Integrated glucagon model for estimation of α-cell responsivity to glucose and amino acids during graded glucose infusion.

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Federica Boscolo, Sneha Mohan, Marcello C Laurenti, Jacob Kohlenberg, Hannah E Christie, Aoife M Egan, Adrian Vella, Chiara Dalla Man
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引用次数: 0

Abstract

Pancreatic α-cells secrete glucagon. The glucagon secretion rate (GSR) increases when plasma glucose decreases; conversely, GSR decreases when glucose rises. In addition, amino acids (AAs) stimulate GSR. Impaired GSR suppression by glucose contributes to postprandial hyperglycemia in individuals with impaired glucose tolerance, obesity, and type 2 diabetes (T2D). However, the current method to assess α-cell responsivity to glucose ignores the contribution of AAs and is a two-step approach with some limitations. To address this, we developed a model-based method to quantify α-cell responsivity to glucose during a graded glucose infusion, in the presence and absence of AAs. A total of 52 subjects were studied. Thirty-seven subjects from study 1 [13 M, age = 54 ± 10 yr, body mass index (BMI) = 30 ± 5 kg/m2] were studied once. Fifteen subjects (4 M, age = 47 ± 11 yr, BMI = 28 ± 4 kg/m2) from study 2 were studied twice: once with saline and once with an AA infusion (Clinisol 15%, 0.003 mL/kg/min). Plasma glucagon, glucose, and AA concentrations were measured over 240 min. We tested several mathematical models of GSR, and the best one was selected using standard criteria. The optimal model describes GSR as an exponential decay driven by delayed plasma glucose concentration and modulated by AAs. The model provides an index of α-cell responsivity, G50, i.e., the glucose increase required to suppress GSR by 50%. AA infusion increased G50 compared with the saline infusion. This model-based approach provides an index of α-cell responsiveness under both physiological and AA-stimulated conditions. Its use may help in the early detection of α-cell dysfunction in people at risk of developing T2D.NEW & NOTEWORTHY In this study, we propose two new mathematical models able to quantify glucagon secretion during a graded glucose infusion, in the presence and absence of amino acids. The models provide an index of α-cell responsivity, G50, i.e., the glucose increase required to suppress glucose secretion rate (GSR) by 50%. Results show that the presence of amino acids reduced α-cell responsivity to glucose.

综合胰高血糖素模型评估分级葡萄糖输注过程中α细胞对葡萄糖和氨基酸的反应。
胰腺α-细胞分泌胰高血糖素。胰高血糖素分泌率(GSR)随血糖降低而升高;相反,当葡萄糖升高时,GSR降低。此外,氨基酸(AA)刺激GSR。葡萄糖对GSR的抑制受损会导致糖耐量受损、肥胖和2型糖尿病(T2D)患者餐后高血糖。然而,目前评估α-细胞对葡萄糖的反应性的方法忽略了AA的贡献,并且是两步法,具有一定的局限性。为了解决这个问题,我们开发了一种基于模型的方法来量化分级葡萄糖输注期间α-细胞对葡萄糖的反应,无论是否存在AA。共研究了52名受试者。研究1的37例受试者(13M,年龄=54±10岁,BMI=30±5 kg/m²)进行了一次研究。研究2的15名受试者(年龄47±11岁,BMI=28±4 kg/m²)进行了两次研究:一次注射生理盐水,一次注射AA (Clinisol 15%, 0.003 mL/kg/min)。240分钟后测定血浆胰高血糖素、葡萄糖和AA浓度。我们测试了几种GSR的数学模型,并使用标准准则选择了最佳模型。最优模型将GSR描述为由延迟血浆葡萄糖浓度驱动并由AA调节的指数衰减。该模型提供α-细胞反应性指数G50,即抑制GSR 50%所需的葡萄糖增加量。与生理盐水输注相比,AA输注使G50升高。这种基于模型的方法提供了生理和aa刺激条件下α-细胞反应性的指标。它的使用可能有助于早期发现有患T2D风险的人α-细胞功能障碍。
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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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