Department of Pharmacy, 302 Hospital of People's Liberation Army, Beijing, People's Republic of China.
Department of Pharmacy, Xindu District Shibantan Public Hospital, Chengdu, People's Republic of China.
Biomed Pharmacother. 2017 May;89:61-68. doi: 10.1016/j.biopha.2017.02.025. Epub 2017 Feb 17.
Paeoniflorin has shown the obvious effect on cholestasis according to our previous research. However, its mechanism has not been absolutely explored yet. This study aims at evaluating the potential effect of paeoniflorin on alpha-naphthylisothiocyanate (ANIT) -induced cholestasis by inhibiting nuclear factor kappa-B (NF-κB) and simultaneously regulating hepatocyte transporters. Cholestasis was induced by administration of ANIT. The effect of paeoniflorin on serum indices such as total bilirubin (TBIL), direct bilirubin (DBIL), aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), γ-glutamyltranspeptidase (γ-GT), total bile acid (TBA) and histopathology of liver were determined. Liver protein levels of NF-κB, interleukin 1β (IL-1β) and the hepatocyte transporters such as Na/taurocholate cotransporting polypeptide (NTCP), bile salt export pump (BSEP), multidrug resistance-associated protein 2 (MRP2) and cholesterol 7α-hydroxylase (Cyp7a1) were investigated by western blotting. The results demonstrated that paeoniflorin could decrease serum ALT, AST, ALP, γ-GT, TBIL, DBIL and TBA in ANIT-treated rats. Histological examination revealed that rats treated with paeoniflorin represented fewer neutrophils infiltration, edema and necrosis in liver tissue compared with ANIT rats. Moreover, paeoniflorin significantly reduced the over expressions of NF-κB and IL-1β induced by ANIT in liver tissue. In addition, the relative protein expressions of NTCP, BSEP, MRP2 but not Cyp7a1 were also restored by paeoniflorin. The potential mechanism of paeoniflorin in alleviating ANIT-induced cholestasis seems to be related to reduce the over expressions of NF-κB and hepatocyte transporters such as NTCP, BSEP as well as MRP2.
芍药苷先前的研究表明对胆汁淤积具有明显作用。然而,其作用机制尚未完全阐明。本研究旨在通过抑制核因子 kappa-B(NF-κB)并同时调节肝细胞转运体来评估芍药苷对α-萘异硫氰酸酯(ANIT)诱导的胆汁淤积的潜在作用。通过给予 ANIT 诱导胆汁淤积。测定芍药苷对血清总胆红素(TBIL)、直接胆红素(DBIL)、天门冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)、碱性磷酸酶(ALP)、γ-谷氨酰转肽酶(γ-GT)、总胆汁酸(TBA)和肝组织病理学等血清指标的影响。通过 Western blot 法检测肝组织 NF-κB、白细胞介素 1β(IL-1β)和肝细胞转运体如牛磺胆酸钠共转运多肽(NTCP)、胆汁盐输出泵(BSEP)、多药耐药相关蛋白 2(MRP2)和胆固醇 7α-羟化酶(Cyp7a1)的蛋白水平。结果表明,芍药苷可降低 ANIT 处理大鼠的血清 ALT、AST、ALP、γ-GT、TBIL、DBIL 和 TBA。组织学检查显示,与 ANIT 大鼠相比,芍药苷处理的大鼠肝脏组织中中性粒细胞浸润、水肿和坏死减少。此外,芍药苷还显著降低了 ANIT 诱导的肝组织中 NF-κB 和 IL-1β 的过度表达。此外,芍药苷还可恢复 NTCP、BSEP、MRP2 但不是 Cyp7a1 的相对蛋白表达。芍药苷缓解 ANIT 诱导的胆汁淤积的潜在机制似乎与降低 NF-κB 过度表达以及 NTCP、BSEP 和 MRP2 等肝细胞转运体有关。