Reversal of Defective Glucagon Responses to Hypoglycemia in Insulin-dependent Autoimmune Diabetic Bb Rats.
From: Pacific Northwest Research Institute, 720 Broadway, Seattle, WA 98122, USA.
Endocrinology
- Publish Date: Jun 2007
- ISSN: 0013-7227
- Volume: 148
- Issue: 6
- Pages: 2863-9
- Medium: Print
- Language: English
- Citation (JAMA): Zhou Huarong, Zhang Tao, Oseid Elizabeth, et al. Reversal of Defective Glucagon Responses to Hypoglycemia in Insulin-dependent Autoimmune Diabetic Bb Rats.. Endocrinology Jun 2007;148:2863-9
Abstract
The intraislet insulin hypothesis has been proposed to explain absent glucagon responses to hypoglycemia. Recently we directly confirmed this hypothesis by restoring glucagon secretion via provision of a pancreatic artery insulin infusion, which was switched off at the time of hypoglycemia in Wistar rats made diabetic by streptozotocin. The current study examined this hypothesis in a model of spontaneous, autoimmune diabetes, the insulin-dependent diabetic BB rat. The insulin switch-off signal restored the defective glucagon responses to hypoglycemia. However, the magnitude of the restored response was markedly less than that observed in control nondiabetic BB rats (4- to 5-month-old diabetic BB rats = 147 +/- 27; 2-month-old nondiabetic BB rats = 1038 +/- 112 pg/ml, peak delta; P < 0.0001). Because time was required for the BB rat to spontaneously develop diabetes, we asked whether the incomplete restoration of the glucagon response might be related to the animals’ growth and development. This led us to compare the glucagon response to hypoglycemia in nondiabetic BB and Wistar rats at 2 and 4-5 months of age. We observed age-related deterioration of not only glucose tolerance and insulin sensitivity but also glucagon responses to hypoglycemia in both strains. There was no significant difference between the glucagon responses to hypoglycemia in age-matched nondiabetic BB rats and diabetic BB rats provided with the insulin switch-off signal. We conclude that defective glucagon responses to hypoglycemia in BB rats can be corrected by restoring regulation of alpha-cell function by insulin.
Mesh Headings (Keywords): Animals, Blood Glucose, C-Peptide, Diabetes Mellitus, Type 1, Glucagon, Hypoglycemia, Insulin, Male, Rats, Rats, Inbred BB, Rats, Wistar
Check for Full Text / PubMed Unique Identifier (PMID): 17347310
This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.
Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.
The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.
