Literature DB >> 25176602

Relationship between whole-body macronutrient oxidative partitioning and pancreatic insulin secretion/β-cell function in non-diabetic humans.

Jose E Galgani1, Maria L Mizgier2, Andrea Mari3, Eric Ravussin4.   

Abstract

BACKGROUND: Glucose-stimulated insulin secretion correlates inversely with the degree of whole-body insulin sensitivity suggesting a crosstalk between peripheral organs and pancreas. Such sensing mechanism could be mediated by changes in glucose flux (uptake, oxidation or storage) in peripheral tissues that may drive insulin secretion. AIM: To relate whole-body non-protein respiratory quotient (npRQ), an index of macronutrient oxidative partitioning, with insulin secretion and β-cell function in non-diabetic individuals.
METHODS: Macronutrient oxidation was measured after an overnight fast and for 4h after a 75-g oral glucose tolerance test (OGTT) in 30 participants (15/15 males/females; 35±12y; 27±4kg/m(2)). Furthermore, npRQ was assessed for 24h in a metabolic chamber. Insulin secretion was estimated by deconvolution of serum C-peptide concentration (fasting and 4-h OGTT) and from 24-h urinary C-peptide excretion corrected for energy intake (metabolic chamber). β-Cell function parameters were obtained by mathematical modeling, while insulin sensitivity was determined by a euglycemic-hyperinsulinemic clamp (120mU·m(-2)·min(-1)).
RESULTS: Insulin secretion (from 24-h urinary C-peptide) correlated inversely with 24-h npRQ (r=-0.61; p=0.001), even after controlling for insulin sensitivity, energy balance, age and body mass index (r=-0.52; p=0.01). In turn, insulin secretion (from serum C-peptide) was not associated with fasting or OGTT npRQ. However, fasting npRQ was positively correlated with rate sensitivity (r=0.40; p<0.05) and marginally with glucose sensitivity (r=0.34; p=0.08).
CONCLUSION: Macronutrient oxidative partitioning, specifically glucose oxidation, might play a role on the regulation of insulin secretion. Further studies should aim at identifying the signals linking these processes.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Glucose flux; Insulin resistance; Respiratory quotient; Skeletal muscle

Mesh:

Substances:

Year:  2014        PMID: 25176602      PMCID: PMC4198668          DOI: 10.1016/j.metabol.2014.08.002

Source DB:  PubMed          Journal:  Metabolism        ISSN: 0026-0495            Impact factor:   8.694


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