Postprandial Period
Conditions
Keywords
Blackcurrant, Citrus, Polyphenols, Glucose, Postprandial, Metabolism
Brief summary
Large postprandial glucose responses are associated with increased risk of chronic diseases, including diabetes and cardiovascular disease. Our group have previously shown that fruit polyphenol extracts, when consumed immediately before a mixed carbohydrate meal, reduce postprandial glycaemia. The aim of this study is to investigate the effects of a blackcurrant polyphenol extract and citrus polyphenol extract (and their combination), on postprandial glycaemia, insulinaemia and gastrointestinal hormone concentrations following a mixed carbohydrate test meal. It is hypothesised that blackcurrant and citrus extracts alone will inhibit glycaemia compared to placebo, and a combination of the two will have a greater effect.
Detailed description
Intake of carbohydrate-rich foods transiently increases blood glucose levels (known as postprandial glycaemia). Repeated high postprandial glucose responses are evidenced to dysregulate functional proteins, oxidative stress and pancreatic beta cell function; thus increasing the risk of diabetes and cardiovascular disease. Accordingly, meals that elicit a reduced, or more gradual, rise in blood glucose levels are desirable. Fruit polyphenols may help to limit the glucose excursion following a high carbohydrate meal. Previous research by our group has demonstrated that blackcurrant polyphenols significantly inhibited the average incremental area under the curve (T+0 to +30 min) of plasma glucose. Possible mechanisms include inhibition of intestinal enzymes and inhibition of intestinal glucose absorption by decreasing Sodium-glucose linked transporter 1 (SGLT-1) / Glucose transporter 2 (GLUT-2) glucose transporter activity. In vitro data suggests that citrus polyphenols may impact on carbohydrate metabolism by binding to starch molecules, however, effects on postprandial glycaemia are not yet known. Blackcurrants and citrus fruits have distinct polyphenol profiles and may therefore act on glucose homeostasis via different mechanisms. Blackcurrants are rich in anthocyanins and flavanols, whereas citrus fruits are rich in flavanones, hesperetin and naringenin. Theoretically, combining blackcurrant with citrus extracts may have synergistic effects. The aim of this study is to investigate the effects of blackcurrant polyphenol extracts and citrus polyphenol extracts (and their combination), on postprandial glycaemia, insulinaemia and gastrointestinal hormone concentrations following a mixed carbohydrate test meal. It is hypothesised that blackcurrant and citrus extracts alone will inhibit glycaemia compared to placebo, a combination of the two will have a greater effect. Study design: A randomised, controlled, double-blind, cross-over study will be conducted. Subjects will consume different drinks at 4 separate study visits. Drinks will contain either: blackcurrant extract (low dose), blackcurrant extract (high dose), citrus extract (low dose), blackcurrant and citrus extract (low dose + low dose), or placebo (no polyphenols). The study will utilise an incomplete block design. Subjects will consume the placebo drink and 3 out of 4 of the polyphenol-containing drinks during the study. At least a 7-day wash-out period will be required between study days. Baseline (fasted) blood samples will be taken in duplicate at T-10 min and T-5 min before consuming the test drink (T+0 min). Immediately following consumption of the drink, a mixed carbohydrate test meal will be consumed. Further blood samples will be collected at 10 min intervals for the first 30 min and then every 15 min until T+90 min and at T+120 min. Blood samples will be analysed for plasma glucose, insulin, glucose-dependent insulinotropic peptide (GIP), glucagon-like peptide 1 (GLP-1), peptide YY (PYY), C-peptide and nonesterified fatty acids (NEFA).
Interventions
Participants will consume a small beverage that contains blackcurrant extract (low dose) immediately before a high-carbohydrate meal.
Participants will consume a small beverage that contains no fruit extracts immediately before a high-carbohydrate meal.
Participants will consume a small beverage that contains citrus extract (low dose) immediately before a high-carbohydrate meal.
Participants will consume a small beverage that contains blackcurrant extract (high dose) immediately before a high-carbohydrate meal.
Participants will consume a small beverage that contains blackcurrant and citrus extracts (low dose / low dose)immediately before a high-carbohydrate meal.
Sponsors
Study design
Intervention model description
Incomplete block cross-over design. Each participant receives placebo plus 3 out of 4 active treatments.
Eligibility
Inclusion criteria
* Age: 18-70 years * Men and women * Healthy (free of diagnosed diseases listed in the
Exclusion criteria
) * Body Mass Index 18-35 kg/m2 * Able to understand the information sheet and willing to comply with study protocol * Able to give informed written consent
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Postprandial glycaemia (iAUC 0-30 min) | 30 min | The primary endpoint is iAUC 0-30 min for plasma glucose concentrations |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Postprandial glycaemia: Tmax | 120 min | Tmax for plasma glucose concentrations |
| Postprandial non-esterified fatty acids (NEFA): iAUC 0-120 min | 120 min | iAUC 0-120 min for serum NEFA concentrations |
| Postprandial blood peptide YY (PYY): iAUC 0-120 min | 120 min | iAUC 0-120 minfor plasma PYY concentrations |
| Postprandial blood peptide YY (PYY): iCmax | 120 min | iCmax for plasma PYY concentrations |
| Postprandial blood peptide YY (PYY): Tmax | 120 min | Tmax for plasma PYY concentrations |
| Postprandial blood peptide YY (PYY): Absolute concentrations at specific time points | 120 min | Absolute concentrations at specific time points, for plasma PYY concentrations |
| Postprandial glycaemia: iAUC 0-120 min | 120 min | iAUC 0-120 min for plasma glucose concentrations |
| Postprandial glycaemia: absolute concentrations at specific time points | 120 min | Absolute concentrations at specific time points, for plasma glucose concentrations |
| Postprandial insulinemia: iAUC 0-30 min | 30 min | iAUC 0-30 min for serum insulin concentrations |
| Postprandial insulinemia: iAUC 0-120 min | 120 min | iAUC 0-120 min for serum insulin concentrations |
| Postprandial insulinemia: iCmax | 120 min | iCmax, for serum insulin concentrations |
| Postprandial insulinemia: Tmax | 120 min | Tmax for serum insulin concentrations |
| Postprandial insulinemia: absolute concentrations at specific time points | 120 min | Absolute concentrations at specific time points, for serum insulin concentrations |
| Postprandial C-peptide: iAUC 0-30 min | 30 min | iAUC 0-30 min for plasma C-peptide concentrations |
| Postprandial C-peptide: iAUC 0-120 min | 30 min | iAUC 0-120 min for plasma C-peptide concentrations |
| Postprandial C-peptide: iCmax | 120 min | iCmax for plasma C-peptide concentrations |
| Postprandial C-peptide: Tmax | 120 min | Tmax for plasma C-peptide concentrations |
| Postprandial C-peptide: Absolute concentrations at specific time points | 120 min | Absolute concentrations at specific time points, for plasma C-peptide concentrations |
| Postprandial non-esterified fatty acids (NEFA): iAUC 0-30 min | 30 min | iAUC 0-30 min for serum NEFA concentrations |
| Postprandial glycaemia: iCmax | 120 min | iCmax for plasma glucose concentrations |
| Postprandial non-esterified fatty acids (NEFA): iCmax | 120 min | iCmax for serum NEFA concentrations |
| Postprandial non-esterified fatty acids (NEFA): Tmax | 120 min | Tmax for serum NEFA concentrations |
| Postprandial non-esterified fatty acids (NEFA): Absolute concentrations at specific time points | 120 min | Absolute concentrations at specific time points, for serum NEFA concentrations |
| Postprandial blood glucose-dependent insulinotropic peptide (GIP): iAUC 0-30 min | 30 min | iAUC 0-30 min for plasma GIP concentrations |
| Postprandial blood glucose-dependent insulinotropic peptide (GIP): iAUC 0-120 min | 120 min | iAUC 0-120 min for plasma GIP concentrations |
| Postprandial blood glucose-dependent insulinotropic peptide (GIP): iCmax | 120 min | iCmax, for plasma GIP concentrations |
| Postprandial blood glucose-dependent insulinotropic peptide (GIP): Tmax | 120 min | Tmax for plasma GIP concentrations |
| Postprandial blood glucose-dependent insulinotropic peptide (GIP): Absolute concentrations at specific time points | 120 min | Absolute concentrations at specific time points, for plasma GIP concentrations |
| Postprandial blood Glucagon-like peptide 1 (GLP-1): iAUC 0-30 min | 30 min | iAUC 0-30 min for plasma GLP-1 concentrations |
| Postprandial blood Glucagon-like peptide 1 (GLP-1): iAUC 0-120 min | 120 min | iAUC 0-120 min, for plasma GLP-1 concentrations |
| Postprandial blood Glucagon-like peptide 1 (GLP-1): iCmax | 120 min | iCmax for plasma GLP-1 concentrations |
| Postprandial blood Glucagon-like peptide 1 (GLP-1): Tmax | 30 min | Tmax for plasma GLP-1 concentrations |
| Postprandial blood Glucagon-like peptide 1 (GLP-1): Absolute concentrations at specific time points | 120 min | Absolute concentrations at specific time points, for plasma GLP-1 concentrations |
| Postprandial blood peptide YY (PYY): iAUC 0-30 min | 30 min | iAUC 0-30 min for plasma PYY concentrations |
Other
| Measure | Time frame | Description |
|---|---|---|
| VAS measures of the palatability of the study drink | 10 min following the test drink | Descriptive statistics |
| VAS measures of mood, satiety and digestive comfort | 120 min | Descriptive statistics |
| Buccal mouth swab | One off sample, collected at screening | Future exploratory analysis of lactase activity via the derived allele at the European lactase persistence (LP) locus |
| Food diary (estimated/unweighed) | 7-days, collected at screening | Habitual dietary intake analysis |
Countries
United Kingdom