Effects of Low-Molecular-Weight Fucoidan and High Stability Fucoxanthin on Glucose Homeostasis, Lipid Metabolism, and Liver Function in a Mouse Model of Type II Diabetes

被引:89
作者
Lin, Hong-Ting Victor [1 ,2 ]
Tsou, Yu-Chi [3 ]
Chen, Yu-Ting [3 ]
Lu, Wen-Jung [1 ]
Hwang, Pai-An [3 ]
机构
[1] Natl Taiwan Ocean Univ, Dept Food Sci, 2 Pei Ning Rd, Keelung 202, Taiwan
[2] Natl Taiwan Ocean Univ, Ctr Excellence Oceans, 2 Pei Ning Rd, Keelung 202, Taiwan
[3] Natl Taiwan Ocean Univ, Dept Biosci & Biotechnol, 2 Pei Ning Rd, Keelung 202, Taiwan
关键词
type II diabetes; db/db mice; brown algae; fucoidan; fucoxanthin; glucose homeostasis; lipid metabolism; live function; MESSENGER-RNA EXPRESSION; WHITE ADIPOSE-TISSUE; INSULIN-RESISTANCE; IN-VIVO; HYPOGLYCEMIC ACTIVITY; LAMINARIA-JAPONICA; BLOOD-GLUCOSE; ECKLONIA-CAVA; HYPERGLYCEMIA; RECEPTORS;
D O I
10.3390/md15040113
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The combined effects of low-molecular-weight fucoidan (LMF) and fucoxanthin (Fx) in terms of antihyperglycemic, antihyperlipidemic, and hepatoprotective activities were investigated in a mouse model of type II diabetes. The intake of LMF, Fx, and LMF + Fx lowered the blood sugar and fasting blood sugar levels, and increased serum adiponectin levels. The significant decrease in urinary sugar was only observed in LMF + Fx supplementation. LMF and Fx had ameliorating effects on the hepatic tissue of db/db mice by increasing hepatic glycogen and antioxidative enzymes, and LMF was more effective than Fx at improving hepatic glucose metabolism. As for glucose and lipid metabolism in the adipose tissue, the expression of insulin receptor substrate (IRS)-1, glucose transporter (GLUT), peroxisome proliferator-activated receptor gamma (PPAR gamma), and uncoupling protein (UCP)-1 mRNAs in the adipose tissue of diabetic mice was significantly upregulated by Fx and LMF + Fx, and levels of inflammatory adipocytokines, such as adiponectin, tumor necrosis factor-alpha (TNF-alpha), and interleukin-6 (IL-6), were significantly modulated only by LMF + Fx supplementation. The efficacy of LMF + Fx supplementation on the decrease in urinary sugar and on glucose and lipid metabolism in the white adipose tissue of db/db mice was better than that of Fx or LMF alone, indicating the occurrence of a synergistic effect of LMF and Fx.
引用
收藏
页数:14
相关论文
共 63 条
[41]   Anti-inflammatory effects of fucoidan through inhibition of NF-κB, MAPK and Akt activation in lipopolysaccharide-induced BV2 microglia cells [J].
Park, Hye Young ;
Han, Min Ho ;
Park, Cheol ;
Jin, Cheng-Yun ;
Kim, Gi-Young ;
Choi, Il-Whan ;
Kim, Nam Deuk ;
Nam, Taek-Jeong ;
Kwon, Taeg Kyu ;
Choi, Yung Hyun .
FOOD AND CHEMICAL TOXICOLOGY, 2011, 49 (08) :1745-1752
[42]   Fucoxanthin, a Marine Carotenoid Present in Brown Seaweeds and Diatoms: Metabolism and Bioactivities Relevant to Human Health [J].
Peng, Juan ;
Yuan, Jian-Ping ;
Wu, Chou-Fei ;
Wang, Jiang-Hai .
MARINE DRUGS, 2011, 9 (10) :1806-1828
[43]   Reversal of nonalcoholic hepatic steatosis, hepatic insulin resistance, and hyperglycemia by moderate weight reduction in patients with type 2 diabetes [J].
Petersen, KF ;
Dufour, S ;
Befroy, D ;
Lehrke, M ;
Hendler, RE ;
Shulman, GI .
DIABETES, 2005, 54 (03) :603-608
[44]   Two-dimensional differential gel electrophoresis/analysis of diethylnitrosamine induced rat hepatocellular carcinoma [J].
Qi, Yanting ;
Chen, Xiaona ;
Chan, Chu-yan ;
Li, Dan ;
Yuan, Chonggang ;
Yu, Fei ;
Lin, Marie C. ;
Yew, David T. ;
Kung, Hsiang-Fu ;
Lai, Lihui .
INTERNATIONAL JOURNAL OF CANCER, 2008, 122 (12) :2682-2688
[45]   Guideline Approach to Therapy in Patients With Newly Diagnosed Type 2 Diabetes [J].
Raz, Itamar .
DIABETES CARE, 2013, 36 :S139-S144
[46]   Mitochondrial uncoupling proteins: from mitochondria to the regulation of energy balance [J].
Ricquier, D ;
Bouillaud, F .
JOURNAL OF PHYSIOLOGY-LONDON, 2000, 529 (01) :3-10
[47]   End-stage renal failure in type 2 diabetes:: A medical catastrophe of worldwide dimensions [J].
Ritz, E ;
Rychlík, I ;
Locatelli, F ;
Halimi, S .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1999, 34 (05) :795-808
[48]   GLUCOSE TOXICITY [J].
ROSSETTI, L ;
GIACCARI, A ;
DEFRONZO, RA .
DIABETES CARE, 1990, 13 (06) :610-630
[49]  
SEIFTER S, 1950, ARCH BIOCHEM, V25, P191
[50]  
STAUBER JL, 1988, J PHYCOL, V24, P158