FGF21 is an insulin-dependent postprandial hormone in adult humans

التفاصيل البيبلوغرافية
العنوان: FGF21 is an insulin-dependent postprandial hormone in adult humans
المؤلفون: James W. Perfield, Christopher J. Gaffney, Francis B. Stephens, Dennis P. Smith, Jo E. Lewis, Francis J. P. Ebling, Christine C. Cheng, Luke Norton, Ricardo J. Samms, Andrew C. Adams, Kostas Tsintzas, Tony Butterfield
بيانات النشر: Oxford University Press
مصطلحات موضوعية: 0301 basic medicine, Adult, Blood Glucose, Male, medicine.medical_specialty, FGF21, Endocrinology, Diabetes and Metabolism, medicine.medical_treatment, Clinical Biochemistry, 030209 endocrinology & metabolism, Type 2 diabetes, Biology, Diet, High-Fat, Biochemistry, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Endocrinology, Internal medicine, Diabetes mellitus, medicine, Hyperinsulinemia, Humans, Insulin, Clinical Research Articles, Glucose tolerance test, medicine.diagnostic_test, Biochemistry (medical), Glucose clamp technique, Glucose Tolerance Test, Middle Aged, medicine.disease, Postprandial Period, Fibroblast Growth Factors, 030104 developmental biology, Postprandial, Glucose, Diabetes Mellitus, Type 2, Glucose Clamp Technique, Female, Signal Transduction
الوصف: Context Fibroblast growth factor 21 (FGF21) secretion has been shown to respond directly to carbohydrate consumption, with glucose, fructose, and sucrose all reported to increase plasma levels of FGF21 in rodents and humans. However, carbohydrate consumption also results in secretion of insulin. Objective The aim of this study was to examine the combined and independent effects of hyperglycemia and hyperinsulinemia on total and bioactive FGF21 in the postprandial period in humans, and determine whether this effect is attenuated in conditions of altered insulin secretion and action. Methods Circulating glucose, insulin, total and bioactive FGF21, and fibroblast activation protein were measured in adults with and without type 2 diabetes (T2D) following an oral glucose tolerance test (OGTT), and under a series of insulin and glucose clamp conditions and following high-fat diet in healthy adults. Results Circulating total and bioactive FGF21 levels responded acutely to OGTT, and their ratio was attenuated in T2D patients with reduced postprandial insulin response. The clamp studies revealed that insulin but not glucose accounts for the postprandial rise in FGF21. Finally, there was an attenuated rise in FGF21 in response to a high-fat dietary intervention that is known to alter insulin-stimulated substrate utilization in metabolically active tissues. Conclusions Insulin rather than glucose per se increases total and bioactive FGF21 in the postprandial period in adult humans. Understanding the impact of T2D on bioactive FGF21 will have a significant effect upon the efficacy of therapeutic agents designed to target the FGF21 pathway.
وصف الملف: PDF
اللغة: English
تدمد: 0021-972X
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3065d11da150d0f10f621ba4bcbf0d14Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....3065d11da150d0f10f621ba4bcbf0d14
قاعدة البيانات: OpenAIRE