Leptin therapy in insulin-deficient type I diabetes
In nonobese diabetic mice with uncontrolled type 1 diabetes, leptin therapy alone or combined with low-dose insulin reverses the catabolic state through suppression of hyperglucagonemia. Additionally, it mimics the anabolic actions of insulin monotherapy and normalizes hemoglobin A1c with far less g...
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Published in: | Proceedings of the National Academy of Sciences - PNAS Vol. 107; no. 11; pp. 4813 - 4819 |
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Main Authors: | , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
National Academy of Sciences
16-03-2010
National Acad Sciences |
Series: | Feature Article |
Subjects: | |
Online Access: | Get full text |
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Summary: | In nonobese diabetic mice with uncontrolled type 1 diabetes, leptin therapy alone or combined with low-dose insulin reverses the catabolic state through suppression of hyperglucagonemia. Additionally, it mimics the anabolic actions of insulin monotherapy and normalizes hemoglobin A1c with far less glucose variability. We show that leptin therapy, like insulin, normalizes the levels of a wide array of hepatic intermediary metabolites in multiple chemical classes, including acylcarnitines, organic acids (tricarboxylic acid cycle intermediates), amino acids, and acyl CoAs. In contrast to insulin monotherapy, however, leptin lowers both lipogenic and cholesterologenic transcription factors and enzymes and reduces plasma and tissue lipids. The results imply that leptin administration may have multiple short- and long-term advantages over insulin monotherapy for type 1 diabetes. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Author contributions: R.H.U. designed research; M.-y.W., L.C., R.D.S., O.R.I., B.R.W., J.R.B., and C.B.N. performed research; M.C. provided mice; C.B.N. contributed analytic tools; M.-y.W., YL., L.C., G.O.C., R.D.S., O.R.I., B.R.W., J.R.B., C.B.N., and R.H.U. analyzed data; and R.H.U. wrote the paper. Edited by Jeffrey M. Friedman, Howard Hughes Medical Institute/Rockefeller University, New York, NY, and approved January 12, 2010 (received for review October 7, 2009) |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.0909422107 |