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dc.contributor.authorRefahi, S
dc.contributor.authorPourissa, M
dc.contributor.authorZirak, MR
dc.contributor.authorHadadi, G
dc.date.accessioned2018-08-26T07:43:25Z
dc.date.available2018-08-26T07:43:25Z
dc.date.issued2015
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/47998
dc.description.abstractTo evaluate the ability of glycyrrhizic acid (GLA) to reduce the tumor necrosis factor (TNF-), release on messenger ribonucleic acid (mRNA) and protein production in the lungs using GLA in response to irradiation were studied. The animals were divided into four groups: No treatment (NT group), GLA treatment only (GLA group), irradiation only (XRT group), and GLA treatment plus irradiation (GLA/XRT group). Rats were killed at different time points. Real-time reverse transcriptase polymerase chain reaction (RT-PCR) was used to evaluate the mRNA expression of TNF- in the lungs (compared with non-irradiated lungs). An enzyme-linked immunosorbant assay (ELISA) assay was used to measure the TNF- protein level. The TNF- mRNA expression in the lungs of the XRT rats was clearly higher at all-time points compared to the NT rats. The TNF- mRNA expression in the lungs of the GLA/XRT rats was lower at all-time points compared to the XRT rats. Release of the TNF- on protein level in the lungs of the XRT rats increased at all-time points compared to the NT rats. In contrast to the XRT rats, the lungs of the GLA/XRT rats revealed a reduction on TNF- protein level at 6 h after irradiation. This study has clearly showed the immediate down-regulation of the TNF- mRNA and protein production in the lungs using GLA in response to irradiation.
dc.language.isoEnglish
dc.relation.ispartofJOURNAL OF MEDICAL PHYSICS
dc.subjectGlycyrrhizic acid
dc.subjectradiation-induced lung damage
dc.subjecttumor necrosis factor
dc.titleModulation expression of tumor necrosis factor alpha in the radiation-induced lung injury by glycyrrhizic acid
dc.typeArticle
dc.citation.volume40
dc.citation.issue2
dc.citation.spage95
dc.citation.epage101
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.4103/0971-6203.158689


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