نتایج جستجو برای: dpp4

تعداد نتایج: 682  

Journal: :JAMA 2007
Darryl T Gray William Hollingworth Nneka Onwudiwe Richard A Deyo Jeffrey G Jarvik

finding that DPP4 enzymatic activity in nasal tissue biopsies taken from patients with chronic rhinosinusitis was inversely correlated with the density of inflammatory cells in the nasal mucosa, and the DPP4 activity increased when chronic sinusitis was treated. Dipeptidyl peptidase 4 inactivates the proinflammatory peptide substance P that is released by sensory nerve fibers of the nasal mucos...

2012
Aiying Wang Charles Dorso Lisa Kopcho Gregory Locke Robert Langish Eric Harstad Petia Shipkova Jovita Marcinkeviciene Lawrence Hamann Mark S Kirby

BACKGROUND Dipeptidylpeptidase 4 (DPP4) inhibitors have clinical benefit in patients with type 2 diabetes mellitus by increasing levels of glucose-lowering incretin hormones, such as glucagon-like peptide -1 (GLP-1), a peptide with a short half life that is secreted for approximately 1 hour following a meal. Since drugs with prolonged binding to their target have been shown to maximize pharmaco...

2010
Meghan Sauvé Kiwon Ban M. Abdul Momen Yu-Qing Zhou R. Mark Henkelman Mansoor Husain Daniel J. Drucker

OBJECTIVE Glucagon-like peptide-1 (7-36)amide (GLP-1) is cleaved by dipeptidyl peptidase-4 (DPP-4) to GLP-1 (9-36)amide. We examined whether chemical inhibition or genetic elimination of DPP-4 activity affects cardiovascular function in normoglycemic and diabetic mice after experimental myocardial infarction. RESEARCH DESIGN AND METHODS Cardiac structure and function was assessed by hemodynam...

Journal: :Cancer research 2006
Giulio Ghersi Qiang Zhao Monica Salamone Yunyun Yeh Stanley Zucker Wen-Tien Chen

Dipeptidyl peptidase IV (DPP4/CD26) and seprase/fibroblast activation protein alpha are homologous type II transmembrane, homodimeric glycoproteins that exhibit unique prolyl peptidase activities. Human DPP4 is ubiquitously expressed in epithelial and endothelial cells and serves multiple functions in cleaving the penultimate positioned prolyl bonds at the NH(2) terminus of a variety of physiol...

2015
Lesley Baerts Yannick Waumans Inger Brandt Wolfgang Jungraithmayr Pieter Van der Veken Marc Vanderheyden Ingrid De Meester Meijing Wang

BACKGROUND The chemokine Stromal cell-derived factor 1α (SDF1α, CXCL12) is currently under investigation as a biomarker for various cardiac diseases. The correct interpretation of SDF1α levels is complicated by the occurrence of truncated forms that possess an altered biological activity. METHODOLOGY We studied the immunoreactivities of SDF1α forms and evaluated the effect of adding a DPP4 in...

2014
Fan Yang Tianpeng Zheng Yun Gao Attit Baskota Tao Chen Xingwu Ran Haoming Tian

AIMS To determine whether fasting plasma Dipeptidyl Peptidase 4 (DPP4) activity and active Glucagon-Like Peptide-1 (GLP-1) were predictive of the onset of metabolic syndrome. METHODS A prospective cohort study was conducted of 2042 adults (863 men and 1,179 women) aged 18-70 years without metabolic syndrome examined in 2007(baseline) and 2011(follow-up). Baseline plasma DPP4 activity was dete...

2016
Jérémie Decalf Kristin V Tarbell Armanda Casrouge Jeffrey D Price Grace Linder Estelle Mottez Philippe Sultanik Vincent Mallet Stanislas Pol Darragh Duffy Matthew L Albert

Biochemical experiments, animal models, and observational studies in humans all support a role of dipeptidyl peptidase 4 (DPP4) in the N-terminal truncation of CXCL10, which results in the generation of an antagonist form of the chemokine that limits T-cell and NK cell migration. Motivated by the ability to regulate lymphocyte trafficking in vivo, we conducted two prospective clinical trials to...

Journal: :Diabetes 2016
Erin E Mulvihill Elodie M Varin John R Ussher Jonathan E Campbell K W Annie Bang Tahmid Abdullah Laurie L Baggio Daniel J Drucker

Dipeptidyl peptidase-4 (DPP4) inhibitors used for the treatment of type 2 diabetes are cardioprotective in preclinical studies; however, some cardiovascular outcome studies revealed increased hospitalization rates for heart failure (HF) among a subset of DPP4 inhibitor-treated subjects with diabetes. We evaluated cardiovascular function in young euglycemic Dpp4(-/-) mice and in older, high fat-...

2017
Santosh Gautam Abiy Agiro John Barron Thomas Power Harry Weisman Jeff White

BACKGROUND Newer oral antidiabetic drug classes are expanding treatment options for type 2 diabetes mellitus (T2DM); however, concerns remain. The objective was to assess relative risk of heart failure hospitalization of sodium-glucose co-transporter-2 (SGLT2) and dipeptidyl peptidase-4 (DPP4) inhibitors in T2DM patients. METHODS This retrospective observational study used a national commerci...

2014
Ravi Nistala Javad Habibi Annayya Aroor James R Sowers Melvin R Hayden Alex Meuth William Knight Tamara Hancock Thomas Klein Vincent G DeMarco Adam Whaley-Connell

OBJECTIVE Obesity-related glomerulopathy is characterized initially by glomerular hyperfiltration with hypertrophy and then development of proteinuria. Putative mechanisms include endothelial dysfunction and filtration barrier injury due to oxidant stress and immune activation. There has been recent interest in targeting dipeptidyl peptidase 4 (DPP4) enzyme due to increasing role in non-enzymat...

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