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Inhibitory effect of purple rice husk extract on AFB(1)-induced micronucleus formation in rat liver through modulation of xenobiotic metabolizing enzymes
BACKGROUND: Rice husk, a waste material produced during milling, contains numerous phytochemicals that may be sources of cancer chemopreventive agents. Various biological activities of white and colored rice husk have been reported. However, there are few comparative studies of the cancer chemopreve...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6724366/ https://www.ncbi.nlm.nih.gov/pubmed/31481128 http://dx.doi.org/10.1186/s12906-019-2647-9 |
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author | Chariyakornkul, Arpamas Punvittayagul, Charatda Taya, Sirinya Wongpoomchai, Rawiwan |
author_facet | Chariyakornkul, Arpamas Punvittayagul, Charatda Taya, Sirinya Wongpoomchai, Rawiwan |
author_sort | Chariyakornkul, Arpamas |
collection | PubMed |
description | BACKGROUND: Rice husk, a waste material produced during milling, contains numerous phytochemicals that may be sources of cancer chemopreventive agents. Various biological activities of white and colored rice husk have been reported. However, there are few comparative studies of the cancer chemopreventive effects of white and colored rice husk. METHODS: This study investigated the cancer chemopreventive activities of two different colors of rice husk using in vitro and in vivo models. A bacterial mutation assay using Salmonella typhimurium strains TA98 and TA100 was performed; enzyme induction activity in murine hepatoma cells was measured, and a liver micronucleus test was performed in male Wistar rats. RESULTS: The white rice husk (WRHE) and purple rice husk (PRHE) extracts were not mutagenic in Salmonella typhimurium TA98 or TA100 in the presence or absence of metabolic activation. However, the extracts exhibited antimutagenicity against aflatoxin B(1) (AFB(1)) and 2-amino-3,4 dimethylimidazo[4,5-f]quinolone (MeIQ) in a Salmonella mutation assay. The extracts also induced anticarcinogenic enzyme activity in a murine Hepa1c1c7 hepatoma cell line. Interestingly, PRHE but not WRHE exhibited antigenotoxicity in the rat liver micronucleus test. PRHE significantly decreased the number of micronucleated hepatocytes in AFB(1)-initiated rats. PRHE contained higher amounts of phenolic compounds and vitamin E than WRHE in both tocopherols and tocotrienols as well as polyphenol such as cyanidin-3-glucoside, protocatechuic acid and vanillic acid. Furthermore, PRHE increased CYP1A1 and 1A2 activities while decreasing CYP3A2 activity in the livers of AFB(1)-treated rats. PRHE also enhanced various detoxifying enzyme activities, including glutathione S-transferase, NAD(P)H quinone oxidoreductase and heme oxygenase. CONCLUSIONS: PRHE showed potent cancer chemopreventive activity in a rat liver micronucleus assay through modulation of phase I and II xenobiotic metabolizing enzymes involved in AFB(1) metabolism. Vitamin E and phenolic compounds may be candidate antimutagens in purple rice husk. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12906-019-2647-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6724366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67243662019-09-10 Inhibitory effect of purple rice husk extract on AFB(1)-induced micronucleus formation in rat liver through modulation of xenobiotic metabolizing enzymes Chariyakornkul, Arpamas Punvittayagul, Charatda Taya, Sirinya Wongpoomchai, Rawiwan BMC Complement Altern Med Research Article BACKGROUND: Rice husk, a waste material produced during milling, contains numerous phytochemicals that may be sources of cancer chemopreventive agents. Various biological activities of white and colored rice husk have been reported. However, there are few comparative studies of the cancer chemopreventive effects of white and colored rice husk. METHODS: This study investigated the cancer chemopreventive activities of two different colors of rice husk using in vitro and in vivo models. A bacterial mutation assay using Salmonella typhimurium strains TA98 and TA100 was performed; enzyme induction activity in murine hepatoma cells was measured, and a liver micronucleus test was performed in male Wistar rats. RESULTS: The white rice husk (WRHE) and purple rice husk (PRHE) extracts were not mutagenic in Salmonella typhimurium TA98 or TA100 in the presence or absence of metabolic activation. However, the extracts exhibited antimutagenicity against aflatoxin B(1) (AFB(1)) and 2-amino-3,4 dimethylimidazo[4,5-f]quinolone (MeIQ) in a Salmonella mutation assay. The extracts also induced anticarcinogenic enzyme activity in a murine Hepa1c1c7 hepatoma cell line. Interestingly, PRHE but not WRHE exhibited antigenotoxicity in the rat liver micronucleus test. PRHE significantly decreased the number of micronucleated hepatocytes in AFB(1)-initiated rats. PRHE contained higher amounts of phenolic compounds and vitamin E than WRHE in both tocopherols and tocotrienols as well as polyphenol such as cyanidin-3-glucoside, protocatechuic acid and vanillic acid. Furthermore, PRHE increased CYP1A1 and 1A2 activities while decreasing CYP3A2 activity in the livers of AFB(1)-treated rats. PRHE also enhanced various detoxifying enzyme activities, including glutathione S-transferase, NAD(P)H quinone oxidoreductase and heme oxygenase. CONCLUSIONS: PRHE showed potent cancer chemopreventive activity in a rat liver micronucleus assay through modulation of phase I and II xenobiotic metabolizing enzymes involved in AFB(1) metabolism. Vitamin E and phenolic compounds may be candidate antimutagens in purple rice husk. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12906-019-2647-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-09-03 /pmc/articles/PMC6724366/ /pubmed/31481128 http://dx.doi.org/10.1186/s12906-019-2647-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Chariyakornkul, Arpamas Punvittayagul, Charatda Taya, Sirinya Wongpoomchai, Rawiwan Inhibitory effect of purple rice husk extract on AFB(1)-induced micronucleus formation in rat liver through modulation of xenobiotic metabolizing enzymes |
title | Inhibitory effect of purple rice husk extract on AFB(1)-induced micronucleus formation in rat liver through modulation of xenobiotic metabolizing enzymes |
title_full | Inhibitory effect of purple rice husk extract on AFB(1)-induced micronucleus formation in rat liver through modulation of xenobiotic metabolizing enzymes |
title_fullStr | Inhibitory effect of purple rice husk extract on AFB(1)-induced micronucleus formation in rat liver through modulation of xenobiotic metabolizing enzymes |
title_full_unstemmed | Inhibitory effect of purple rice husk extract on AFB(1)-induced micronucleus formation in rat liver through modulation of xenobiotic metabolizing enzymes |
title_short | Inhibitory effect of purple rice husk extract on AFB(1)-induced micronucleus formation in rat liver through modulation of xenobiotic metabolizing enzymes |
title_sort | inhibitory effect of purple rice husk extract on afb(1)-induced micronucleus formation in rat liver through modulation of xenobiotic metabolizing enzymes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6724366/ https://www.ncbi.nlm.nih.gov/pubmed/31481128 http://dx.doi.org/10.1186/s12906-019-2647-9 |
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