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Loss of Inverse Relationship Between Pulsatile Insulin and Glucagon Secretion in Patients With Type 2 Diabetes

OBJECTIVE: In patients with type 2 diabetes, glucagon levels are often increased. Furthermore, pulsatile secretion of insulin is disturbed in such patients. Whether pulsatile glucagon secretion is altered in type 2 diabetes is not known. RESEARCH DESIGN AND METHODS: Twelve patients with type 2 diabe...

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Autores principales: Menge, Björn A., Grüber, Lena, Jørgensen, Signe M., Deacon, Carolyn F., Schmidt, Wolfgang E., Veldhuis, Johannes D., Holst, Jens J., Meier, Juris J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142077/
https://www.ncbi.nlm.nih.gov/pubmed/21677283
http://dx.doi.org/10.2337/db11-0251
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author Menge, Björn A.
Grüber, Lena
Jørgensen, Signe M.
Deacon, Carolyn F.
Schmidt, Wolfgang E.
Veldhuis, Johannes D.
Holst, Jens J.
Meier, Juris J.
author_facet Menge, Björn A.
Grüber, Lena
Jørgensen, Signe M.
Deacon, Carolyn F.
Schmidt, Wolfgang E.
Veldhuis, Johannes D.
Holst, Jens J.
Meier, Juris J.
author_sort Menge, Björn A.
collection PubMed
description OBJECTIVE: In patients with type 2 diabetes, glucagon levels are often increased. Furthermore, pulsatile secretion of insulin is disturbed in such patients. Whether pulsatile glucagon secretion is altered in type 2 diabetes is not known. RESEARCH DESIGN AND METHODS: Twelve patients with type 2 diabetes and 13 nondiabetic individuals were examined in the fasting state and after mixed meal ingestion. Deconvolution analyses were performed on insulin and glucagon concentration time series sampled at 1-min intervals. RESULTS: Both insulin and glucagon were secreted in distinct pulses, occurring at ∼5-min intervals. In patients with diabetes, postprandial insulin pulse mass was reduced by 74% (P < 0.001). Glucagon concentrations were increased in the patients during fasting and after meal ingestion (P < 0.05), specifically through an increased glucagon pulse mass (P < 0.01). In healthy subjects, the increase in postprandial insulin levels was inversely related to respective glucagon levels (P < 0.05). This relationship was absent in the fasting state and in patients with diabetes. CONCLUSIONS: Glucagon and insulin are secreted in a coordinated, pulsatile manner. A plausible model is that the postprandial increase in insulin burst mass represses the corresponding glucagon pulses. Disruption of the insulin–glucagon interaction in patients with type 2 diabetes could potentially contribute to hyperglucagonemia.
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spelling pubmed-31420772012-08-01 Loss of Inverse Relationship Between Pulsatile Insulin and Glucagon Secretion in Patients With Type 2 Diabetes Menge, Björn A. Grüber, Lena Jørgensen, Signe M. Deacon, Carolyn F. Schmidt, Wolfgang E. Veldhuis, Johannes D. Holst, Jens J. Meier, Juris J. Diabetes Pathophysiology OBJECTIVE: In patients with type 2 diabetes, glucagon levels are often increased. Furthermore, pulsatile secretion of insulin is disturbed in such patients. Whether pulsatile glucagon secretion is altered in type 2 diabetes is not known. RESEARCH DESIGN AND METHODS: Twelve patients with type 2 diabetes and 13 nondiabetic individuals were examined in the fasting state and after mixed meal ingestion. Deconvolution analyses were performed on insulin and glucagon concentration time series sampled at 1-min intervals. RESULTS: Both insulin and glucagon were secreted in distinct pulses, occurring at ∼5-min intervals. In patients with diabetes, postprandial insulin pulse mass was reduced by 74% (P < 0.001). Glucagon concentrations were increased in the patients during fasting and after meal ingestion (P < 0.05), specifically through an increased glucagon pulse mass (P < 0.01). In healthy subjects, the increase in postprandial insulin levels was inversely related to respective glucagon levels (P < 0.05). This relationship was absent in the fasting state and in patients with diabetes. CONCLUSIONS: Glucagon and insulin are secreted in a coordinated, pulsatile manner. A plausible model is that the postprandial increase in insulin burst mass represses the corresponding glucagon pulses. Disruption of the insulin–glucagon interaction in patients with type 2 diabetes could potentially contribute to hyperglucagonemia. American Diabetes Association 2011-08 2011-07-18 /pmc/articles/PMC3142077/ /pubmed/21677283 http://dx.doi.org/10.2337/db11-0251 Text en © 2011 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Pathophysiology
Menge, Björn A.
Grüber, Lena
Jørgensen, Signe M.
Deacon, Carolyn F.
Schmidt, Wolfgang E.
Veldhuis, Johannes D.
Holst, Jens J.
Meier, Juris J.
Loss of Inverse Relationship Between Pulsatile Insulin and Glucagon Secretion in Patients With Type 2 Diabetes
title Loss of Inverse Relationship Between Pulsatile Insulin and Glucagon Secretion in Patients With Type 2 Diabetes
title_full Loss of Inverse Relationship Between Pulsatile Insulin and Glucagon Secretion in Patients With Type 2 Diabetes
title_fullStr Loss of Inverse Relationship Between Pulsatile Insulin and Glucagon Secretion in Patients With Type 2 Diabetes
title_full_unstemmed Loss of Inverse Relationship Between Pulsatile Insulin and Glucagon Secretion in Patients With Type 2 Diabetes
title_short Loss of Inverse Relationship Between Pulsatile Insulin and Glucagon Secretion in Patients With Type 2 Diabetes
title_sort loss of inverse relationship between pulsatile insulin and glucagon secretion in patients with type 2 diabetes
topic Pathophysiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142077/
https://www.ncbi.nlm.nih.gov/pubmed/21677283
http://dx.doi.org/10.2337/db11-0251
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