| dc.contributor.author | Shokrgozar, Mohammad Ali | en_US |
| dc.contributor.author | Habibi Roudkenar, Mehryar | en_US |
| dc.contributor.author | Bahmani, Parisa | en_US |
| dc.contributor.author | Halabian, Raheleh | en_US |
| dc.contributor.author | Mohammadi Roushandeh, Amaneh | en_US |
| dc.contributor.author | Jahanian Najafabadi, Ali | en_US |
| dc.date.accessioned | 1399-07-30T20:54:30Z | fa_IR |
| dc.date.accessioned | 2020-10-21T20:54:30Z | |
| dc.date.available | 1399-07-30T20:54:30Z | fa_IR |
| dc.date.available | 2020-10-21T20:54:30Z | |
| dc.date.issued | 2012-03-01 | en_US |
| dc.date.issued | 1390-12-11 | fa_IR |
| dc.date.submitted | 2013-11-30 | en_US |
| dc.date.submitted | 1392-09-09 | fa_IR |
| dc.identifier.citation | Shokrgozar, 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.issn | 0253-0716 | |
| dc.identifier.issn | 1735-3688 | |
| dc.identifier.uri | https://ijms.sums.ac.ir/article_39536.html | |
| dc.identifier.uri | https://iranjournals.nlai.ir/handle/123456789/439164 | |
| dc.description.abstract | Background: 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.language | English | |
| dc.language.iso | en_US | |
| dc.publisher | Shiraz University of Medical Sciences | en_US |
| dc.relation.ispartof | Iranian Journal of Medical Sciences | en_US |
| dc.subject | HESA-A | en_US |
| dc.subject | Reactive Oxygen Species | en_US |
| dc.subject | Hydrogen peroxide | en_US |
| dc.title | HESA-A Exerts Its Cytoprotective Effects through Scavenging of Free Radicals: An in Vitro Study | en_US |
| dc.type | Text | en_US |
| dc.type | Original Article(s) | en_US |
| dc.contributor.department | National Cell Bank of Iran, Pasteur Institute of Iran, Tehran, Iran | en_US |
| dc.contributor.department | Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran | en_US |
| dc.contributor.department | Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran | en_US |
| dc.contributor.department | Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran | en_US |
| dc.contributor.department | Department of Anatomy, Faculty of Medicine, Medical University of Hamadan, Hamadan, Iran | en_US |
| dc.contributor.department | Department of Molecular Biology, Pasteur Institute of Iran, Tehran, Iran | en_US |
| dc.citation.volume | 37 | |
| dc.citation.issue | 1 | |
| dc.citation.spage | 47 | |
| dc.citation.epage | 53 | |