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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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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 |
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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 |
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