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
Main Authors: Wang, May-yun, Chen, Lijun, Clark, Gregory O, Lee, Young, Stevens, Robert D, Ilkayeva, Olga R, Wenner, Brett R, Bain, James R, Charron, Maureen J, Newgard, Christopher B, Unger, Roger H
Format: Journal Article
Language:English
Published: United States National Academy of Sciences 16-03-2010
National Acad Sciences
Series:Feature Article
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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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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