Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/11827
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dc.contributor.authorRodboon T.
dc.contributor.authorSirilun S.
dc.contributor.authorOkada S.
dc.contributor.authorKariya R.
dc.contributor.authorChontananarth T.
dc.contributor.authorSuwannalert P.
dc.date.accessioned2021-04-05T03:01:16Z-
dc.date.available2021-04-05T03:01:16Z-
dc.date.issued2020
dc.identifier.issn17355362
dc.identifier.other2-s2.0-85095132431
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/11827-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85095132431&doi=10.4103%2f1735-5362.297852&partnerID=40&md5=d820f1f1c02cb26be6b8470e1ea1cb93
dc.description.abstractExcessive melanin production caused by overactive tyrosinase (TYR) enzyme results in several dermatological problems. The TYR inhibitor, derived from metabolite changes during fermentation, has been well recognized for pigmentation control. Experimental approach: This study is interested in alternative anti-melanogenic agents from bio-modified Riceberry rice through fermentation. Modified Riceberry rice extract (MRB) was evaluated for its cytotoxicity, melanin content, melanin excretion, and TYR activity in B16 cells. TYR and their melanogenesis-related molecules such as TYR-related proteins-1 and -2, and microphthalmia-associated transcription factor (MITF) were determined. The anti-melanogenic activity and toxicity were also tested using the embryonic zebrafish model. Furthermore, comprehensive genotoxicity testing was verified by cytokinesis-block micronucleus cytome assay. Findings/Results: The study found that non-cytotoxic concentrations of MRB at 20 and 40 mg/mL inhibited melanogenesis and melanin excretion by interfering B16 cell morphology. Cellular TYR enzymatic activity was also suppressed in the treated cells. The mRNA transcription and protein expression levels of TYR and MITF decreased by dose-dependent and time-dependent manners with MRB treatment. In the animal model, MRB was found to be safe and potent for melanogenesis-related TYR inhibition in embryonic zebrafish at 20 and 30 mg/mL. The toxicity of effective doses of MRB showed no genotoxicity and mutagenicity. Conclusion and implications: This study suggests that MRB has anti-melanogenesis potential through TYR and its-related protein inhibitions. MRB is also safe for applications and maybe a promising anti-melanogenic agent for hyperpigmentation control. © 2020 Wolters Kluwer Medknow Publications. All rights reserved.
dc.subjectdopachrome tautomerase
dc.subjectmelanin
dc.subjectmicrophthalmia associated transcription factor
dc.subjectmodified Riceberry rice extract
dc.subjectmonophenol monooxygenase
dc.subjectoxygenase inhibitor
dc.subjectphenylthiourea
dc.subjectplant extract
dc.subjecttyrosinase related protein 1
dc.subjectunclassified drug
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantimelanogenic activity
dc.subjectArticle
dc.subjectB16 cell line
dc.subjectcell differentiation
dc.subjectcell structure
dc.subjectcontrolled study
dc.subjectcytokinesis
dc.subjectcytotoxicity
dc.subjectdown regulation
dc.subjectdrug activity
dc.subjectembryo
dc.subjectenzyme activity
dc.subjectenzyme inhibition
dc.subjectfemale
dc.subjectfermentation
dc.subjectgenotoxicity
dc.subjectgermination
dc.subjecthyperpigmentation
dc.subjectin vivo study
dc.subjectmale
dc.subjectmelanogenesis
dc.subjectmicronucleus test
dc.subjectmRNA expression level
dc.subjectmutagenic activity
dc.subjectmutagenicity
dc.subjectnonhuman
dc.subjectprotein expression
dc.subjectprotein expression level
dc.subjectrice
dc.subjectRiceberry rice
dc.subjectSaccharomyces cerevisiae
dc.subjectzebra fish
dc.titleModified Riceberry rice extract suppresses melanogenesis-associated cell differentiation through tyrosinase-mediated MITF downregulation on B16 cells and in vivo zebrafish embryos
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationResearch in Pharmaceutical Sciences. Vol 15, No.5 (2020), p.491-502
dc.identifier.doi10.4103/1735-5362.297852
Appears in Collections:Scopus 1983-2021

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