Reduced intake of carbohydrate prevents the development of obesity and impaired glucose metabolism in ghrelin O-acyltransferase knockout mice

被引:17
|
作者
Kouno, Tetsuya [1 ]
Akiyama, Nobuteru [1 ]
Fujieda, Kumiko [1 ]
Nanchi, Isamu [1 ]
Okuda, Tomohiko [1 ]
Iwasaki, Takanori [1 ]
Oka, Shogo [2 ]
Yukioka, Hideo [1 ]
机构
[1] Shionogi & Co Ltd, Shionogi Pharmaceut Res Ctr, 3-1-1 Futaba Cho, Toyonaka, Osaka 5610825, Japan
[2] Kyoto Univ, Human Hlth Sci, Dept Biol Chem, Sakyo Ku, 53 Kawahara Cho, Kyoto 6068507, Japan
关键词
Ghrelin; Carbohydrate; Body weight; Food intake; PROSPECTIVE COHORT; PEPTIDE; HORMONE; RISK;
D O I
10.1016/j.peptides.2016.11.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A close relationship between acylated-ghrelin and sucrose intake has been reported. However, little has been examined about the physiological action of ghrelin on preference for different types of carbohydrate such as glucose, fructose, and starch. The current study was aimed to investigate the role of acylated-ghrelin in the determinants of the choice of carbohydrates, and pathogenesis of chronic disorders, including obesity and insulin resistance. In a two-bottle-drinking test, ghrelin O-acyltransferase (GOAT) knockout (KO) mice consumed a less amount of glucose and maltodextrin, and almost the same amount of fructose and saccharin solution compared to WT littermates. The increased consumption of glucose and maltodextrin was observed when acylated-ghrelin, but not unacylated-ghrelin, was exogeneously administered in normal C57BL/6J mice, suggesting an association of acylated-ghrelin with glucose-containing carbohydrate intake. When fed a diet rich in maltodextrin, starch and fat for 12 weeks, GOAT KO mice showed less food intake and weight gain, as well as improved glucose tolerance and insulin sensitivity than WT mice. Our data suggests that blockade of GOAT activity may offer a therapeutic option for treatment of obesity and its associated metabolic syndrome by preventing from overconsumption of carbohydrate-rich food. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:145 / 152
页数:8
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