Neurogenin 3-Specific Dipeptidyl Peptidase-2 Deficiency Causes Impaired Glucose Tolerance, Insulin Resistance, and Visceral Obesity

Author:

Danilova Olga V.1,Tai Albert K.1,Mele Deanna A.1,Beinborn Martin2,Leiter Andrew B.3,Greenberg Andrew S.4,Perfield James W.4,DeFuria Jason4,Singru Praful S.5,Lechan Ronald M.5,Huber Brigitte T.1

Affiliation:

1. Department of Pathology (O.V.D., A.K.T., D.A.M., B.T.H.), Tufts University School of Medicine, Boston, Massachusetts 02111

2. Molecular Cardiology Research Institute (M.B.), Molecular Pharmacology Research Center, Boston, Massachusetts 02111

3. Department of Medicine (A.B.L.), University of Massachusetts Medical School, Worcester, Massachusetts 01605

4. Department of Obesity and Metabolism (A.S.G., J.W.P., J.D.), Jean Mayer United States Department of Agriculture Human Nutrition Research Center on Aging at Tufts University, Boston, Massachusetts 02111

5. Tupper Research Institute and Department of Medicine (P.S.S., R.M.L.), Division of Endocrinology, Diabetes, and Metabolism, Tufts Medical Center, Boston, Massachusetts 02111

Publisher

The Endocrine Society

Subject

Endocrinology

Reference38 articles.

1. Brain-adipose tissue neural crosstalk.;Bartness;Physiol Behav,2007

2. Obesity: pathophysiology and clinical management.;Gurevich-Panigrahi;Curr Med Chem,2009

3. Glucagon-like peptide-1, but not glucose-dependent insulinotropic peptide, regulates fasting glycemia and nonenteral glucose clearance in mice.;Baggio;Endocrinology,2000

4. Dipeptidyl-peptidase IV hydrolyses gastric inhibitory polypeptide, glucagon-like peptide-1(7–36)amide, peptide histidine methionine and is responsible for their degradation in human serum.;Mentlein;Eur J Biochem,1993

5. Degradation of glucagon-like peptide-1 by human plasma in vitro yields an N-terminally truncated peptide that is a major endogenous metabolite in vivo.;Deacon;J Clin Endocrinol Metab,1995

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