State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, 1 Keyuan Road 4, Chengdu, Sichuan 610041, China.
J Pharmacol Exp Ther. 2012 Apr;341(1):146-55. doi: 10.1124/jpet.111.189498. Epub 2012 Jan 11.
Acute liver failure (ALF) is a relatively rare liver disorder that leads to the massive death of hepatocytes. Our previous study reported that a novel small-molecule agent, (E)-5-(2,4-di-tert-butyl-6-((2,4-dioxothiazolidin-5-ylidene)methyl)phenyl)-5'-methyl-7,7'-dimethoxy-4,4'-bibenzo[d][1,3]dioxole-5,5'-dicarboxylate (7k), possessed potent anti-inflammatory activity. In the present study, we further evaluated the therapeutic effects of 7k on lipopolysaccharide (LPS)-induced ALF and investigated the mechanisms of action. Our results demonstrated that 7k inhibited the migration of RAW264.7 macrophages, blocked the activity of nuclear factor-κB protein, and dose-dependently down-regulated the production of interleukin (IL)-1β, tumor necrosis factor-α, and IL-6 as well as their corresponding mRNAs in RAW264.7 cells. Oral administration of 7k at a dose of 50 mg/kg significantly suppressed the serum level of enzyme activity and prevented the damage of liver tissue in D-galactosamine/LPS-induced ALF. Treatment with 7k also remarkably blocked the increase in the number of CD11b(+)- and CD68(+)-positive cells in the liver, and in vivo nuclear factor-κB activity, known to regulate inflammatory responses in many cell types, was effectively inhibited. The serum concentrations and hepatic mRNA expression of proinflammatory cytokines tumor necrosis factor-α, IL-1β, and IL-6 were markedly down-regulated in mice by the treatment of 7k. In summary, 7k alleviated the development and progression of D-galactosamine/LPS-induced ALF by inhibiting macrophage infiltration and regulating the expression of cytokines.
急性肝衰竭(ALF)是一种相对罕见的肝脏疾病,可导致大量肝细胞死亡。我们之前的研究报告称,一种新型小分子药物(E)-5-(2,4-二叔丁基-6-((2,4-二氧代噻唑烷-5-亚基)甲基)苯基)-5'-甲基-7,7'-二甲氧基-4,4'-联苯并[d][1,3]二恶唑-5,5'-二羧酸酯(7k)具有很强的抗炎活性。在本研究中,我们进一步评估了 7k 对脂多糖(LPS)诱导的 ALF 的治疗作用,并研究了其作用机制。结果表明,7k 抑制 RAW264.7 巨噬细胞的迁移,阻断核因子-κB 蛋白的活性,并呈剂量依赖性地下调 RAW264.7 细胞中白细胞介素(IL)-1β、肿瘤坏死因子-α 和 IL-6 及其相应 mRNA 的产生。50mg/kg 的 7k 口服剂量可显著抑制酶活性的血清水平,并防止 D-半乳糖胺/LPS 诱导的 ALF 中肝组织的损伤。7k 的治疗还显著阻止了肝脏中 CD11b(+)-和 CD68(+)-阳性细胞数量的增加,并且体内核因子-κB 活性(已知可调节许多细胞类型的炎症反应)也得到有效抑制。7k 治疗可显著下调 TNF-α、IL-1β 和 IL-6 等促炎细胞因子的血清浓度和肝组织 mRNA 表达。综上所述,7k 通过抑制巨噬细胞浸润和调节细胞因子表达来缓解 D-半乳糖胺/LPS 诱导的 ALF 的发展和进展。