Effects of thymoquinone on alpha-amanitin induced hepatotoxicity in human C3A hepatocytes
dc.authorid | kaya, ertugrul/0000-0003-0081-682X | |
dc.authorid | Yılmaz, İsmail/0000-0002-4474-9617 | |
dc.authorwosid | kaya, ertugrul/C-1505-2013 | |
dc.contributor.author | Katırcı, Yavuz | |
dc.contributor.author | Yılmaz, İsmail | |
dc.contributor.author | Kaya, Ertuğrul | |
dc.date.accessioned | 2023-07-26T11:57:19Z | |
dc.date.available | 2023-07-26T11:57:19Z | |
dc.date.issued | 2022 | |
dc.department | DÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Tıbbi Farmakoloji Ana Bilim Dalı | en_US |
dc.description.abstract | Thymoquinone (TQ) has shown hepatoprotective effects in various experimental studies. We aimed to investigate the possible beneficial effects of TQ regarding its prevention of alpha-amanitin induced hepatotoxicity in human C3A hepatocytes. After administering alpha-amanitin in a concentrations of 1 and 10 mu g/mL on the cells in a hepatocyte cell line, TQ was administered in various concentrations (10, 5, 1, 0.5, 0.1, 0.05, 0.01, 0.005 mu g/mL). The MTT test was used to determine cell viability. For the groups given only TQ at various concentrations, the cell viability rates at 48 hours post-administration were found at 82.6, 98.3, 102.1, 102.5, 99.4, 99.4, 101.9 and 106.3%, respectively. For the group with 1 mu g/mL alpha-amanitin and various TQ concentrations, the cell viability rates were found at 74.6, 88.5, 87.4, 88.7, 85.7, 86.8, 88.4, and 92.9%, respectively. For the group with 10 mu g/mL alpha-amanitin and various TQ concentrations, the cell viability rates for each TQ subgroup were found at 65.2, 79.2, 81.4, 81.1, 81.8, 81.8, 82.2 and 91.9%, respectively. Our study is the first in vitro study that investigates TQ's effects on alpha-amanitin induced hepatotoxicity. Although TQ had beneficial effect in low doses did not significantly increase cell viability in liver damage due to alpha-amanitin toxicity. | en_US |
dc.identifier.doi | 10.1590/s2175-97902022e191072 | |
dc.identifier.issn | 1984-8250 | |
dc.identifier.issn | 2175-9790 | |
dc.identifier.scopus | 2-s2.0-85134557982 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.uri | https://doi.org/10.1590/s2175-97902022e191072 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12684/13123 | |
dc.identifier.volume | 58 | en_US |
dc.identifier.wos | WOS:000836190400001 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.institutionauthor | Kaya, Ertuğrul | |
dc.language.iso | en | en_US |
dc.publisher | Univ Sao Paulo, Conjunto Quimicas | en_US |
dc.relation.ispartof | Brazilian Journal of Pharmaceutical Sciences | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.snmz | $2023V1Guncelleme$ | en_US |
dc.subject | Thymoquinone; Alpha-Amanitin; Hepatotoxicity; Mtt Assay; C3a Human Hepatocyte Cell Line | en_US |
dc.subject | Nigella-Sativa; Oxidative Stress; N-Acetylcysteine; Urtica-Dioica; Toxicity; Mice; Purification; Constituent; Generation; Phalloides | en_US |
dc.title | Effects of thymoquinone on alpha-amanitin induced hepatotoxicity in human C3A hepatocytes | en_US |
dc.type | Article | en_US |
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