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dc.contributor.authorHossein Aarabi, Mohammad-
dc.contributor.authorMehdi Mirhashemi, Seyyed-
dc.date.accessioned2022-11-18T06:49:51Z-
dc.date.available2022-11-18T06:49:51Z-
dc.date.issued2017-09-10-
dc.identifier.citationAarabi, M. H., & Mirhashemi, S. M. (2017). To estimate effective antiamyloidogenic property of melatonin and fisetin and their actions to destabilize amyloid fibrils. Pak J Pharm Sci, 30(5), 1589-1593.en_US
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/14070-
dc.description.abstractAggregating of amylin as pancreatic deposition is connected with pancreas degeneration in type 2 diabetes mellitus. Suppression of the amylin accumulation and so instability of the pre-formed pancreatic β-amyloid, may be attractive curative goal for mediation of diabetes mellitus. Fluorimetric assay by Thioflavin-T was utilized for investigating the properties of melatonin and fisetin on the generation and instability of β-amyloid near to physiological conditions. The results showed that after 168 hours incubation by shaker incubator in 37o C, melatonin at 10µM and 40 µM repressed amylin amyloid formation by 20.1% and 27.5% respectively (p<0.05) and the similar values of fisetin inhibited the formation of β-sheet structure by 16.5% and 23.2% respectively (p<0.05).The obtained data also confirmed that amyloidal sheet opening was induced by elatonin and fisetin significantly (p<0.05). It may be concluded that islet amyloid cytotoxicity to β-cells may be reduced by melatonin and fisetin, and they should be important constituents of new drugs for diabetes mellitus reatment.en_US
dc.language.isoenen_US
dc.publisherKarachi: Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachien_US
dc.subjectAmylinen_US
dc.subjectDiabetes Mellitusen_US
dc.subjectMelatoninen_US
dc.subjectFisetinen_US
dc.subjectAmylin fibrilsen_US
dc.titleTo estimate effective antiamyloidogenic property of melatonin and fisetin and their actions to destabilize amyloid fibrilsen_US
dc.typeArticleen_US
Appears in Collections:No.5 September, 2017

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