Role of ferulic acid in the amelioration of ionizing radiation induced inflammation: a murine model.

Ionizing radiation is responsible for oxidative stress by generating reactive oxygen species (ROS), which alters the cellular redox potential. This change activates several redox sensitive enzymes which are crucial in activating signaling pathways at molecular level and can lead to oxidative stress...

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Main Authors: Ujjal Das, Krishnendu Manna, Mahuya Sinha, Sanjukta Datta, Dipesh Kr Das, Anindita Chakraborty, Mahua Ghosh, Krishna Das Saha, Sanjit Dey
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4031149?pdf=render
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author Ujjal Das
Krishnendu Manna
Mahuya Sinha
Sanjukta Datta
Dipesh Kr Das
Anindita Chakraborty
Mahua Ghosh
Krishna Das Saha
Sanjit Dey
author_facet Ujjal Das
Krishnendu Manna
Mahuya Sinha
Sanjukta Datta
Dipesh Kr Das
Anindita Chakraborty
Mahua Ghosh
Krishna Das Saha
Sanjit Dey
author_sort Ujjal Das
collection DOAJ
description Ionizing radiation is responsible for oxidative stress by generating reactive oxygen species (ROS), which alters the cellular redox potential. This change activates several redox sensitive enzymes which are crucial in activating signaling pathways at molecular level and can lead to oxidative stress induced inflammation. Therefore, the present study was intended to assess the anti-inflammatory role of ferulic acid (FA), a plant flavonoid, against radiation-induced oxidative stress with a novel mechanistic viewpoint. FA was administered (50 mg/kg body wt) to Swiss albino mice for five consecutive days prior to exposing them to a single dose of 10 Gy 60Co γ-irradiation. The dose of FA was optimized from the survival experiment and 50 mg/kg body wt dose showed optimum effect. FA significantly ameliorated the radiation induced inflammatory response such as phosphorylation of IKKα/β and IκBα and consequent nuclear translocation of nuclear factor kappa B (NF-κB). FA also prevented the increase of cycloxygenase-2 (Cox-2) protein, inducible nitric oxide synthase-2 (iNOS-2) gene expression, lipid peroxidation in liver and the increase of tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6) in serum. It was observed that exposure to radiation results in decreased activity of superoxide dismutase (SOD), catalase (CAT) and the pool of reduced glutathione (GSH) content. However, FA treatment prior to irradiation increased the activities of the same endogenous antioxidants. Thus, pretreatment with FA offers protection against gamma radiation induced inflammation.
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spelling doaj.art-acd6b837b62a479980a1b360070936412022-12-22T03:38:19ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0195e9759910.1371/journal.pone.0097599Role of ferulic acid in the amelioration of ionizing radiation induced inflammation: a murine model.Ujjal DasKrishnendu MannaMahuya SinhaSanjukta DattaDipesh Kr DasAnindita ChakrabortyMahua GhoshKrishna Das SahaSanjit DeyIonizing radiation is responsible for oxidative stress by generating reactive oxygen species (ROS), which alters the cellular redox potential. This change activates several redox sensitive enzymes which are crucial in activating signaling pathways at molecular level and can lead to oxidative stress induced inflammation. Therefore, the present study was intended to assess the anti-inflammatory role of ferulic acid (FA), a plant flavonoid, against radiation-induced oxidative stress with a novel mechanistic viewpoint. FA was administered (50 mg/kg body wt) to Swiss albino mice for five consecutive days prior to exposing them to a single dose of 10 Gy 60Co γ-irradiation. The dose of FA was optimized from the survival experiment and 50 mg/kg body wt dose showed optimum effect. FA significantly ameliorated the radiation induced inflammatory response such as phosphorylation of IKKα/β and IκBα and consequent nuclear translocation of nuclear factor kappa B (NF-κB). FA also prevented the increase of cycloxygenase-2 (Cox-2) protein, inducible nitric oxide synthase-2 (iNOS-2) gene expression, lipid peroxidation in liver and the increase of tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6) in serum. It was observed that exposure to radiation results in decreased activity of superoxide dismutase (SOD), catalase (CAT) and the pool of reduced glutathione (GSH) content. However, FA treatment prior to irradiation increased the activities of the same endogenous antioxidants. Thus, pretreatment with FA offers protection against gamma radiation induced inflammation.http://europepmc.org/articles/PMC4031149?pdf=render
spellingShingle Ujjal Das
Krishnendu Manna
Mahuya Sinha
Sanjukta Datta
Dipesh Kr Das
Anindita Chakraborty
Mahua Ghosh
Krishna Das Saha
Sanjit Dey
Role of ferulic acid in the amelioration of ionizing radiation induced inflammation: a murine model.
PLoS ONE
title Role of ferulic acid in the amelioration of ionizing radiation induced inflammation: a murine model.
title_full Role of ferulic acid in the amelioration of ionizing radiation induced inflammation: a murine model.
title_fullStr Role of ferulic acid in the amelioration of ionizing radiation induced inflammation: a murine model.
title_full_unstemmed Role of ferulic acid in the amelioration of ionizing radiation induced inflammation: a murine model.
title_short Role of ferulic acid in the amelioration of ionizing radiation induced inflammation: a murine model.
title_sort role of ferulic acid in the amelioration of ionizing radiation induced inflammation a murine model
url http://europepmc.org/articles/PMC4031149?pdf=render
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