Cargando…

Gastric bypass alters both glucose-dependent and glucose-independent regulation of islet hormone secretion

AIMS: Roux-en-Y gastric bypass surgery (GB) is characterized by accentuated, but short-lived postprandial elevations of blood glucose and insulin. This profile has been attributed to effects of relative hyperglycemia to directly stimulate β-cells and an augmented incretin effect. We hypothesized add...

Descripción completa

Detalles Bibliográficos
Autores principales: Salehi, Marzieh, Woods, Stephen C., D’Alessio, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586360/
https://www.ncbi.nlm.nih.gov/pubmed/26316298
http://dx.doi.org/10.1002/oby.21186
_version_ 1782392346953908224
author Salehi, Marzieh
Woods, Stephen C.
D’Alessio, David A.
author_facet Salehi, Marzieh
Woods, Stephen C.
D’Alessio, David A.
author_sort Salehi, Marzieh
collection PubMed
description AIMS: Roux-en-Y gastric bypass surgery (GB) is characterized by accentuated, but short-lived postprandial elevations of blood glucose and insulin. This profile has been attributed to effects of relative hyperglycemia to directly stimulate β-cells and an augmented incretin effect. We hypothesized additional glucose-independent stimulation of insulin secretion in GB subjects. METHODS: Fifteen subjects with prior GB, and six matched obese non-surgical controls, and seven lean individuals were recruited. Islet hormones were measured before and after meal ingestion during hyperinsulinemic hypoglycemic clamps to minimize the direct effects of glycemia and glucose-dependent gastrointestinal hormones on insulin secretion. RESULTS: The GB subjects had less suppression of fasting β-cell secretion during the insulin clamp compared to controls. In addition, meal-induced insulin secretion increased in the GB subjects but not controls during fixed sub-basal glycemia. In contrast the glucagon responses to hypoglycemia and meal ingestion were lower in the GB subjects than controls. CONCLUSIONS: Among subjects with GB the response of insulin and glucagon secretion to decreasing blood glucose is blunted, but meal-induced insulin secretion is stimulated even at fixed systemic sub-basal glycemia. These findings indicate that following GB islet hormone secretion is altered as a result of factors beyond circulatory glucose levels.
format Online
Article
Text
id pubmed-4586360
institution National Center for Biotechnology Information
language English
publishDate 2015
record_format MEDLINE/PubMed
spelling pubmed-45863602016-05-18 Gastric bypass alters both glucose-dependent and glucose-independent regulation of islet hormone secretion Salehi, Marzieh Woods, Stephen C. D’Alessio, David A. Obesity (Silver Spring) Article AIMS: Roux-en-Y gastric bypass surgery (GB) is characterized by accentuated, but short-lived postprandial elevations of blood glucose and insulin. This profile has been attributed to effects of relative hyperglycemia to directly stimulate β-cells and an augmented incretin effect. We hypothesized additional glucose-independent stimulation of insulin secretion in GB subjects. METHODS: Fifteen subjects with prior GB, and six matched obese non-surgical controls, and seven lean individuals were recruited. Islet hormones were measured before and after meal ingestion during hyperinsulinemic hypoglycemic clamps to minimize the direct effects of glycemia and glucose-dependent gastrointestinal hormones on insulin secretion. RESULTS: The GB subjects had less suppression of fasting β-cell secretion during the insulin clamp compared to controls. In addition, meal-induced insulin secretion increased in the GB subjects but not controls during fixed sub-basal glycemia. In contrast the glucagon responses to hypoglycemia and meal ingestion were lower in the GB subjects than controls. CONCLUSIONS: Among subjects with GB the response of insulin and glucagon secretion to decreasing blood glucose is blunted, but meal-induced insulin secretion is stimulated even at fixed systemic sub-basal glycemia. These findings indicate that following GB islet hormone secretion is altered as a result of factors beyond circulatory glucose levels. 2015-08-28 2015-10 /pmc/articles/PMC4586360/ /pubmed/26316298 http://dx.doi.org/10.1002/oby.21186 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Salehi, Marzieh
Woods, Stephen C.
D’Alessio, David A.
Gastric bypass alters both glucose-dependent and glucose-independent regulation of islet hormone secretion
title Gastric bypass alters both glucose-dependent and glucose-independent regulation of islet hormone secretion
title_full Gastric bypass alters both glucose-dependent and glucose-independent regulation of islet hormone secretion
title_fullStr Gastric bypass alters both glucose-dependent and glucose-independent regulation of islet hormone secretion
title_full_unstemmed Gastric bypass alters both glucose-dependent and glucose-independent regulation of islet hormone secretion
title_short Gastric bypass alters both glucose-dependent and glucose-independent regulation of islet hormone secretion
title_sort gastric bypass alters both glucose-dependent and glucose-independent regulation of islet hormone secretion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586360/
https://www.ncbi.nlm.nih.gov/pubmed/26316298
http://dx.doi.org/10.1002/oby.21186
work_keys_str_mv AT salehimarzieh gastricbypassaltersbothglucosedependentandglucoseindependentregulationofislethormonesecretion
AT woodsstephenc gastricbypassaltersbothglucosedependentandglucoseindependentregulationofislethormonesecretion
AT dalessiodavida gastricbypassaltersbothglucosedependentandglucoseindependentregulationofislethormonesecretion