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dc.contributor.advisorTahsin, Faria
dc.contributor.authorMahmood, Nyrit
dc.date.accessioned2021-10-25T05:31:51Z
dc.date.available2021-10-25T05:31:51Z
dc.date.copyright2021
dc.date.issued2021-05
dc.identifier.otherID 17146013
dc.identifier.urihttp://hdl.handle.net/10361/15532
dc.descriptionThis thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2021.en_US
dc.descriptionCataloged from PDF version of thesis report.
dc.descriptionIncludes bibliographical references (pages 35-41).
dc.description.abstractApproximately 422 million people have diabetes all over the world. The regeneration of the beta cell has been investigated for a longer time by scientists with the hope of newer potential opportunities, thus contributing to the treatment of diabetes. Beta-cell regeneration is a mechanism of producing new beta cells in the pancreas, which is responsible for the secretion of insulin, currently on pre-clinical trials. In this study, the action of each three receptors – GLP-1, DPP-4, and DYRK1A has been discussed. Their possibility of combination in the regeneration of damaged beta cells for the welfare of diabetic patients by comparing the ability of each of the receptors to regenerate beta cells as well as the combination of actions on these receptors produce any better effect or not has also been analyzed. However, millions of people with diabetes have a ray of hope as the current use of GLP-1 and DYRK1A indicates a prospective technique based on DYRK1A inhibition with the GLP-1 receptor. Moreover, it is also a fact that still there is no evidence of any potential combined treatment with the use of GLP-1 and DPP-4 for diabetic patients.en_US
dc.description.statementofresponsibilityNyrit Mahmood
dc.format.extent41 pages
dc.language.isoenen_US
dc.publisherBrac Universityen_US
dc.rightsBrac University theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission.
dc.subjectDipeptidyl peptidase-4en_US
dc.subjectDual specificity tyrosine-phosphorylation-regulated kinase 1Aen_US
dc.subjectBeta-cell regenerationen_US
dc.subjectDiabetesen_US
dc.subject.lcshGlucagon-like peptide 1
dc.subject.lcshDiabetes--Oral therapy
dc.titleA review on insulin-producing beta cell: regenerative role of drugs acting on DYRK1A, GLP-1 and DPP-4 receptorsen_US
dc.typeThesisen_US
dc.contributor.departmentDepartment of Pharmacy, Brac University
dc.description.degreeB. Pharmacy


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