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dc.contributor.authorÇolak R.
dc.date.accessioned2020-06-21T09:36:29Z
dc.date.available2020-06-21T09:36:29Z
dc.date.issued2012
dc.identifier.issn1300-2996
dc.identifier.urihttps://doi.org/10.5835/jecm.omu.29.s1.007
dc.identifier.urihttps://hdl.handle.net/20.500.12712/4427
dc.description.abstractIncretin hormones are defined as intestinal hormones released in response to nutrient ingestion. The incretin hormones include glucagon-like peptide (GLP-l) and glucose dependent polypeptide (GIP). GLP-l secreted by L cells from ileum and colon while GIP is maily produced K cells from the upper small intestine. Incretin hormones potentiate the glucose induced insulin response from pancreatic beta cells. With their non weight-gain, non hypoglycemic attributes and with positive effects on beta cell mass and lifetime as proven by animal experiments, parenterally used GLP-1 agonists of Exenatide and Liraglutide have emerged among medications used for the treatment of early stage diabetes. Dipeptidyl peptidase-4 inhibitors are effective either as a single or combination therapy in lowering glycated hemoglobin, fasting and postprandial glucose levels, with a low incidence of hypoglycemia and no weight gain. © 2012 OMU.en_US
dc.language.isoturen_US
dc.publisherOndokuz Mayis Universitesien_US
dc.relation.isversionof10.5835/jecm.omu.29.s1.007en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDiabetes mellitusen_US
dc.subjectDPP-4 inhibitorsen_US
dc.subjectExenatideen_US
dc.subjectGLP-1 analoguesen_US
dc.subjectIncretinsen_US
dc.subjectLiraglutideen_US
dc.titleIncretins in the treatment of type 2 diabetes mellitusen_US
dc.title.alternativeTip 2 diabetes mellitus tedavisinde inkretinleren_US
dc.typereviewen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume29en_US
dc.identifier.startpage30en_US
dc.identifier.endpage38en_US
dc.relation.journalOndokuz Mayis Universitesi Tip Dergisien_US
dc.relation.publicationcategoryDiğeren_US


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