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dc.contributor.authorRomteera Kittichaiworakulen_US
dc.contributor.authorSirinya Tayaen_US
dc.contributor.authorArpamas Chariyakornkulen_US
dc.contributor.authorThanongsak Chaiyasoen_US
dc.contributor.authorRawiwan Wongpoomchaien_US
dc.date.accessioned2022-10-16T07:01:47Z-
dc.date.available2022-10-16T07:01:47Z-
dc.date.issued2021-05-01en_US
dc.identifier.issn2218273Xen_US
dc.identifier.other2-s2.0-85105743716en_US
dc.identifier.other10.3390/biom11050734en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85105743716&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/75667-
dc.description.abstractRed yeast (Sporidiobolus pararoseus), obtained from glycerol waste in the biodiesel process, has been used as a mycotoxin sorbent in some agricultural products. This study focused on the antigenotoxic effects of red yeast on aflatoxin B1 (AFB1)‐induced mutagenesis, using a Salmonella mutation assay and a rat liver micronucleus test. Red yeast was sequentially extracted to obtain hexane, acetone, hot water, and residue fractions. Carbohydrates were mainly found in hot water extract (HWE), while proteins were observed in the residue fraction. The amount of lycopene in hexane extract (HE) was higher than the amount of β‐carotene in HE. All red yeast extracts were not mutagenic in the Salmonella typhimurium strains TA98 and TA100 under the presence and absence of metabolic activation. Among the extracts obtained from red yeast, HE presented the strongest antimutagenicity against AFB1‐induced mutagenesis in both strains, but HWE did not show any antimutagenicity. The oral administration of red yeast, HE, and HWE for 28 days was further investigated in rats. These extracts did not induce micronucleated hepatocytes. Furthermore, they modulated the activities of some detoxifying enzymes but did not alter the activities of various cy-tochrome P450 isozymes. Notably, they significantly decreased hepatic micronucleus formation in AFB1‐initiated rats. HE altered the activity of hepatic glutathione‐S‐transferase but did not affect its protein expression. Taken together, the antigenotoxicity of red yeast against AFB1‐induced muta-genesis might be partly due to the modulation of some detoxifying enzymes in AFB1 metabolism. β‐Carotene and lycopene might be promising antigenotoxic compounds in red yeast.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleAntigenotoxic effects and possible mechanism of red yeast (Sporidiobolus pararoseus) on aflatoxin b1‐induced mutagenesisen_US
dc.typeJournalen_US
article.title.sourcetitleBiomoleculesen_US
article.volume11en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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