Departamento de Ciencias Básicas Biomédicas, Facultad de Ciencias de la Salud, Universidad de Talca, Talca 3460000, Chile.
Programa de Doctorado en Ciencias Mención Investigación y Desarrollo de Productos Bioactivos, Instituto de Química de los Recursos Naturales, Universidad de Talca, Talca 3460000, Chile.
Int J Mol Sci. 2020 Nov 22;21(22):8827. doi: 10.3390/ijms21228827.
Liver fibrosis is a complex process associated to most types of chronic liver disease, which is characterized by a disturbance of hepatic tissue architecture and the excessive accumulation of extracellular matrix. Resolvin E1 (RvE1) is a representative member of the eicosapentaenoic omega-3 lipid derivatives, and is a drug candidate of the growing family of endogenous resolvins. Considering the aforementioned, the main objective of this study was to analyze the hepatoprotective effect of RvE1 in a rat model of liver fibrosis. Male Sprague-Dawley rats received diethylnitrosamine (DEN, 70 mg/mg body weight intraperitoneally (i.p)) as an inductor of liver fibrosis once weekly and RvE1(100 ng/body weight i.p) twice weekly for four weeks. RvE1 suppressed the alterations induced by DEN, normalizing the levels of alanine aminotransferase (ALT), albumin, and lactate dehydrogenase (LDH), and ameliorated DEN injury by decreasing the architecture distortion, inflammatory infiltration, necrotic areas, and microsteatosis. RvE1 also limited DEN-induced proliferation through a decrease in Ki67-positive cells and cyclin D1 protein expression, which is related to an increase of the levels of cleaved caspase-3. Interestingly, we found that RvE1 promotes higher nuclear translocation of nuclear factor κB (NF-κB)p65 than DEN. RvE1 also increased the levels of nuclear the nuclear factor erythroid 2-related factor 2 (Nrf2), but with no antioxidant effect, measured as an increase in glutathione disulfide (GSSG) and a decrease in the ratio of glutathione (GSH)/GSSG. Taken together, these results suggest that RvE1 modulates the fibrogenesis, steatosis, and cell proliferation in a model of DEN induced fibrosis.
肝纤维化是一种与大多数慢性肝病相关的复杂过程,其特征是肝组织结构紊乱和细胞外基质过度积累。内源性消退素 E1(RvE1)是二十碳五烯酸ω-3 脂质衍生物的代表性成员,也是内源性消退素不断增加的家族的候选药物。有鉴于此,本研究的主要目的是分析 RvE1 在肝纤维化大鼠模型中的肝保护作用。雄性 Sprague-Dawley 大鼠每周腹腔注射一次二乙基亚硝胺(DEN,70mg/mg 体重)作为肝纤维化诱导剂,每周两次腹腔注射 RvE1(100ng/体重),共 4 周。RvE1 抑制了 DEN 诱导的改变,使丙氨酸氨基转移酶(ALT)、白蛋白和乳酸脱氢酶(LDH)水平正常化,并通过减少结构扭曲、炎症浸润、坏死区和微脂肪变性改善 DEN 损伤。RvE1 还通过降低 Ki67 阳性细胞和细胞周期蛋白 D1 蛋白表达来限制 DEN 诱导的增殖,这与 cleaved caspase-3 水平的增加有关。有趣的是,我们发现 RvE1 促进核因子κB(NF-κB)p65 的核转位高于 DEN。RvE1 还增加了核因子红细胞 2 相关因子 2(Nrf2)的水平,但没有抗氧化作用,表现为谷胱甘肽二硫化物(GSSG)增加和谷胱甘肽(GSH)/GSSG 比值降低。综上所述,这些结果表明 RvE1 调节 DEN 诱导的纤维化模型中的纤维化、脂肪变性和细胞增殖。