餐后
NEFA公司
食欲
内科学
胆囊收缩素
内分泌学
摄入
胃排空
胰高血糖素样肽-1
胰岛素
曲线下面积
餐食
交叉研究
化学
组织谷氨酰胺转胺酶
脂类消化
消化(炼金术)
医学
胃
糖尿病
生物化学
2型糖尿病
安慰剂
色谱法
酶
脂肪酶
病理
替代医学
受体
作者
Kristiina R. Juvonen,Adam Macierzanka,Martina E. Lille,David Elliot Laaksonen,Hannu M Mykkänen,LEO K. NISKANEN,Jussi Pihlajamäki,Kari A. Mäkelä,Elizabeth N. Clare Mills,Alan R. Mackie,Paul Malcolm,Karl‐Heinz Herzig,Kaisa S Poutanen,Leila J. Karhunen
标识
DOI:10.1017/s0007114515001737
摘要
The physico-chemical and interfacial properties of fat emulsions influence lipid digestion and may affect postprandial responses. The aim of the present study was to determine the effects of the modification of the interfacial layer of a fat emulsion by cross-linking on postprandial metabolic and appetite responses. A total of fifteen healthy individuals (26.5 (sem 6.9) years and BMI 21.9 (sem 2.0) kg/m2) participated in a cross-over design experiment in which they consumed two isoenergetic (1924 kJ (460 kcal)) and isovolumic (250 g) emulsions stabilised with either sodium caseinate (Cas) or transglutaminase-cross-linked sodium caseinate (Cas-TG) in a randomised order. Blood samples were collected from the individuals at baseline and for 6 h postprandially for the determination of serum TAG and plasma NEFA, cholecystokinin (CCK), glucagon-like peptide 1 (GLP-1), glucose and insulin responses. Appetite was assessed using visual analogue scales. Postprandial TAG and NEFA responses and gastric emptying (GE) rates were comparable between the emulsions. CCK increased more after the ingestion of Cas-TG than after the ingestion of Cas (P< 0.05), while GLP-1 responses did not differ between the two test emulsions. Glucose and insulin profiles were lower after consuming Cas-TG than after consuming Cas (P< 0.05). The overall insulin, glucose and CCK responses, expressed as areas above/under the curve, did not differ significantly between the Cas and Cas-TG meal conditions. Satiety ratings were reduced and hunger, desire to eat and thirst ratings increased more after the ingestion of Cas-TG than after the ingestion of Cas (P< 0.05). The present results suggest that even a subtle structural modification of the interfacial layer of a fat emulsion can alter the early postprandial profiles of glucose, insulin, CCK, appetite and satiety through decreased protein digestion without affecting significantly on GE or overall lipid digestion.
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