Polygonum minus essential oil modulates cisplatin-induced hepatotoxicity through inflammatory and apoptotic pathways

Oxidative stress, inflammation and apoptosis are thought as primary mediators of cisplatin-induced hepatotoxicity. The objective of this study was to determine the protective effect of Polygonum minus essential oil in cisplatin-induced hepatotoxicity. A total of forty-two male rats were randomly div...

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Published in:EXCLI Journal
Main Author: Rashid N.A.; Hussan F.; Hamid A.; Ridzuan N.R.A.; Halim S.A.S.A.; Jalil N.A.A.; Najib N.H.M.; Teoh S.L.; Budin S.B.
Format: Article
Language:English
Published: Leibniz Research Centre for Working Environment and Human Factors 2020
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85090677901&doi=10.17179%2fexcli2020-2355&partnerID=40&md5=13e4105d9ba212f27e35aa86bebddf82
id 2-s2.0-85090677901
spelling 2-s2.0-85090677901
Rashid N.A.; Hussan F.; Hamid A.; Ridzuan N.R.A.; Halim S.A.S.A.; Jalil N.A.A.; Najib N.H.M.; Teoh S.L.; Budin S.B.
Polygonum minus essential oil modulates cisplatin-induced hepatotoxicity through inflammatory and apoptotic pathways
2020
EXCLI Journal
19

10.17179/excli2020-2355
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85090677901&doi=10.17179%2fexcli2020-2355&partnerID=40&md5=13e4105d9ba212f27e35aa86bebddf82
Oxidative stress, inflammation and apoptosis are thought as primary mediators of cisplatin-induced hepatotoxicity. The objective of this study was to determine the protective effect of Polygonum minus essential oil in cisplatin-induced hepatotoxicity. A total of forty-two male rats were randomly divided into seven groups: control, cisplatin, β-caryophyllene 150 mg/kg (BCP), PmEO 100 mg/kg + cisplatin (PmEO100CP), PmEO 200 mg/kg + cisplatin (PmEO200CP), PmEO 400 mg/kg + cisplatin (PmEO400CP) and PmEO 400 mg/kg (PmEO400). Rats in the BCP, PmEO100CP, PmEO200CP, PmEO400CP and PmEO400 group received respective treatment orally for 14 con-secutive days prior to cisplatin injection. All animals except for those in the control group and PmEO400 were administered with a single dose of cisplatin (10 mg/kg) intraperitoneally on day 15 and all animals were sacrificed on day 18. PmEO100CP pretreatment protected against cisplatin-induced hepatotoxicity by decreasing CYP2E1 and indicators of oxidative stress including malondialdehyde, 8-OHdG and protein carbonyl which was accompa-nied by increased antioxidant status (glutathione, glutathione peroxidase, superoxide dismutase and catalase) as compared to cisplatin group. PmEO100CP pretreatment also modulated changes in liver inflammatory markers (TNF-α, IL-1α, IL-1β, IL-6 and IL-10). PmEO100CP administration also notably reduced cisplatin-induced apop-tosis significantly as compared to cisplatin group. In conclusion, our results suggested that P. minus essential oil at a dose of 100 mg/kg may protect against cisplatin-induced hepatotoxicity possibly via inhibition of oxidative stress, inflammation and apoptosis. © 2020, Leibniz Research Centre for Working Environment and Human Factors. All rights reserved.
Leibniz Research Centre for Working Environment and Human Factors
16112156
English
Article

author Rashid N.A.; Hussan F.; Hamid A.; Ridzuan N.R.A.; Halim S.A.S.A.; Jalil N.A.A.; Najib N.H.M.; Teoh S.L.; Budin S.B.
spellingShingle Rashid N.A.; Hussan F.; Hamid A.; Ridzuan N.R.A.; Halim S.A.S.A.; Jalil N.A.A.; Najib N.H.M.; Teoh S.L.; Budin S.B.
Polygonum minus essential oil modulates cisplatin-induced hepatotoxicity through inflammatory and apoptotic pathways
author_facet Rashid N.A.; Hussan F.; Hamid A.; Ridzuan N.R.A.; Halim S.A.S.A.; Jalil N.A.A.; Najib N.H.M.; Teoh S.L.; Budin S.B.
author_sort Rashid N.A.; Hussan F.; Hamid A.; Ridzuan N.R.A.; Halim S.A.S.A.; Jalil N.A.A.; Najib N.H.M.; Teoh S.L.; Budin S.B.
title Polygonum minus essential oil modulates cisplatin-induced hepatotoxicity through inflammatory and apoptotic pathways
title_short Polygonum minus essential oil modulates cisplatin-induced hepatotoxicity through inflammatory and apoptotic pathways
title_full Polygonum minus essential oil modulates cisplatin-induced hepatotoxicity through inflammatory and apoptotic pathways
title_fullStr Polygonum minus essential oil modulates cisplatin-induced hepatotoxicity through inflammatory and apoptotic pathways
title_full_unstemmed Polygonum minus essential oil modulates cisplatin-induced hepatotoxicity through inflammatory and apoptotic pathways
title_sort Polygonum minus essential oil modulates cisplatin-induced hepatotoxicity through inflammatory and apoptotic pathways
publishDate 2020
container_title EXCLI Journal
container_volume 19
container_issue
doi_str_mv 10.17179/excli2020-2355
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85090677901&doi=10.17179%2fexcli2020-2355&partnerID=40&md5=13e4105d9ba212f27e35aa86bebddf82
description Oxidative stress, inflammation and apoptosis are thought as primary mediators of cisplatin-induced hepatotoxicity. The objective of this study was to determine the protective effect of Polygonum minus essential oil in cisplatin-induced hepatotoxicity. A total of forty-two male rats were randomly divided into seven groups: control, cisplatin, β-caryophyllene 150 mg/kg (BCP), PmEO 100 mg/kg + cisplatin (PmEO100CP), PmEO 200 mg/kg + cisplatin (PmEO200CP), PmEO 400 mg/kg + cisplatin (PmEO400CP) and PmEO 400 mg/kg (PmEO400). Rats in the BCP, PmEO100CP, PmEO200CP, PmEO400CP and PmEO400 group received respective treatment orally for 14 con-secutive days prior to cisplatin injection. All animals except for those in the control group and PmEO400 were administered with a single dose of cisplatin (10 mg/kg) intraperitoneally on day 15 and all animals were sacrificed on day 18. PmEO100CP pretreatment protected against cisplatin-induced hepatotoxicity by decreasing CYP2E1 and indicators of oxidative stress including malondialdehyde, 8-OHdG and protein carbonyl which was accompa-nied by increased antioxidant status (glutathione, glutathione peroxidase, superoxide dismutase and catalase) as compared to cisplatin group. PmEO100CP pretreatment also modulated changes in liver inflammatory markers (TNF-α, IL-1α, IL-1β, IL-6 and IL-10). PmEO100CP administration also notably reduced cisplatin-induced apop-tosis significantly as compared to cisplatin group. In conclusion, our results suggested that P. minus essential oil at a dose of 100 mg/kg may protect against cisplatin-induced hepatotoxicity possibly via inhibition of oxidative stress, inflammation and apoptosis. © 2020, Leibniz Research Centre for Working Environment and Human Factors. All rights reserved.
publisher Leibniz Research Centre for Working Environment and Human Factors
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