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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Ohishi, Takahide Yoshida, Shigeru |
| Description | Country affiliation: Japan Author Affiliation: Ohishi T ( Drug Discovery Research , Astellas Pharma Inc., 21 Miyukigaoka, Tsukuba, Ibaraki, Japan. takahide.ohishi@astellas.com) |
| Abstract | INTRODUCTION: Patients with type 2 diabetes mellitus (T2DM) are reaching an explosive number. Pancreatic ß cell dysfunction is the characteristic feature of the progression of T2DM and there is an increasing need for agents to improve its function. GPR119 is a G protein-coupled receptor (GPCR) expressed both in pancreatic ß cells and enteroendocrine cells and has garnered significant interest as a promising target for the next generation of T2DM drug. In vitro studies indicate that GPR119 agonists increase intracellular cAMP levels leading to enhanced glucose-induced insulin release and enhanced incretin hormone glucagon-like peptide 1 (GLP-1) secretion. In T2DM rodent models, GPR119 agonists are shown to decrease blood glucose level and preserve pancreatic ß cell function. AREAS COVERED: This review summarizes the function of GPR119 and the progresses made in the discovery of GPR119 agonists reported since 2002 in literatures. The importance of GPR119 agonists in glycemic control is discussed. EXPERT OPINION: GPR119 agonists with glucose-dependent insulin release and increased insulin promoter activity is expected to preserve pancreatic ß cell function, thereby providing great clinical benefits for T2DM patients. Both the preclinical and clinical data suggest that GPR119 agonist will be a promising anti-diabetic drug. |
| File Format | HTM / HTML |
| ISSN | 13543784 |
| Issue Number | 3 |
| Volume Number | 21 |
| e-ISSN | 17447658 |
| Journal | Expert Opinion on Investigational Drugs |
| Language | English |
| Publisher | Taylor & Francis |
| Publisher Date | 2012-03-01 |
| Publisher Place | Great Britain (UK) |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Discipline Analytical Chemistry Discipline Pharmacology Diabetes Mellitus, Type 2 Drug Therapy Hypoglycemic Agents Therapeutic Use Receptors, G-protein-coupled Agonists Animals Blood Glucose Drug Effects Diabetes Mellitus, Experimental Physiopathology Disease Progression Drug Delivery Systems Drug Design Humans Pharmacology Insulin-secreting Cells Pathology Metabolism Journal Article Review |
| Content Type | Text |
| Resource Type | Article |
| Subject | Pharmacology Pharmacology (medical) |
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