Literature DB >> 19343230

Liraglutide: a new treatment for type 2 diabetes.

Tina Vilsboll1.   

Abstract

Liraglutide is a novel glucagon-like peptide-1 (GLP-1) receptor agonist with 97% amino acid sequence identity to native GLP-1. An amino acid substitution and fatty acid side chain enable a more protracted pharmacokinetic profile of over 24 hours. These modifications make liraglutide suitable for once-daily dosing. Liraglutide use exploits the incretin effect to glucose-dependently stimulate insulin secretion. The LEAD (Liraglutide Effect and Action Diabetes) program evaluated the safety and efficacy of liraglutide and demonstrated an improved level of glycemic control relative to currently used oral antidiabetic drugs, including other GLP-1-based therapies. In these trials, liraglutide was shown to enable many patients to achieve hemoglobin A1c (HbA1c) targets and to improve several morbidities commonly associated with type 2 diabetes; liraglutide induced weight loss, reduced systolic blood pressure and improved beta-cell function. Liraglutide was well tolerated, although an increased incidence of mild nausea was observed. Since liraglutide mimics the glucose-sensitive action of native GLP-1, it does not induce hypoglycemia. Liraglutide offers an interesting alternative therapy to control blood glucose levels in patients with type 2 diabetes, who commonly present with hypertension and overweight. It is expected to be approved by the U.S. Food and Drug Administration and the European Medicines Agency in Europe for use in 2009. Copyright 2009 Prous Science, S.A.U. or its licensors. All rights reserved.

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Year:  2009        PMID: 19343230     DOI: 10.1358/dot.2009.45.2.1336104

Source DB:  PubMed          Journal:  Drugs Today (Barc)        ISSN: 1699-3993            Impact factor:   2.245


  11 in total

Review 1.  The contribution of enteroinsular hormones to the pathogenesis of type 2 diabetes mellitus.

Authors:  Dima L Diab; David A D'Alessio
Journal:  Curr Diab Rep       Date:  2010-06       Impact factor: 4.810

2.  Expression and distribution of glucagon-like peptide-1 receptor mRNA, protein and binding in the male nonhuman primate (Macaca mulatta) brain.

Authors:  Kristy M Heppner; Melissa Kirigiti; Anna Secher; Sarah Juel Paulsen; Rikley Buckingham; Charles Pyke; Lotte B Knudsen; Niels Vrang; Kevin L Grove
Journal:  Endocrinology       Date:  2015-01       Impact factor: 4.736

Review 3.  Glucagon-like peptide-1 analogues for Type 2 diabetes mellitus: current and emerging agents.

Authors:  Baptist Gallwitz
Journal:  Drugs       Date:  2011-09-10       Impact factor: 9.546

Review 4.  The evolving place of incretin-based therapies in type 2 diabetes.

Authors:  Baptist Gallwitz
Journal:  Pediatr Nephrol       Date:  2010-02-04       Impact factor: 3.714

Review 5.  What are the risks and the benefits of current and emerging weight-loss medications?

Authors:  Jamie R Robinson; Kevin D Niswender
Journal:  Curr Diab Rep       Date:  2009-10       Impact factor: 4.810

6.  Drugs developed to treat diabetes, liraglutide and lixisenatide, cross the blood brain barrier and enhance neurogenesis.

Authors:  Kerry Hunter; Christian Hölscher
Journal:  BMC Neurosci       Date:  2012-03-23       Impact factor: 3.288

7.  Liraglutide improves hypertension and metabolic perturbation in a rat model of polycystic ovarian syndrome.

Authors:  Vanessa Hoang; Jiangjiang Bi; Sheba M Mohankumar; Arpita K Vyas
Journal:  PLoS One       Date:  2015-05-26       Impact factor: 3.240

8.  Liraglutide Activates the Nrf2/HO-1 Antioxidant Pathway and Protects Brain Nerve Cells against Cerebral Ischemia in Diabetic Rats.

Authors:  Caihong Deng; Jun Cao; Jiangquan Han; Jianguo Li; Zhaohun Li; Ninghua Shi; Jing He
Journal:  Comput Intell Neurosci       Date:  2018-02-12

Review 9.  Automated solid-phase peptide synthesis to obtain therapeutic peptides.

Authors:  Veronika Mäde; Sylvia Els-Heindl; Annette G Beck-Sickinger
Journal:  Beilstein J Org Chem       Date:  2014-05-22       Impact factor: 2.883

10.  Treatment With Liraglutide Exerts Neuroprotection After Hypoxic-Ischemic Brain Injury in Neonatal Rats via the PI3K/AKT/GSK3β Pathway.

Authors:  Shan-Shan Zeng; Jun-Jie Bai; Huai Jiang; Jin-Jin Zhu; Chang-Chang Fu; Min-Zhi He; Jiang-Hu Zhu; Shang-Qin Chen; Pei-Jun Li; Xiao-Qin Fu; Zhen-Lang Lin
Journal:  Front Cell Neurosci       Date:  2020-01-30       Impact factor: 5.505

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