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Anti-Inflammatory Property of Plantago major Leaf Extract Reduces the Inflammatory Reaction in Experimental Acetaminophen-Induced Liver Injury

Hepatic injury induces inflammatory process and cell necrosis. Plantago major is traditionally used for various diseases. This study aimed to determine the anti-inflammatory property of P. major leaf extracts on inflammatory reaction following acetaminophen (APAP) hepatotoxicity. Thirty male Sprague...

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Autores principales: Hussan, Farida, Mansor, Adila Sofea, Hassan, Siti Nazihahasma, Tengku Nor Effendy Kamaruddin, Tg. Nurul Tasnim, Budin, Siti Balkis, Othman, Faizah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537734/
https://www.ncbi.nlm.nih.gov/pubmed/26300946
http://dx.doi.org/10.1155/2015/347861
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author Hussan, Farida
Mansor, Adila Sofea
Hassan, Siti Nazihahasma
Tengku Nor Effendy Kamaruddin, Tg. Nurul Tasnim
Budin, Siti Balkis
Othman, Faizah
author_facet Hussan, Farida
Mansor, Adila Sofea
Hassan, Siti Nazihahasma
Tengku Nor Effendy Kamaruddin, Tg. Nurul Tasnim
Budin, Siti Balkis
Othman, Faizah
author_sort Hussan, Farida
collection PubMed
description Hepatic injury induces inflammatory process and cell necrosis. Plantago major is traditionally used for various diseases. This study aimed to determine the anti-inflammatory property of P. major leaf extracts on inflammatory reaction following acetaminophen (APAP) hepatotoxicity. Thirty male Sprague-Dawley rats were divided into 5 groups, namely, normal control (C), APAP, aqueous (APAP + AQ), methanol (APAP + MT), and ethanol (APAP + ET) extract treated groups. All APAP groups received oral APAP (2 g/kg) at day 0. Then, 1000 mg/kg dose of P. major extracts was given for six days. The levels of liver transaminases were measured at day 1 and day 7 after APAP induction. At day 7, the blood and liver tissue were collected to determine plasma cytokines and tissue 11β-HSD type 1 enzyme. The in vitro anti-inflammatory activities of methanol, ethanol, and aqueous extracts were 26.74 ± 1.6%, 21.69 ± 2.81%, and 12.23 ± 3.15%, respectively. The ALT and AST levels were significantly higher in the APAP groups at day 1 whereas the enzyme levels of all groups showed no significant difference at day 7. The extracts treatment significantly reduced the proinflammatory cytokine levels and significantly increased the 11β-HSD type 1 enzyme activity (p < 0.05). In conclusion, the P. major extracts attenuate the inflammatory reaction following APAP-induced liver injury.
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spelling pubmed-45377342015-08-23 Anti-Inflammatory Property of Plantago major Leaf Extract Reduces the Inflammatory Reaction in Experimental Acetaminophen-Induced Liver Injury Hussan, Farida Mansor, Adila Sofea Hassan, Siti Nazihahasma Tengku Nor Effendy Kamaruddin, Tg. Nurul Tasnim Budin, Siti Balkis Othman, Faizah Evid Based Complement Alternat Med Research Article Hepatic injury induces inflammatory process and cell necrosis. Plantago major is traditionally used for various diseases. This study aimed to determine the anti-inflammatory property of P. major leaf extracts on inflammatory reaction following acetaminophen (APAP) hepatotoxicity. Thirty male Sprague-Dawley rats were divided into 5 groups, namely, normal control (C), APAP, aqueous (APAP + AQ), methanol (APAP + MT), and ethanol (APAP + ET) extract treated groups. All APAP groups received oral APAP (2 g/kg) at day 0. Then, 1000 mg/kg dose of P. major extracts was given for six days. The levels of liver transaminases were measured at day 1 and day 7 after APAP induction. At day 7, the blood and liver tissue were collected to determine plasma cytokines and tissue 11β-HSD type 1 enzyme. The in vitro anti-inflammatory activities of methanol, ethanol, and aqueous extracts were 26.74 ± 1.6%, 21.69 ± 2.81%, and 12.23 ± 3.15%, respectively. The ALT and AST levels were significantly higher in the APAP groups at day 1 whereas the enzyme levels of all groups showed no significant difference at day 7. The extracts treatment significantly reduced the proinflammatory cytokine levels and significantly increased the 11β-HSD type 1 enzyme activity (p < 0.05). In conclusion, the P. major extracts attenuate the inflammatory reaction following APAP-induced liver injury. Hindawi Publishing Corporation 2015 2015-08-02 /pmc/articles/PMC4537734/ /pubmed/26300946 http://dx.doi.org/10.1155/2015/347861 Text en Copyright © 2015 Farida Hussan et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hussan, Farida
Mansor, Adila Sofea
Hassan, Siti Nazihahasma
Tengku Nor Effendy Kamaruddin, Tg. Nurul Tasnim
Budin, Siti Balkis
Othman, Faizah
Anti-Inflammatory Property of Plantago major Leaf Extract Reduces the Inflammatory Reaction in Experimental Acetaminophen-Induced Liver Injury
title Anti-Inflammatory Property of Plantago major Leaf Extract Reduces the Inflammatory Reaction in Experimental Acetaminophen-Induced Liver Injury
title_full Anti-Inflammatory Property of Plantago major Leaf Extract Reduces the Inflammatory Reaction in Experimental Acetaminophen-Induced Liver Injury
title_fullStr Anti-Inflammatory Property of Plantago major Leaf Extract Reduces the Inflammatory Reaction in Experimental Acetaminophen-Induced Liver Injury
title_full_unstemmed Anti-Inflammatory Property of Plantago major Leaf Extract Reduces the Inflammatory Reaction in Experimental Acetaminophen-Induced Liver Injury
title_short Anti-Inflammatory Property of Plantago major Leaf Extract Reduces the Inflammatory Reaction in Experimental Acetaminophen-Induced Liver Injury
title_sort anti-inflammatory property of plantago major leaf extract reduces the inflammatory reaction in experimental acetaminophen-induced liver injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537734/
https://www.ncbi.nlm.nih.gov/pubmed/26300946
http://dx.doi.org/10.1155/2015/347861
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