Department of Pharmacology, Faculty of Medicine, Minia University, Minia, Egypt.
Department of Histology and Cell Biology, Faculty of Medicine, Minia University, Minia, Egypt; Department of Histology and Cell Biology, Misr University for Science and Technology, Egypt.
Biomed Pharmacother. 2021 Feb;134:111063. doi: 10.1016/j.biopha.2020.111063. Epub 2020 Dec 24.
Liver ischemia-reperfusion (I/R) injury is an inescapable problem. Diacerein, a chondro-protective drug, has antioxidant and anti-inflammatory effects. Its effect on liver I/R injury has not yet been fully clarified. Therefore, the current study aimed to detect its hepatic protective effect with the explanation of possible underlying mechanisms.
Adult male albino rats were assigned to 4 groups: sham group, diacerein pretreated sham group, I/R non-treated group, and I/R diacerein pretreated group. Serum liver enzymes, hepatic tissue oxidative stress parameters, inflammatory biomarkers mainly Toll-like receptors-4 (TLR4), and liver fatty acid binding protein (L-FABP) levels were determined. Histopathological examination of liver tissues and immunohistochemical studies of heat shock protein 70, nuclear factor-kappa B, and Cluster of Differentiation 68 were also done.
Diacerein pretreatment has the ability to restore the hepatic I/R damaging effect, proved by the reduction of serum liver enzymes, the decrease of the oxidative stress and hepatic inflammation via down-regulation of TLR4/ NFκ-B signaling pathway together with the restoration of L-FABP level and improvement of the histopathological and immunohistochemical study findings in the hepatic tissue.
These results suggested the hepatoprotective effect of diacerein relies on its antioxidant and anti-inflammatory effects reducing TLR4/ NFκ-B signaling pathway.
肝脏缺血再灌注(I/R)损伤是一个不可避免的问题。二乙酰氨己酸是一种软骨保护药物,具有抗氧化和抗炎作用。其对肝脏 I/R 损伤的作用尚未完全阐明。因此,本研究旨在通过探讨其可能的作用机制,检测其肝保护作用。
将成年雄性白化大鼠分为 4 组:假手术组、二乙酰氨己酸预处理假手术组、未治疗 I/R 组和 I/R 二乙酰氨己酸预处理组。检测血清肝酶、肝组织氧化应激参数、主要的 Toll 样受体 4(TLR4)和肝型脂肪酸结合蛋白(L-FABP)水平等炎症生物标志物。还对肝组织进行了组织病理学检查和热休克蛋白 70、核因子-κB 和分化群 68 的免疫组化研究。
二乙酰氨己酸预处理具有恢复肝 I/R 损伤的能力,这一点通过降低血清肝酶、通过下调 TLR4/NFκB 信号通路降低氧化应激和肝炎症来证明,同时还恢复了 L-FABP 水平,并改善了肝组织的组织病理学和免疫组化研究结果。
这些结果表明,二乙酰氨己酸的肝保护作用依赖于其抗氧化和抗炎作用,降低 TLR4/NFκB 信号通路。