Drinks containing anthocyanin-rich blackcurrant extract decrease postprandial blood glucose, insulin and incretin concentrations

Monica L Castro-Acosta, Leanne Smith, Rosalind J Miller, Danielle I McCarthy, Jonathan A Farrimond, Wendy L Hall, Monica L Castro-Acosta, Leanne Smith, Rosalind J Miller, Danielle I McCarthy, Jonathan A Farrimond, Wendy L Hall

Abstract

Blackcurrants are rich in polyphenolic glycosides called anthocyanins, which may inhibit postprandial glycemia. The aim was to determine the dose-dependent effects of blackcurrant extract on postprandial glycemia. Men and postmenopausal women (14M, 9W, mean age 46 years, S.D.=14) were enrolled into a randomized, double-blind, crossover trial. Low sugar fruit drinks containing blackcurrant extract providing 150-mg (L-BE), 300-mg (M-BE) and 600-mg (H-BE) total anthocyanins or no blackcurrant extract (CON) were administered immediately before a high-carbohydrate meal. Plasma glucose, insulin and incretins (GIP and GLP-1) were measured 0-120min, and plasma 8-isoprostane F2α, together with arterial stiffness by digital volume pulse (DVP) was measured at 0 and 120min. Early plasma glucose response was significantly reduced following H-BE (n=22), relative to CON, with a mean difference (95% CI) in area over baseline (AOB) 0-30min of -0.34mmol/l.h (-0.56, -0.11, P<.005); there were no differences between the intermediate doses and placebo. Plasma insulin concentrations (AOB 0-30min) were similarly reduced. Plasma GIP concentrations (AOB 0-120min) were significantly reduced following H-BE, with a mean difference of -46.6ng/l.h (-66.7, -26.5, P<.0001) compared to CON. Plasma GLP-1 concentrations were reduced following H-BE at 90min. There were no effects on 8-isoprostane F2α or vascular function. Consumption of blackcurrant extract in amounts roughly equivalent to 100-g blackcurrants reduced postprandial glycemia, insulinemia and incretin secretion, which suggests that inclusion of blackcurrant polyphenols in foods may provide cardio-metabolic health benefits. This trial was registered at clinicaltrials.gov as NCT01706653.

Keywords: Anthocyanins; Berries; Incretins; Insulin; Polyphenols; Postprandial glycemia; Randomized controlled trial.

Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.

Figures

Fig. 1
Fig. 1
Study visit protocol.
Fig. 2
Fig. 2
Consort diagram.
Fig. 3
Fig. 3
Postprandial plasma glucose and insulin concentrations. Mean (±S.E.M.) plasma glucose (A) and insulin (B) concentrations following ingestion of four low sugar fruit drinks 2 min before consuming a mixed carbohydrate meal, in randomized order: H-BE: high blackcurrant extract; M-BE: medium blackcurrant extract; L-BE: low blackcurrant extract; CON: placebo. N=22. All data were natural log transformed before mixed model analysis. For glucose P<.001 for an overall drink effect on changes from baseline, and for insulin, P<.001 for a drink effect and P<.001 for a drink x time interaction on raw values and changes from baseline. (A) post hoc analysis of timepoint differences in change from baseline in glucose compared to CON with Dunnett's adjustment: aP<0.05 for the difference between H-BE and CON and M-BE and CON; bP<.005 for the difference between H-BE and CON; cP<0.01 for the difference between H-BE and CON. (B) post hoc analysis of timepoint differences in change from baseline in insulin with Dunnett's adjustment: aP<.005 for the difference between H-BE and CON; bP<0.01 for the difference between H-BE and CON; cP<0.05 for the difference between H-BE and CON.
Fig. 4
Fig. 4
Postprandial plasma GIP and GLP-1 concentrations. Mean (±S.E.M.) plasma GIP (A) and GLP-1 (B) concentrations following ingestion of four low sugar fruit drinks 2 min before consuming a mixed carbohydrate meal, in randomized order: H-BE: high blackcurrant extract (GIP n=17; GLP-1 n=20); M-BE: medium blackcurrant extract (GIP n=20; GLP-1 n=22); L-BE: low blackcurrant extract (GIP n=20; GLP-1 n=21); CON: placebo (GIP n=19; GLP-1 n=22). All data were natural log transformed before mixed model analysis. For GIP, there was an overall drink effect on raw values (P<.0001) and changes from baseline (P<.0001) and a drink × time interaction on raw values (P<0.005), and for GLP-1, there was an overall drink effect on raw values and changes from baseline (P<.001). (A) post hoc analysis of timepoint differences in change from baseline in GIP with Dunnett's adjustment: aP<0.0001 for the difference between H-BE and CON and bP<0.001 for the difference between L-BE and CON; cP<0.0005 for the difference between H-BE and CON; dP<0.005 for the difference between H-BE and L-BE and H-BE and M-BE; eP<0.05 for the difference between H-BE and CON; and fP<0.0005 for the difference between H-BE and CON. (B) post hoc analysis of timepoint differences in change from baseline in GLP-1 with Dunnett's adjustment: aP<0.05 for the difference between H-BE and CON.

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Source: PubMed

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