Pyrrolidinedithiocarbamate attenuates bleomycin-induced pulmonary fibrosis in rats: Modulation of oxidative stress, fibrosis, and inflammatory parameters

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorZaafan M.A.
dc.contributor.authorZaki H.F.
dc.contributor.authorEl-Brairy A.I.
dc.contributor.authorKenawy S.A.
dc.contributor.otherOctober University for Modern Sciences and Arts MSA
dc.date.accessioned2020-01-09T20:41:30Z
dc.date.available2020-01-09T20:41:30Z
dc.date.issued31-10-2016
dc.descriptionSJR 2025 0.553 Q2 H-Index 60 Subject Area and Category: Biochemistry, Genetics and Molecular Biology Clinical Biochemistry Molecular Biology Medicine Pulmonary and Respiratory Medicine
dc.description.abstractObjective: The current study aimed to investigate the modulatory effects of pyrrolidinedithiocarbamate (PDTC; 100 mg/kg) on bleomycin-induced pulmonary fibrosis (5 mg/kg; intratracheal) in rats. Materials and methods: Rats were randomly assigned to three groups: normal control, bleomycin control, and PDTC-treated groups. Lung injury was evaluated through histological examination, immunohistochemical detection of inducible nitric oxide synthase (iNOS) in lung tissue and evaluating the total and differential leucocytes count in bronchoalveolar lavage fluid. Lung tissue was used for biochemical assessment of lung content of hydroxyproline, transforming growth factor beta-1 (TGF-β1), tumor necrosis factor-alpha (TNF-α) as well as analysis of lipid peroxides, reduced glutathione (GSH), and total nitrite contents. Results: PDTC attenuated bleomycin-induced pulmonary fibrosis as evidenced by histological observations, decreased iNOS expression and prevention of bleomycin-induced altered total and differential leukocytes count. Additionally, PDTC caused a significant decrease in lung contents of hydroxyproline, TGF-β1, TNF-α, lipid peroxides, and total nitrite coupled with increase in lung GSH content as compared to bleomycin control group. Conclusion: PDTC attenuated bleomycin-induced pulmonary fibrosis in rats via its anti-inflammatory, antioxidant, and antifibrotic activities.en_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=18480&tip=sid&clean=0
dc.identifier.citationZaafan, M. A., Zaki, H. F., El-Brairy, A. I., & Kenawy, S. A. (2016). Pyrrolidinedithiocarbamate attenuates bleomycin-induced pulmonary fibrosis in rats: Modulation of oxidative stress, fibrosis, and inflammatory parameters. Experimental Lung Research, 42(8-10), 408–416. https://doi.org/10.1080/01902148.2016.1244578 ‌
dc.identifier.doihttps://doi.org/10.1080/01902148.2016.1244578
dc.identifier.issn1902148
dc.identifier.otherhttps://doi.org/10.1080/01902148.2016.1244578
dc.identifier.urihttps://t.ly/BXOqX
dc.language.isoEnglishen_US
dc.publisherTaylor and Francis Ltden_US
dc.relation.ispartofseriesExperimental Lung Research ; Volume 42, 2016 , Issue 8-10
dc.subjectbleomycin; nitric oxide; pulmonary fibrosis; pyrrolidinedithiocarbamate; tumor necrosis factor-alpha.en_US
dc.titlePyrrolidinedithiocarbamate attenuates bleomycin-induced pulmonary fibrosis in rats: Modulation of oxidative stress, fibrosis, and inflammatory parametersen_US
dc.typeArticleen_US
dcterms.sourceScopus

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