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Glucose Stimulates and Potentiates Islet Amyloid Polypeptide Secretion by the B-Cell
Abstract
Islet amyloid polypeptide (IAPP) has been shown to be actively secreted by the pancreatic B-cell along with insulin. To determine whether the modulation of B-cell IAPP secretion is similar to that of insulin, we assessed IAPP release in response to glucose at 4 different concentrations (1.67, 5.5, 8.8 and 16.7 mM) and to non-glucose secretagogues at different glucose concentrations in a neonatal rat islet monolayer culture preparation. Glucose alone stimulated IAPP and insulin secretion in a dose dependent fashion with maximal release for both peptides occurring at 8.8 mM. B-cell secretion of IAPP in response to arginine, isobutylmethylxanthine or both together was potentiated by increasing glucose concentrations from 1.67 to 16.7 mM. This same pattern of glucose potentiation was observed for insulin secretion. The data indicate that the pattern of peptide responses of cultured neonatal B-cells to glucose is similar for both IAPP and insulin release. Furthermore, the data suggest that glucose is capable of potentiating B-cell secretion of both IAPP and insulin.
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IAPP is co-localized within the same secretory granules as insulin and is typically co-released with insulin in vitro in response to glucose and non-glucose secretagogues.
“IAPP is co-localized within the same secretory granules as insulin [115] and is typically co-released with insulin in vitro in response to glucose and non-glucose secretagogues [116, 117].”
From The relative contributions of insulin resistance and beta-cell dysfunction to the pathophysiology of type 2 diabetes (2003) · cites this paper as [117]
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Kahn, S. E. (2003) · Diabetologia · doi:10.1007/s00125-002-1009-0 · Cited by 2,166
Self-citationIslet Amyloid Polypeptide, Islet Amyloid, and Diabetes Mellitus
Westermark, P., Andersson, A., & Westermark, G. T. (2011) · Physiological Reviews · doi:10.1152/physrev.00042.2009 · Cited by 1,044
Kahn, S. E., Verchere, C. B., Andrikopoulos, S., Asberry, P. J., Leonetti, D. L., Wahl, P. W., Boyko, E. J., Schwartz, R. S., Newell-Morris, L., & Fujimoto, W. Y. (1998) · Diabetes · doi:10.2337/diabetes.47.4.640 · Cited by 74
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Metadata
- Authors
- Kahn, S., Fujimoto, W., D'Alessio, D., Ensinck, J., & Porte, D.
- Affiliations
- University of Washington (US)
- ORCID
- Kahn, S.
- Venue
- Hormone and Metabolic Research
- Publisher
- Georg Thieme Verlag KG
- Published
- 1991-12
- Volume
- 23
- Issue
- 12
- Pages
- 577-580
- ISSN
- 0018-5043 (ISSN-L)
- 1439-4286
- OpenAlex
- W2087179097
- Cited by
- 28
- References
- 0
- Citations by year
- 2024: 1 · 2021: 1 · 2020: 1 · 2018: 2 · 2015: 1 · 2014: 1
- FWCI
- 2.42
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Hormone and Metabolic Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Veterans Affairs
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 02456, DK07247, DK-03497, T32DK007247)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pancreatic function and diabetes
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
- Keywords
- amylin, insulin, pancreatic beta cells, glucose stimulation, L-arginine, 3-isobutyl-1-methylxanthine
- MeSH terms
- Insulin Secretion, Amyloid, Animals, Arginine, Cells, Cultured, Drug Synergism, Glucose, Insulin, Islets of Langerhans, Rats, Inbred Strains, 1-Methyl-3-isobutylxanthine, Rats, Islet Amyloid Polypeptide
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