Title | Contemporary Updates on the Physiology of Glucagon like Peptide-1 and Its Agonist to Treat Type 2 Diabetes Mellitus |
Publication Type | Journal Article |
Year of Publication | 2020 |
Authors | Anju, D., K. M. Geetha, and H. Iswar |
Journal | International Journal of Peptide Research and Therapeutics |
Volume | 26 |
Issue | 3 |
Pagination | 1211 - 1221 |
Date Published | 2020 |
Type of Article | Review |
ISBN Number | 15733149 (ISSN) |
Keywords | College of Pharmaceutical Sciences, Scopus, WoS |
Abstract | Pathogenesis of diabetes mellitus involves scores of different factors, out of which Glucagon like factor-1 (GLP-1) plays a foremost role. GLP-1 is a peptide-hormone of the incretin system. It exhibits glucagonostatic as well as glucose dependent insulinotropic action. GLP-1 augments regeneration of β-cell, boost secretion of insulin and trim down weight gain in type-2 diabetes. GLP-1 discharge from the L cells of intestine is mediated by neural and hormonal factors which are stimulated by the occurrence of nutrients in the gastrointestinal tract. Conversely, GLP-1 is instantaneously shattered by enzyme dipeptidyl peptidase-IV. GLP-1 is also cleared by renal clearance. Diminished GLP-1 leads to attenuated insulin release leading to type-2 diabetes. Substitution of GLP-1 regularizes the insulin release and prevents type-2 diabetes. However, GLP-1 holding infinitesimal plasma half life limits its therapeutic effects. To surmount the limitations of indigenous GLP-1, several GLP-1 receptor agonist like Exenatide are been developed. Modifications in pharmaceutical formulation are also been made to meet the patients adherence to the medication of GLP-1 agonist. Graphic Abstract: [Figure not available: see fulltext.] © 2019, Springer Nature B.V. |
URL | https://link.springer.com/article/10.1007%2Fs10989-019-09927-y |
DOI | 10.1007/s10989-019-09927-y |
Short Title | Int. J. Pept. Res. Ther. |