Curcuminoids and sesquiterpenoids in turmeric (Curcuma longa L.) suppress an increase in blood glucose level in type 2 diabetic KK-Ay mice

被引:270
作者
Nishiyama, T
Mae, T [1 ]
Kishida, H
Tsukagawa, M
Mimaki, Y
Kuroda, M
Sashida, Y
Takahashi, K
Kawada, T
Nakagawa, K
Kitahara, M
机构
[1] Kaneka Corp, Life Sci RD Ctr, Funct Food Dev Div, Takasago, Hyogo 6768688, Japan
[2] Kaneka Corp, Life Sci RD Ctr, Life Sci Res Labs, Takasago, Hyogo 6768688, Japan
[3] Tokyo Univ Pharm & Life Sci, Sch Pharm, Lab Med Plant Sci, Hachioji, Tokyo 1920392, Japan
[4] Tohoku Univ, Sch Med, Dept Internal Med, Dept Mol Metab & Diabet, Sendai, Miyagi 9808574, Japan
[5] Kyoto Univ, Grad Sch Agr, Div Food Sci & Biotechnol, Lab Mol Funct Food, Kyoto 6110011, Japan
关键词
Curcuma longa L; turmeric extract; curcuminoid; sesquiterpenoid; type; 2; diabetes; KK-A(y) mice; PPAR-gamma ligand;
D O I
10.1021/jf0483873
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Turmeric, the rhizome of Curcuma longa L., has a wide range of effects on human health. The chemistry includes curcuminoids and sesquiterpenoids as components, which are known to have antioxidative, anticarcinogenic, and antiinflammatory activities. In this study, we investigated the effects of three turmeric extracts on blood glucose levels in type 2 diabetic KK-A(y) mice (6 weeks old, n = 5/group). These turmeric extracts were obtained by ethanol extraction (E-ext) to yield both curcuminoids and sesquiterpenoids, hexane extraction (H-ext) to yield sesquiterpenoids, and ethanol extraction from hexane- extraction residue (HE-ext) to yield curcuminoids. The control group was fed a basal diet, while the other groups were fed a diet containing 0.1 or 0.5 g of H-ext or HE-ext/100 g of diet or 0.2 or 1.0 g of E-ext/100 g of diet for 4 weeks. Although blood glucose levels in the control group significantly increased (P < 0.01) after 4 weeks, feeding of 0.2 or 1.0 g of E-ext, 0.5 g of H-ext, and 0.5 g of HE-ext/100 g of diet suppressed the significant increase in blood glucose levels. Furthermore, E-ext stimulated human adipocyte differentiation, and these turmeric extracts had human peroxisome proliferator-activated receptor-gamma (PPAR-gamma) ligand-binding activity in a GAL4-PPAR-gamma chimera assay. Also, curcumin, demethoxycurcumin, bisdemethoxycurcumin, and arturmerone had PPAR-gamma ligand-binding activity. These results indicate that both curcuminoids and sesquiterpenoids in turmeric exhibit hypoglycemic effects via PPAR-gamma activation as one of the mechanisms, and suggest that E-ext including curcuminoids and sesquiterpenoids has the additive or synergistic effects of both components.
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收藏
页码:959 / 963
页数:5
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