Improved glucose tolerance in rats treated with the dipeptidyl peptidase IV (CD26) inhibitor Ile-thiazolidide-Reference-Cited by-同舟云学术

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Improved glucose tolerance in rats treated with the dipeptidyl peptidase IV (CD26) inhibitor Ile-thiazolidide

Published:1999-03 Issue:3 Volume:48 Page:385-389
ISSN:0026-0495
Container-title:Metabolism
language:en
Short-container-title:Metabolism

Author:

Pauly Robert P.,Demuth Hans-Ulrich,Rosche Fred,Schmidt Jörn,White Heather A.,Lynn Francis,McIntosh Christopher H.S.,Pederson Raymond A.

Publisher

Elsevier BV

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference23 articles.

1. Entero-insular axis;Unger;Arch Intern Med,1969

2. Cell and molecular biology of the incretin hormones glucagon-like peptide-1 and glucose-dependent insulin releasing polypeptide;Fehmann;Endocr Rev,1995

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

4. Degradation of glucose-dependent insulinotropic polypeptide and truncated glucagon-like peptide 1 in vitro and in vivo by dipeptidyl peptidase IV;Kieffer;Endocrinology,1995

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 Endocinol Metab,1995

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