Inhibitory Effect of Thai Purple Rice Husk Extract on Chemically Induced Carcinogenesis in Rats

This study investigated the cancer chemopreventive effects of an acidic methanol extract of purple rice husk on chemically induced carcinogenesis in rats. This purple rice husk extract (PRHE) had high polyphenol contents. Vanillic acid was a major phenolic compound in PRHE. Three major anthocyanins...

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Published in:Molecules
Main Authors: Charatda Punvittayagul, Arpamas Chariyakornkul, Paweena Sankam, Rawiwan Wongpoomchai
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Subjects:
Online Access:https://www.mdpi.com/1420-3049/26/2/360
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author Charatda Punvittayagul
Arpamas Chariyakornkul
Paweena Sankam
Rawiwan Wongpoomchai
author_facet Charatda Punvittayagul
Arpamas Chariyakornkul
Paweena Sankam
Rawiwan Wongpoomchai
author_sort Charatda Punvittayagul
collection DOAJ
container_title Molecules
description This study investigated the cancer chemopreventive effects of an acidic methanol extract of purple rice husk on chemically induced carcinogenesis in rats. This purple rice husk extract (PRHE) had high polyphenol contents. Vanillic acid was a major phenolic compound in PRHE. Three major anthocyanins found in PRHE were malvidin-3-glucoside, peonidin-3-glucoside and cyanidin-3-glucoside. PRHE was not toxic and clastogenic in rats. The LD<sub>50</sub> of PRHE was greater than 2000 mg kg<sup>−1</sup> body weight (BW). The oral administration of 300 or 1000 mg kg<sup>−1</sup> BW of PRHE for 28 days significantly decreased the number of micronucleated hepatocytes in diethylnitrosamine-initiated rats. The inhibitory mechanisms were associated with the reduction of cytochrome P450 2E1 expression and induction of some detoxifying enzymes in the liver. In addition, treatment with 500 mg kg<sup>−1</sup> BW of PRHE for eight weeks did not induce preneoplastic lesions in the liver and colon. It significantly inhibited hepatic glutathione-<i>S</i>-transferase positive foci formation induced by diethylnitrosamine and 1,2-dimethylhydrazine by suppression of hepatocyte proliferation and induction of apoptosis. In conclusion, PRHE did not present toxicity, clastogenicity or carcinogenicity in rats. It exhibited cancer chemopreventive properties against chemically induced early stages rat hepatocarcinogenesis. Anthocyanins and vanillic acid might be candidate anticarcinogenic compounds in purple rice husk.
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spelling doaj-art-9e48bb089f034dc9b938dc70aed0d4cd2025-08-19T23:00:19ZengMDPI AGMolecules1420-30492021-01-0126236010.3390/molecules26020360Inhibitory Effect of Thai Purple Rice Husk Extract on Chemically Induced Carcinogenesis in RatsCharatda Punvittayagul0Arpamas Chariyakornkul1Paweena Sankam2Rawiwan Wongpoomchai3Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, ThailandDepartment of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, ThailandSankamphaeng School, Saimun Sankamphaeng, San Kamphaeng, Chiang Mai 50130, ThailandDepartment of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, ThailandThis study investigated the cancer chemopreventive effects of an acidic methanol extract of purple rice husk on chemically induced carcinogenesis in rats. This purple rice husk extract (PRHE) had high polyphenol contents. Vanillic acid was a major phenolic compound in PRHE. Three major anthocyanins found in PRHE were malvidin-3-glucoside, peonidin-3-glucoside and cyanidin-3-glucoside. PRHE was not toxic and clastogenic in rats. The LD<sub>50</sub> of PRHE was greater than 2000 mg kg<sup>−1</sup> body weight (BW). The oral administration of 300 or 1000 mg kg<sup>−1</sup> BW of PRHE for 28 days significantly decreased the number of micronucleated hepatocytes in diethylnitrosamine-initiated rats. The inhibitory mechanisms were associated with the reduction of cytochrome P450 2E1 expression and induction of some detoxifying enzymes in the liver. In addition, treatment with 500 mg kg<sup>−1</sup> BW of PRHE for eight weeks did not induce preneoplastic lesions in the liver and colon. It significantly inhibited hepatic glutathione-<i>S</i>-transferase positive foci formation induced by diethylnitrosamine and 1,2-dimethylhydrazine by suppression of hepatocyte proliferation and induction of apoptosis. In conclusion, PRHE did not present toxicity, clastogenicity or carcinogenicity in rats. It exhibited cancer chemopreventive properties against chemically induced early stages rat hepatocarcinogenesis. Anthocyanins and vanillic acid might be candidate anticarcinogenic compounds in purple rice husk.https://www.mdpi.com/1420-3049/26/2/3601,2-dimethylhydrazineaberrant crypt focidiethylnitrosamineGST-P-positive focipurple rice husk
spellingShingle Charatda Punvittayagul
Arpamas Chariyakornkul
Paweena Sankam
Rawiwan Wongpoomchai
Inhibitory Effect of Thai Purple Rice Husk Extract on Chemically Induced Carcinogenesis in Rats
1,2-dimethylhydrazine
aberrant crypt foci
diethylnitrosamine
GST-P-positive foci
purple rice husk
title Inhibitory Effect of Thai Purple Rice Husk Extract on Chemically Induced Carcinogenesis in Rats
title_full Inhibitory Effect of Thai Purple Rice Husk Extract on Chemically Induced Carcinogenesis in Rats
title_fullStr Inhibitory Effect of Thai Purple Rice Husk Extract on Chemically Induced Carcinogenesis in Rats
title_full_unstemmed Inhibitory Effect of Thai Purple Rice Husk Extract on Chemically Induced Carcinogenesis in Rats
title_short Inhibitory Effect of Thai Purple Rice Husk Extract on Chemically Induced Carcinogenesis in Rats
title_sort inhibitory effect of thai purple rice husk extract on chemically induced carcinogenesis in rats
topic 1,2-dimethylhydrazine
aberrant crypt foci
diethylnitrosamine
GST-P-positive foci
purple rice husk
url https://www.mdpi.com/1420-3049/26/2/360
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AT arpamaschariyakornkul inhibitoryeffectofthaipurplericehuskextractonchemicallyinducedcarcinogenesisinrats
AT paweenasankam inhibitoryeffectofthaipurplericehuskextractonchemicallyinducedcarcinogenesisinrats
AT rawiwanwongpoomchai inhibitoryeffectofthaipurplericehuskextractonchemicallyinducedcarcinogenesisinrats