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PMID: 12086940 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Adrenalectomy improves diabetes in A-ZIP/F-1 lipoatrophic mice by increasing both liver and muscle insulin sensitivity.

Diabetes ·Vol. 51 ·No. 7 ·2002-07-00 ·Pages 2113-8

Haluzik M, Dietz KR, Kim JK, Marcus-Samuels B, Shulman GI, Gavrilova O, Reitman ML

Abstract

The virtually fatless A-ZIP/F-1 mouse is profoundly insulin resistant, diabetic, and a good model for humans with severe generalized lipoatrophy. Like a number of other mouse models of diabetes, the A-ZIP/F-1 mouse has elevated serum corticosterone levels. Leptin infusion lowers the corticosterone levels, suggesting that leptin deficiency contributes to the hypercorticosteronemic state. To test the hypothesis that the increased glucocorticoids contribute to the diabetes and insulin resistance, we examined the effect of adrenalectomy on A-ZIP/F-1 mice. Adrenalectomy significantly decreased the blood glucose, serum insulin, and glycated hemoglobin levels. Hyperinsulinemic-euglycemic clamps were performed to characterize the changes in whole-body and tissue insulin sensitivity. The adrenalectomized A-ZIP/F-1 mice displayed a marked improvement in insulin-induced suppression of endogenous glucose production, indicating increased hepatic insulin sensitivity. Adrenalectomy also increased muscle glucose uptake and glycogen synthesis. These results suggest that the chronically increased serum corticosterone levels contribute to the diabetes of the A-ZIP/F-1 mice and that removal of the glucocorticoid excess improves the insulin sensitivity in both muscle and liver.

MeSH Terms
Adrenalectomy Animals Blood Glucose/metabolism Body Weight Diabetes Mellitus, Lipoatrophic/blood,metabolism,surgery Disease Models, Animal Energy Intake Fatty Acids, Nonesterified/blood Glucose Clamp Technique Glycated Hemoglobin A/metabolism Humans Insulin/pharmacology Liver/metabolism Mice Mice, Mutant Strains Mice, Transgenic Muscle, Skeletal/metabolism Organ Size Transcription Factors/genetics Triglycerides/blood,metabolism
Chemicals
Blood Glucose Fatty Acids, Nonesterified Glycated Hemoglobin A Insulin Tg(AZIP-F)1Vsn protein, mouse Transcription Factors Triglycerides
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Haluzik Martin
Diabetes Branch, National Institute of Diabetes and Digestive and Kidney Diseases/NIH, Building 10, Room 8N-250, 10 Center Drive, Bethesda, MD 20892-1770, USA. [email protected]
Dietz Kelly R
Kim Jason K
Marcus-Samuels Bernice
Shulman Gerald I
Gavrilova Oksana
Reitman Marc L
Article Info
Journal
Diabetes
Abbr.
Diabetes
ISSN
0012-1797
Published
2002-07-00
Pages
2113-8
Language
English
Region
United States
NLM ID
0372763
Subset
IM
Grants
NIDDK NIH HHS · R01 DK040936 · United States
NIDDK NIH HHS · R01 DK-40936 · United States
NIDDK NIH HHS · U24 DK-59635 · United States
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