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The Effect of Buffering High Acid Load Meal with Sodium Bicarbonate on Postprandial Glucose Metabolism in Humans-A Randomized Placebo-Controlled Study

Abstract

Background: High dietary acid load relates to increased risk of type 2 diabetes in epidemiological studies. We aimed to investigate whether buffering a high acid load meal with an alkalizing treatment changes glucose metabolism post meal. Methods: Non-diabetic participants (n = 32) were randomized to receive either 1680 mg NaHCO(3) or placebo, followed by a high acid load meal in a double-blind placebo-controlled crossover (1-4 weeks apart) study. Thirty (20 men) participants completed the study. Venous blood pH, serum bicarbonate, blood glucose, serum insulin, C-peptide, non-esterified fatty acid (NEFA), and plasma glucagon-like peptide-1 (GLP-1) concentrations were measured at baseline (fasting) and at 15-30 min intervals for 3 h post meal. Results: The treatment was well tolerated. Venous blood pH declined in the first 15 min post meal with the placebo (p = 0.001), but not with NaHCO(3) (p = 0.86) and remained decreased with the placebo for 3 h (pinteraction = 0.04). On average over the 3 h blood pH iAUC was greater with NaHCO(3) compared with placebo (p = 0.02). However, postprandial glucose, insulin, C-peptide, NEFA and GLP-1 were not different between treatments (pinteraction >/= 0.07). Conclusions: An alkalizing medication administered pre-meal has no acute effect on glycaemia and insulin response in healthy individuals. Long-term interventions in at-risk populations are necessary to investigate the effect of sustained alkalization on glucose metabolism.

Type Journal
ISBN 2072-6643 (Electronic) 2072-6643 (Linking)
Authors Kozan, P.; Blythe, J. C.; Greenfield, J. R.; Samocha-Bonet, D.
Responsible Garvan Author Associate Professor Dorit Samocha-Bonet
Publisher Name Nutrients
Published Date 2017-08-11
Published Volume 9
Published Issue 8
Published Pages e861
Status Always Electronic
DOI 10.3390/nu9080861
URL link to publisher's version https://www.ncbi.nlm.nih.gov/pubmed/28800090
OpenAccess link to author's accepted manuscript version https://publications.gimr.garvan.org.au/open-access/14107