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稀有糖,如D-阿洛酮糖、D-塔格糖和D-山梨糖,对大鼠的脂质代谢有不同的调节作用。

Rare sugars, d-allulose, d-tagatose and d-sorbose, differently modulate lipid metabolism in rats.

作者信息

Nagata Yasuo, Mizuta Narumi, Kanasaki Akane, Tanaka Kazunari

机构信息

Department of Nutrition, University of Nagasaki, Siebold, Nagasaki, Japan.

Center for Industry, University and Government Cooperation, Nagasaki University, Nagasaki, Japan.

出版信息

J Sci Food Agric. 2018 Mar;98(5):2020-2026. doi: 10.1002/jsfa.8687. Epub 2017 Nov 3.

Abstract

BACKGROUND

Rare sugars including d-allulose, d-tagatose, and d-sorbose are present in limited quantities in nature; some of these rare sugars are now commercially produced using microbial enzymes. Apart from the anti-obesity and anti-hyperglycaemic activities of d-allulose, effects of these sugars on lipid metabolism have not been investigated. Therefore, we aimed to determine if and how d-tagatose and d-sorbose modulate lipid metabolism in rats. After feeding these rare sugars to rats, parameters on lipid metabolism were determined.

RESULTS

No diet-related effects were observed on body weight and food intake. Hepatic lipogenic enzyme activity was lowered by d-allulose and d-sorbose but increased by d-tagatose. Faecal fatty acid excretion was non-significantly decreased by d-allulose, but significantly increased by d-sorbose without affecting faecal steroid excretion. A trend toward reduced adipose tissue weight was observed in groups fed rare sugars. Serum adiponectin levels were decreased by d-sorbose relative to the control. Gene expression of cholesterol metabolism-related liver proteins tended to be down-regulated by d-allulose and d-sorbose but not by d-tagatose. In the small intestine, SR-B1 mRNA expression was suppressed by d-sorbose.

CONCLUSION

Lipid metabolism in rats varies with rare sugars. Application of rare sugars to functional foods for healthy body weight maintenance requires further studies. © 2017 Society of Chemical Industry.

摘要

背景

包括d-阿洛酮糖、d-塔格糖和d-山梨糖在内的稀有糖在自然界中含量有限;其中一些稀有糖现在通过微生物酶进行商业生产。除了d-阿洛酮糖的抗肥胖和抗高血糖活性外,这些糖对脂质代谢的影响尚未得到研究。因此,我们旨在确定d-塔格糖和d-山梨糖是否以及如何调节大鼠的脂质代谢。在给大鼠喂食这些稀有糖后,测定了脂质代谢参数。

结果

未观察到与饮食相关的体重和食物摄入量变化。d-阿洛酮糖和d-山梨糖降低了肝脏生脂酶活性,但d-塔格糖使其升高。d-阿洛酮糖使粪便脂肪酸排泄量略有下降,d-山梨糖使其显著增加,且不影响粪便类固醇排泄。在喂食稀有糖的组中观察到脂肪组织重量有减轻趋势。与对照组相比,d-山梨糖降低了血清脂联素水平。d-阿洛酮糖和d-山梨糖使胆固醇代谢相关肝脏蛋白的基因表达有下调趋势,但d-塔格糖无此作用。在小肠中,d-山梨糖抑制了SR-B1 mRNA的表达。

结论

大鼠的脂质代谢因稀有糖而异。将稀有糖应用于功能性食品以维持健康体重需要进一步研究。© 2017化学工业协会。

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