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      The effect of exogenous glucagon on circulating amino acids in individuals with and without type 2 diabetes and obesity

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          Abstract

          Objective

          In obesity and type 2 diabetes, hyperglucagonaemia may be caused by elevated levels of glucagonotropic amino acids due to hepatic glucagon resistance at the level of amino acid turnover. Here, we investigated the effect of exogenous glucagon on circulating amino acids in obese and non-obese individuals with and without type 2 diabetes.

          Design

          This was a post hoc analysis in a glucagon infusion study performed in individuals with type 2 diabetes ( n = 16) and in age, sex, and body mass index-matched control individuals without diabetes ( n = 16). Each group comprised two subgroups of eight individuals with and without obesity, respectively.

          Methods

          All participants received a 1-h glucagon infusion (4 ng/kg/min) in the overnight fasted state. Plasma amino acid concentrations were measured with frequent intervals.

          Results

          Compared to the control subgroup without obesity, baseline total amino acid levels were elevated in the control subgroup with obesity and in the type 2 diabetes subgroup without obesity. In all subgroups, amino acid levels decreased by up to 20% in response to glucagon infusion, which resulted in high physiological steady-state glucagon levels (mean concentration: 74 pmol/L, 95% CI [68;79] pmol/L). Following correction for multiple testing, no intergroup differences in changes in amino acid levels reached significance.

          Conclusion

          Obesity and type 2 diabetes status was associated with elevated fasting levels of total amino acids. The glucagon infusion decreased circulating amino acid levels similarly in all subgroups, without significant differences in the response to exogenous glucagon between individuals with and without obesity and type 2 diabetes.

          Significance statement

          The hormone glucagon stimulates glucose production from the liver, which may promote hyperglycaemia if glucagon levels are abnormally elevated, as is often seen in type 2 diabetes and obesity. Glucagon levels are closely linked to, and influenced by, the levels of circulating amino acids. To further investigate this link, we measured amino acid levels in individuals with and without obesity and type 2 diabetes before and during an infusion of glucagon. We found that circulating amino acid levels were higher in type 2 diabetes and obesity, and that glucagon infusion decreased amino acid levels in both individuals with and without type 2 diabetes and obesity. The study adds novel information to the link between circulating levels of glucagon and amino acids.

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          Most cited references22

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Physiology of proglucagon peptides: role of glucagon and GLP-1 in health and disease.

            The preproglucagon gene (Gcg) is expressed by specific enteroendocrine cells (L-cells) of the intestinal mucosa, pancreatic islet α-cells, and a discrete set of neurons within the nucleus of the solitary tract. Gcg encodes multiple peptides including glucagon, glucagon-like peptide-1, glucagon-like peptide-2, oxyntomodulin, and glicentin. Of these, glucagon and GLP-1 have received the most attention because of important roles in glucose metabolism, involvement in diabetes and other disorders, and application to therapeutics. The generally accepted model is that GLP-1 improves glucose homeostasis indirectly via stimulation of nutrient-induced insulin release and by reducing glucagon secretion. Yet the body of literature surrounding GLP-1 physiology reveals an incompletely understood and complex system that includes peripheral and central GLP-1 actions to regulate energy and glucose homeostasis. On the other hand, glucagon is established principally as a counterregulatory hormone, increasing in response to physiological challenges that threaten adequate blood glucose levels and driving glucose production to restore euglycemia. However, there also exists a potential role for glucagon in regulating energy expenditure that has recently been suggested in pharmacological studies. It is also becoming apparent that there is cross-talk between the proglucagon derived-peptides, e.g., GLP-1 inhibits glucagon secretion, and some additive or synergistic pharmacological interaction between GLP-1 and glucagon, e.g., dual glucagon/GLP-1 agonists cause more weight loss than single agonists. In this review, we discuss the physiological functions of both glucagon and GLP-1 by comparing and contrasting how these peptides function, variably in concert and opposition, to regulate glucose and energy homeostasis.
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              Transient elastography (FibroScan(®)) with controlled attenuation parameter in the assessment of liver steatosis and fibrosis in patients with nonalcoholic fatty liver disease - Where do we stand?

              Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease worldwide. Currently, the routinely used modalities are unable to adequately determine the levels of steatosis and fibrosis (laboratory tests and ultrasonography) or cannot be applied as a screening procedure (liver biopsy). Among the non-invasive tests, transient elastography (FibroScan(®), TE) with controlled attenuation parameter (CAP) has demonstrated good accuracy in quantifying the levels of liver steatosis and fibrosis in patients with NAFLD, the factors associated with the diagnosis and NAFLD progression. The method is fast, reliable and reproducible, with good intra- and interobserver levels of agreement, thus allowing for population-wide screening and disease follow-up. The initial inability of the procedure to accurately determine fibrosis and steatosis in obese patients has been addressed with the development of the obese-specific XL probe. TE with CAP is a viable alternative to ultrasonography, both as an initial assessment and during follow-up of patients with NAFLD. Its ability to exclude patients with advanced fibrosis may be used to identify low-risk NAFLD patients in whom liver biopsy is not needed, therefore reducing the risk of complications and the financial costs.

                Author and article information

                Journal
                Endocr Connect
                Endocr Connect
                EC
                Endocrine Connections
                Bioscientifica Ltd (Bristol )
                2049-3614
                21 February 2024
                26 January 2024
                01 March 2024
                : 13
                : 3
                : e230516
                Affiliations
                [1 ]Center for Clinical Metabolic Research , Gentofte Hospital, University of Copenhagen, Hellerup, Denmark
                [2 ]Clinical Research , Steno Diabetes Center Copenhagen, Herlev, Denmark
                [3 ]Department of Clinical Biochemistry , Clinical Metabolomics Core Facility, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
                [4 ]Department of Biomedical Sciences , Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
                [5 ]Department of Clinical Biochemistry , University Hospital Copenhagen, Bispebjerg, Copenhagen, Denmark
                [6 ]Novo Nordisk Foundation Center for Basic Metabolic Research , Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
                [7 ]Department of Clinical Medicine , Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
                [8 ]Department of Clinical Pharmacology , Copenhagen University Hospital – Bispebjerg and Frederiksberg, Copenhagen, Denmark
                [9 ]Copenhagen Center for Translational Research , Copenhagen University Hospital – Bispebjerg and Frederiksberg, University of Copenhagen, Copenhagen, Denmark
                Author notes
                Correspondence should be addressed to F K Knop: filip.krag.knop.01@ 123456regionh.dk
                Author information
                http://orcid.org/0000-0002-2495-5034
                Article
                EC-23-0516
                10.1530/EC-23-0516
                10959036
                38276866
                c662bd90-5ea9-4848-a04d-87b1fb88dc85
                © the author(s)

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 08 December 2023
                : 26 January 2024
                Funding
                Funded by: Novo Nordisk, doi http://dx.doi.org/10.13039/501100004191;
                Categories
                Research

                amino acids,glucagon,obesity,type 2 diabetes
                amino acids, glucagon, obesity, type 2 diabetes

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