused by diabetes were effectively reversed by chitosan treatment. In addition, 7% chitosan feeding also elevated plasma glucagon-like peptide-1 levels and lowered the insulin resistance index (homeostasis model assessment) in diabetic rats. Lower adipocyte granular intensities and higher lipolysis rates in adipose tissues were noted in the 7% chitosan group. Moreover, chitosan feeding reduced hepatic triglyceride and cholesterol contents and increased hepatic peroxisomal proliferator-activated receptor a expression in diabetic rats. Our results indicate that long-term administration of chitosan may reduce insulin resistance through suppression of lipid accumulation in liver and adipose tissues and amelioration of chronic inflammation in diabetic rats.
引用
收藏
页码:453 / 460
页数:8
相关论文
共 45 条
[1]   Adipose tissue IL-6 content correlates with resistance to insulin activation of glucose uptake both in vivo and in vitro [J].
Bastard, JP ;
Maachi, M ;
Van Nhieu, JT ;
Jardel, C ;
Bruckert, E ;
Grimaldi, A ;
Robert, JJ ;
Capeau, J ;
Hainque, B .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (05) :2084-2089
[2]   Effect of diet on fat cell size and hormone-sensitive lipase activity [J].
Berger, JJ ;
Barnard, RJ .
JOURNAL OF APPLIED PHYSIOLOGY, 1999, 87 (01) :227-232
[3]   FLOW CYTOMETRIC ANALYSIS OF MATURE ADIPOCYTES [J].
BERNSTEIN, RL ;
HYUN, WC ;
DAVIS, JH ;
FULWYLER, MJ ;
PERSHADSINGH, HA .
CYTOMETRY, 1989, 10 (04) :469-474
[4]   Adiposity and diabetes [J].
Bloomgarden, ZT .
DIABETES CARE, 2002, 25 (12) :2342-2349
[5]   Impact of inulin and oligofructose on gastrointestinal peptides [J].
Delzenne, NM ;
Cani, PD ;
Daubioul, C ;
Neyrinck, AM .
BRITISH JOURNAL OF NUTRITION, 2005, 93 :S157-S161
[6]   The biology of incretin hormones [J].
Drucker, DJ .
CELL METABOLISM, 2006, 3 (03) :153-165
[7]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[8]   Cholesterol reduction by glucomannan and chitosan is mediated by changes in cholesterol absorption and bile acid and fat excretion in rats [J].
Gallaher, CM ;
Munion, J ;
Hesslink, R ;
Wise, J ;
Gallaher, DD .
JOURNAL OF NUTRITION, 2000, 130 (11) :2753-2759
[9]   A glucomannan and chitosan fiber supplement decreases plasma cholesterol and increases cholesterol excretion in overweight normocholesterolemic humans [J].
Gallaher, DD ;
Gallaher, CM ;
Mahurt, GJ ;
Carr, TP ;
Hollingshead, CH ;
Hesslink, R ;
Wise, J .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 2002, 21 (05) :428-433
[10]   PPAR-α-null mice are protected from high-fat diet-induced insulin resistance [J].
Guerre-Millo, M ;
Rouault, C ;
Poulain, P ;
André, J ;
Poitout, V ;
Peters, JM ;
Gonzalez, FJ ;
Fruchart, JC ;
Reach, G ;
Staels, B .
DIABETES, 2001, 50 (12) :2809-2814