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Effects of taxifolin on tramadol-induced oxidative and inflammatory liver injury in rats: an experimental study

紫杉醇 氧化应激 丙二醛 医学 内科学 炎症 谷胱甘肽 肝损伤 内分泌学 抗氧化剂 病理 化学 生物化学 类黄酮
作者
Tülay Ceren Ölmeztürk Karakurt,Nurhan Eren,Faruk Subaşı,Ufuk Kuyrukluyıldız,Taha Abdulkadir Çoban,Halis Süleyman,Behzad Mokhtare
出处
期刊:Drug and Chemical Toxicology [Taylor & Francis]
卷期号:47 (4): 457-462 被引量:4
标识
DOI:10.1080/01480545.2023.2199175
摘要

In this experimental study we aimed to investigate the biochemical and histopathological effects of concomitantly administered taxifolin on tramadol-induced liver damage in rats. The rats were divided into three groups; control group (CG), tramadol alone (TRG), and taxifolin + tramadol given (TTRG) groups. Malondialdehyde (MDA), total glutathione (tGSH), total oxidant status (TOS), total antioxidant status (TAS), nuclear factor-kappa beta (NF-kB), tumor necrosis factor-α (TNF-α), and interleukin-1β (IL-1β) levels were measured in liver tissues. Liver tissues were also examined histopathologically. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities were determined in blood samples. In tissue analyses, determinants of oxidative stress and inflammation, all were significantly higher in the TRG group compared with the control and TTRG groups. In the TTRG group, all oxidative stress and inflammation markers were significantly lower than in the TRG group. In addition, there was not any significant difference between the control and TTRG groups regarding the TOS and TAS status. Serum liver enzymes were also significantly higher in the TRG group than in the other two groups. In histopathological examinations, the control group had a normal histological appearance. Degenerative-necrotic hepatocytes and hemorrhage, which were seen at a severe level in the TRG group, were found to be moderate in the treated TTRG group. In addition, mononuclear cell infiltrations were found to be severe in the TRG group and mild in the treated TTRG group. Finally it was concluded that Taxifolin alleviated the toxic effects of tramadol on the liver including the histopathological and biochemical changes as well as the oxidative damage.
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