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基于乳蛋白的模型食品的结构修饰会影响健康年轻男性的餐后肠道肽释放和饱腹感。

Structure modification of a milk protein-based model food affects postprandial intestinal peptide release and fullness in healthy young men.

机构信息

Department of Clinical Nutrition, Institute of Public Health and Clinical Nutrition, Food and Health Research Centre, University of Eastern Finland, 70211 Kuopio, Finland.

出版信息

Br J Nutr. 2011 Dec;106(12):1890-8. doi: 10.1017/S0007114511002522. Epub 2011 Jun 21.

Abstract

Physico-chemical and textural properties of foods in addition to their chemical composition modify postprandial metabolism and signals from the gastrointestinal tract. Enzymatic cross-linking of protein is a tool to modify food texture and structure without changing nutritional composition. We investigated the effects of structure modification of a milk protein-based model food and the type of milk protein used on postprandial hormonal, metabolic and appetitive responses. Healthy males (n 8) consumed an isoenergetic and isovolumic test product containing either whey protein (Wh, low-viscous liquid), casein (Cas, high-viscous liquid) or Cas protein cross-linked with transglutaminase (Cas-TG, rigid gel) in a randomised order. Blood samples were drawn for plasma glucose, insulin, cholecystokinin (CCK), glucagon-like peptide 1 and peptide YY analysis for 4 h. Appetite was assessed at concomitant time points. Cas and Wh were more potent in lowering postprandial glucose than Cas-TG during the first hour. Insulin concentrations peaked at 30 min, but the peaks were more pronounced for Cas and Wh than for Cas-TG. The increase in CCK was similar for Cas and Wh in the first 15 min, whereas for Cas-TG, the CCK release was significantly lower, but more sustained. The feeling of fullness was stronger after the consumption of Cas-TG than after the consumption of Cas and Wh. The present results suggest that food structure is more effective in modulating the postprandial responses than the type of dairy protein used. Modification of protein-based food structure could thus offer a possible tool for lowering postprandial glucose and insulin concentrations and enhancing postprandial fullness.

摘要

除了化学成分外,食品的物理化学和质地特性还会改变餐后代谢和胃肠道信号。酶交联蛋白质是一种在不改变营养成分的情况下改变食品质地和结构的工具。我们研究了基于乳蛋白的模型食品的结构修饰以及所使用的乳蛋白类型对餐后激素、代谢和食欲反应的影响。健康男性(n=8)以随机顺序摄入含有乳清蛋白(Wh,低粘性液体)、酪蛋白(Cas,高粘性液体)或转谷氨酰胺酶交联酪蛋白(Cas-TG,刚性凝胶)的等能量等容量的测试产品。在 4 小时内抽取血液样本以分析血浆葡萄糖、胰岛素、胆囊收缩素(CCK)、胰高血糖素样肽 1 和肽 YY。同时评估食欲。在最初的 1 小时内,Cas 和 Wh 比 Cas-TG 更能降低餐后血糖。胰岛素浓度在 30 分钟时达到峰值,但 Cas 和 Wh 的峰值比 Cas-TG 更明显。在最初的 15 分钟内,Cas 和 Wh 的 CCK 增加相似,而 Cas-TG 的 CCK 释放明显较低,但持续时间更长。食用 Cas-TG 后饱腹感比食用 Cas 和 Wh 更强。这些结果表明,食品结构比所使用的乳蛋白类型更能有效地调节餐后反应。因此,修饰基于蛋白质的食品结构可以提供一种降低餐后血糖和胰岛素浓度并增强餐后饱腹感的可能方法。

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