» Articles » PMID: 35057557

Temporal Patterns of Glucagon and Its Relationships with Glucose and Insulin Following Ingestion of Different Classes of Macronutrients

Overview
Journal Nutrients
Date 2022 Jan 21
PMID 35057557
Authors
Affiliations
Soon will be listed here.
Abstract

Background: glucagon secretion and inhibition should be mainly determined by glucose and insulin levels, but the relative relevance of each factor is not clarified, especially following ingestion of different macronutrients. We aimed to investigate the associations between plasma glucagon, glucose, and insulin after ingestion of single macronutrients or mixed-meal.

Methods: thirty-six participants underwent four metabolic tests, based on administration of glucose, protein, fat, or mixed-meal. Glucagon, glucose, insulin, and C-peptide were measured at fasting and for 300 min following food ingestion. We analyzed relationships between time samples of glucagon, glucose, and insulin in each individual, as well as between suprabasal area-under-the-curve of the same variables (ΔAUC, ΔAUC, ΔAUC) over the whole participants' cohort.

Results: in individuals, time samples of glucagon and glucose were related in only 26 cases (18 direct, 8 inverse relationships), whereas relationship with insulin was more frequent (60 and 5, < 0.0001). The frequency of significant relationships was different among tests, especially for direct relationships ( ≤ 0.006). In the whole cohort, ΔAUC was weakly related to ΔAUC ( ≤ 0.02), but not to ΔAUC, though basal insulin secretion emerged as possible covariate.

Conclusions: glucose and insulin are not general and exclusive determinants of glucagon secretion/inhibition after mixed-meal or macronutrients ingestion.

Citing Articles

Glucagon kinetics assessed by mathematical modelling during oral glucose administration in people spanning from normal glucose tolerance to type 2 diabetes.

Andreozzi F, Mancuso E, Rubino M, Salvatori B, Morettini M, Monea G Front Endocrinol (Lausanne). 2024; 15:1376530.

PMID: 38681771 PMC: 11045965. DOI: 10.3389/fendo.2024.1376530.


Robust increase in glucagon secretion after oral protein intake, but not after glucose or lipid intake in Japanese people without diabetes.

Ichikawa R, Takano K, Fujimoto K, Kobayashi M, Kitamura T, Shichiri M J Diabetes Investig. 2023; 14(10):1172-1174.

PMID: 37480216 PMC: 10512907. DOI: 10.1111/jdi.14053.


Chemical Compounds and Ambient Factors Affecting Pancreatic Alpha-Cells Mass and Function: What Evidence?.

Mannino G, Mancuso E, Sbrignadello S, Morettini M, Andreozzi F, Tura A Int J Environ Res Public Health. 2022; 19(24).

PMID: 36554367 PMC: 9778390. DOI: 10.3390/ijerph192416489.


The relationship between insulin and glucagon concentrations in non-diabetic humans.

Laurenti M, Arora P, Dalla Man C, Andrews J, Rizza R, Matveyenko A Physiol Rep. 2022; 10(13):e15380.

PMID: 35822422 PMC: 9277417. DOI: 10.14814/phy2.15380.

References
1.
Ahren B . Glucagon--Early breakthroughs and recent discoveries. Peptides. 2015; 67:74-81. DOI: 10.1016/j.peptides.2015.03.011. View

2.
Pipeleers D, Schuit F, Int Veld P, Maes E, Hooghe-Peters E, Van De Winkel M . Interplay of nutrients and hormones in the regulation of insulin release. Endocrinology. 1985; 117(3):824-33. DOI: 10.1210/endo-117-3-824. View

3.
Zhang Q, Ramracheya R, Lahmann C, Tarasov A, Bengtsson M, Braha O . Role of KATP channels in glucose-regulated glucagon secretion and impaired counterregulation in type 2 diabetes. Cell Metab. 2013; 18(6):871-82. PMC: 3851686. DOI: 10.1016/j.cmet.2013.10.014. View

4.
Gromada J, Chabosseau P, Rutter G . The α-cell in diabetes mellitus. Nat Rev Endocrinol. 2018; 14(12):694-704. DOI: 10.1038/s41574-018-0097-y. View

5.
Bolli G, Dimitriadis G, Pehling G, Baker B, Haymond M, Cryer P . Abnormal glucose counterregulation after subcutaneous insulin in insulin-dependent diabetes mellitus. N Engl J Med. 1984; 310(26):1706-11. DOI: 10.1056/NEJM198406283102605. View