Laboratory of Human Genome and Multifactorial Diseases (LR12ES07), Faculty of Pharmacy, University of Monastir, Avicenne Street, 5019, Monastir, Tunisia.
Laboratory of Histology, Embryology and Cytogenetics (LR18ES40), Faculty of Medicine, University of Monastir, Avicenne Street, 5019, Monastir, Tunisia.
Inflammation. 2023 Aug;46(4):1221-1235. doi: 10.1007/s10753-023-01802-9. Epub 2023 Mar 18.
Ischemia/reperfusion injury (IRI) is an inevitable complication of liver surgery and transplantation. The purpose of this study was to examine the beneficial effects of diclofenac on hepatic IRI and the mechanism behind it. Wistar rats' livers were subjected to warm ischemia for 60 min followed by 24 h of reperfusion. Diclofenac was administered intravenously 15 min before ischemia at 10, 20, and 40 mg/kg body weight. To determine the mechanism of diclofenac protection, the NOS inhibitor L-Nitro-arginine methyl ester (L-NAME) was administered intravenously 10 min after diclofenac injection (40 mg/kg). Liver injury was evaluated by aminotransferases (ALT and AST) activities and histopathological analysis. Oxidative stress parameters (SOD, GPX, MPO, GSH, MDA, and PSH) were also determined. Then, eNOS gene transcription and p-eNOS and iNOS protein expressions were evaluated. The transcription factors PPAR-γ and NF-κB in addition to the regulatory protein IκBα were also investigated. Finally, the gene expression levels of inflammatory (COX-2, IL-6, IL-1β, IL-18, TNF-α, HMGB-1, and TLR-4) and apoptosis (Bcl-2 and Bax) markers were measured. Diclofenac, at the optimal dose of 40 mg/kg, decreased liver injury and maintained histological integrity. It also reduced oxidative stress, inflammation, and apoptosis. Its mechanism of action essentially depended on eNOS activation rather than COX-2 inhibition, since pre-treatment with L-NAME abolished all the protective effects of diclofenac. To our knowledge, this is the first study demonstrating that diclofenac protects rat liver against warm IRI through the induction of NO-dependent pathway. Diclofenac reduced oxidative balance, attenuated the activation of the subsequent pro-inflammatory response and decreased cellular and tissue damage. Therefore, diclofenac could be a promising molecule for the prevention of liver IRI.
缺血再灌注损伤(IRI)是肝外科和肝移植不可避免的并发症。本研究旨在探讨双氯芬酸对肝IRI的有益作用及其机制。Wistar 大鼠肝脏在缺血 60 分钟后进行热缺血,然后再进行 24 小时的再灌注。双氯芬酸在缺血前 15 分钟以 10、20 和 40mg/kg 体重静脉注射。为了确定双氯芬酸保护的机制,在双氯芬酸注射后 10 分钟静脉注射一氧化氮合酶抑制剂 L-Nitro-arginine methyl ester(L-NAME)(40mg/kg)。通过氨基转移酶(ALT 和 AST)活性和组织病理学分析评估肝损伤。还测定了氧化应激参数(SOD、GPX、MPO、GSH、MDA 和 PSH)。然后,评估 eNOS 基因转录和 p-eNOS 和 iNOS 蛋白表达。还研究了转录因子 PPAR-γ 和 NF-κB 以及调节蛋白 IκBα。最后,还测量了炎症(COX-2、IL-6、IL-1β、IL-18、TNF-α、HMGB-1 和 TLR-4)和凋亡(Bcl-2 和 Bax)标志物的基因表达水平。在最佳剂量 40mg/kg 时,双氯芬酸降低了肝损伤并维持了组织学完整性。它还降低了氧化应激、炎症和细胞凋亡。其作用机制主要依赖于 eNOS 激活而不是 COX-2 抑制,因为 L-NAME 的预处理消除了双氯芬酸的所有保护作用。据我们所知,这是第一项表明双氯芬酸通过诱导 NO 依赖途径保护大鼠肝脏免受热 IRI 的研究。双氯芬酸降低了氧化平衡,减弱了随后的促炎反应的激活,并减少了细胞和组织损伤。因此,双氯芬酸可能是预防肝 IRI 的有前途的分子。