Reduced glycaemic and insulinaemic responses following trehalose ingestion: implications for postprandial substrate use

Br J Nutr. 2009 Nov;102(10):1395-9. doi: 10.1017/S000711450999050X. Epub 2009 Aug 7.

Abstract

The proposed impact of slowly digestible sources of dietary carbohydrate in reducing the risk of developing obesity and related metabolic disorders remains unclear. The aim of the present study was to compare the postprandial metabolic response to the ingestion of glucose v. trehalose. We hypothesised that the reduced digestion and absorption rate of trehalose is accompanied by an attenuated glycaemic and insulinaemic response, leading to a less inhibited postprandial fat oxidation rate. In a randomised, single-blind, cross-over study, ten overweight subjects ingested two carbohydrate drinks (75 g carbohydrate equivalents of trehalose or glucose) following an overnight fast (08.40 hours) and together with a standardised mixed meal (12.30 hours; 25 % total energy content was provided as either glucose or trehalose). Blood samples were collected before ingestion and every 30 min thereafter for a period of 3 h; substrate use was assessed by indirect calorimetry and expired breath samples were collected. Ingestion of carbohydrates with a mixed meal resulted in a lower peak glucose response and a lower change in area under the curve (DeltaAUC) following trehalose when compared with glucose. Differences in peak insulin response and DeltaAUC were observed with trehalose when compared with glucose during the morning and afternoon. These differences were accompanied with a reduced carbohydrate oxidation after trehalose when ingested as a drink, whilst no significant differences in fat oxidation between drink were observed.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Blood Glucose / drug effects*
  • Carbohydrate Metabolism
  • Cross-Over Studies
  • Fatty Acids, Nonesterified / blood
  • Female
  • Glucose / pharmacology*
  • Humans
  • Insulin / blood*
  • Lipid Peroxidation
  • Male
  • Oxidation-Reduction
  • Postprandial Period
  • Time Factors
  • Trehalose / pharmacology*
  • Triglycerides / blood

Substances

  • Blood Glucose
  • Fatty Acids, Nonesterified
  • Insulin
  • Triglycerides
  • Trehalose
  • Glucose