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Preproglucagon Products and Their Respective Roles Regulating Insulin Secretion.
- Source :
-
Endocrinology [Endocrinology] 2021 Oct 01; Vol. 162 (10). - Publication Year :
- 2021
-
Abstract
- Historically, intracellular function and metabolic adaptation within the α-cell has been understudied, with most of the attention being placed on the insulin-producing β-cells due to their role in the pathophysiology of type 2 diabetes mellitus. However, there is a growing interest in understanding the function of other endocrine cell types within the islet and their paracrine role in regulating insulin secretion. For example, there is greater appreciation for α-cell products and their contributions to overall glucose homeostasis. Several recent studies have addressed a paracrine role for α-cell-derived glucagon-like peptide-1 (GLP-1) in regulating glucose homeostasis and responses to metabolic stress. Further, other studies have demonstrated the ability of glucagon to impact insulin secretion by acting through the GLP-1 receptor. These studies challenge the central dogma surrounding α-cell biology describing glucagon's primary role in glucose counterregulation to one where glucagon is critical in regulating both hyper- and hypoglycemic responses. Herein, this review will update the current understanding of the role of glucagon and α-cell-derived GLP-1, placing emphasis on their roles in regulating glucose homeostasis, insulin secretion, and β-cell mass.<br /> (© The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
- Subjects :
- Animals
Blood Glucose analysis
Diabetes Mellitus, Type 2 metabolism
Glucose metabolism
Homeostasis
Humans
Insulin metabolism
Mice
Pancreas metabolism
Glucagon metabolism
Glucagon-Like Peptide 1 metabolism
Glucagon-Secreting Cells metabolism
Insulin Secretion
Insulin-Secreting Cells metabolism
Proglucagon metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1945-7170
- Volume :
- 162
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Endocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 34318874
- Full Text :
- https://doi.org/10.1210/endocr/bqab150