نتایج جستجو برای: glucagon like peptide 1

تعداد نتایج: 3320018  

2013
Sarah H Lockie Aneta Stefanidis Brian J Oldfield Diego Perez-Tilve

The capacity for increased thermogenesis through brown adipose tissue (BAT) activation is important for body weight homeostasis. Differences in BAT thermogenesis can underlie significant differences in body weight and body composition, as we demonstrate in a rat model of obesity. This mini-review focuses on our current understanding of physiological BAT regulation, with a view to how it may be ...

2015
Aung Myat Satpal Arri Deepak L Bhatt Bernard J Gersh Simon R Redwood Michael S Marber

BACKGROUND Glucagon-like peptide-1 is an incretin hormone essential for normal human glucose homeostasis. Expression of the glucagon-like peptide-1 receptor in the myocardium has fuelled growing interest in the direct and indirect cardiovascular effects of native glucagon-like peptide-1, its degradation product glucagon-like peptide-1(9-36), and the synthetic glucagon-like peptide-1 receptor ag...

2010
Kristine J. Hare Tina Vilsbøll Meena Asmar Carolyn F. Deacon Filip K. Knop Jens J. Holst

OBJECTIVE Glucagon-like peptide 1 (GLP-1) exerts beneficial antidiabetic actions via effects on pancreatic beta- and alpha-cells. Previous studies have focused on the improvements in beta-cell function, while the inhibition of alpha-cell secretion has received less attention. The aim of this research was to quantify the glucagonostatic contribution to the glucose-lowering effect of GLP-1 infusi...

Journal: :Circulation. Heart failure 2014
Kenneth B Margulies Kevin J Anstrom Adrian F Hernandez Margaret M Redfield Monica R Shah Eugene Braunwald Thomas P Cappola

Journal: :Physiology 2005
Elaine M Sinclair Daniel J Drucker

Glucagon is used for the treatment of hypoglycemia, and glucagon receptor antagonists are under development for the treatment of type 2 diabetes. Moreover, glucagon-like peptide (GLP)-1 and GLP-2 receptor agonists appear to be promising therapies for the treatment of type 2 diabetes and intestinal disorders, respectively. This review discusses the physiological, pharmacological, and therapeutic...

Journal: :Diabetes care 2001
J Larsen B Hylleberg K Ng P Damsbo

OBJECTIVE To assess the efficacy and safety of glucagon-like peptide-1 (GLP-1) on the plasma glucose level when given as a continuous infusion for either 16 or 24 h per day to type 2 diabetic patients who were poorly controlled on sulfonylurea treatment. RESEARCH DESIGN AND METHODS This single-center, randomized, parallel, double-blind, placebo-controlled trial was conducted in 40 hospitalize...

2012
Ida Kinalska Dorota Bednarska-Chabowska Joanna Adamiec-Mroczek Łukasz Hak

The authors discuss the strategy of use of incretin hormones in type 2 diabetes treatment in the context of cardiovascular complications. The results of the phase III study on human GLP-1 (Glucagon-like peptide-1) analogue-liraglutide have been presented under common acronym LEAD (Liraglutide-Effect and Action In Diabetes). The liraglutide therapy improved glycemic control with low hypoglycemia...

2013
Marc Y. Donath Rémy Burcelin

According to the classical incretin concept, glucagon-like peptide (GLP)-1 is viewed as a hormone produced in the intestinal L cells and acting via the circulation on satiety in the brain, gut motility, and insulin and glucagon secretion in the pancreatic islet. However, in contrast to typical hormones, plasma levels of GLP-1 are relatively low with a very short half-life. Furthermore, GLP-1 is...

Journal: :Research in veterinary science 2015
I Padrutt T A Lutz C E Reusch E Zini

Incretin analogues and inhibitors of the breakdown of endogenous incretins are antidiabetic drugs that increase β-cell proliferation and glucose-stimulated insulin secretion in rodents and humans. Objectives were to test whether exenatide, exenatide extended-release, and sitagliptin can be safely used in cats, to identify the most effective drug, and to test the effects of prolonged exenatide e...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید