نمایش مختصر رکورد

dc.contributor.authorShokrgozar, Mohammad Alien_US
dc.contributor.authorHabibi Roudkenar, Mehryaren_US
dc.contributor.authorBahmani, Parisaen_US
dc.contributor.authorHalabian, Rahelehen_US
dc.contributor.authorMohammadi Roushandeh, Amanehen_US
dc.contributor.authorJahanian Najafabadi, Alien_US
dc.date.accessioned1399-07-30T20:54:30Zfa_IR
dc.date.accessioned2020-10-21T20:54:30Z
dc.date.available1399-07-30T20:54:30Zfa_IR
dc.date.available2020-10-21T20:54:30Z
dc.date.issued2012-03-01en_US
dc.date.issued1390-12-11fa_IR
dc.date.submitted2013-11-30en_US
dc.date.submitted1392-09-09fa_IR
dc.identifier.citationShokrgozar, Mohammad Ali, Habibi Roudkenar, Mehryar, Bahmani, Parisa, Halabian, Raheleh, Mohammadi Roushandeh, Amaneh, Jahanian Najafabadi, Ali. (2012). HESA-A Exerts Its Cytoprotective Effects through Scavenging of Free Radicals: An in Vitro Study. Iranian Journal of Medical Sciences, 37(1), 47-53.en_US
dc.identifier.issn0253-0716
dc.identifier.issn1735-3688
dc.identifier.urihttps://ijms.sums.ac.ir/article_39536.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/439164
dc.description.abstractBackground: Natural medicines have been recently considered more reasonable for human use most notably due to their safety and tolerance. HESA-A is a marine-originated herbal medicine with a variety of healing effects. However, its exact biological mechanism is not clear. The pre-sent study aimed at the evaluation of the HESA-A antioxidant effect.<br /> Methods: Chinese hamster ovary (CHO) and human embryonic kidney (HEK293T) cells were treated with different concentrations of HESA-A and H2O2 followed by cell proliferation assays. The antioxidant effect of the HESA-A preparations was evaluated by an antioxidant assay kit.<br /> Results: The viability of CHO and HEK293T cells were about 89% following their incubation with 100 and 200 ng/ml HESA-A, respectively for 1.5 hrs. However, when the cells were incubated with concentrations of 300 ng/ml or more, the cell viability significantly decreased to 48% compare to the control cells. The cytotoxic effects of H2O2 were observed after 2 hrs of incubation of the HEK293T or CHO cells with 10 mM or 16 mM H2O2, respectively, while in the presence of HESA-A the cytotoxicity was significantly decreased. Antioxidant assay revealed that HESA-A scavenges free radicals.<br /> Conclusion: The findings indicate that HESA-A had cytoprotective effects in vitro, and that such an effect might be due to antioxidant properties.en_US
dc.languageEnglish
dc.language.isoen_US
dc.publisherShiraz University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Medical Sciencesen_US
dc.subjectHESA-Aen_US
dc.subjectReactive Oxygen Speciesen_US
dc.subjectHydrogen peroxideen_US
dc.titleHESA-A Exerts Its Cytoprotective Effects through Scavenging of Free Radicals: An in Vitro Studyen_US
dc.typeTexten_US
dc.typeOriginal Article(s)en_US
dc.contributor.departmentNational Cell Bank of Iran, Pasteur Institute of Iran, Tehran, Iranen_US
dc.contributor.departmentBlood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iranen_US
dc.contributor.departmentBlood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iranen_US
dc.contributor.departmentBlood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iranen_US
dc.contributor.departmentDepartment of Anatomy, Faculty of Medicine, Medical University of Hamadan, Hamadan, Iranen_US
dc.contributor.departmentDepartment of Molecular Biology, Pasteur Institute of Iran, Tehran, Iranen_US
dc.citation.volume37
dc.citation.issue1
dc.citation.spage47
dc.citation.epage53


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