Son Young-Ok, Hwang Jung-Min, Choi Ki-Choon, Lee Jeong-Chae
1Cell Dynamics Research Center and School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju, 61005 South Korea.
2Research Center of Bioactive Materials, Institute of Oral Biosciences and School of Dentistry, Chonbuk National University, Jeonju, 54896 South Korea.
Indian J Clin Biochem. 2019 Jan;34(1):68-75. doi: 10.1007/s12291-017-0714-x. Epub 2017 Dec 2.
The aims of this study were to explore whether a phenolic acid and flavonoid fraction (named PAFF) isolated from Lam. protects against d-galactosamine (GalN)-induced liver damages in mice and to investigate the associated mechanisms. ICR mice received oral administration with various concentrations (50, 100, and 200 mg/kg body weight) of PAFF once per 2 days for seven times before intraperitoneal injection with 800 mg/kg GalN. After a day of GalN challenge, blood and tissue samples were analyzed by biochemical, histopathological, real time RT-PCR, and Western blot methods. GalN challenge induced severe damage to hepatocytes with hepatocellular vacuolization and necrosis. GalN treatment increased serum ALT, ALP, AST, and LDH levels and hepatic MDA levels and stimulated mRNA and protein expressions of Nrf2 and HO-1 in the liver. GalN treatment also diminished the levels of GSH and the activities of CAT, SOD, and GPx in the liver. However, combined treatment with PAFF inhibited GalN-mediated increases in the histological damages and the levels of serum enzymes and hepatic MDA, restored the activities of hepatic antioxidant enzymes up to those in the control values, and augmented the GalN-stimulated expression of Nrf2 and HO-1 in the liver. Furthermore, PAFF treatment alone increased the cellular SOD activity and the expression of Nrf2 and HO-1 in the liver. Our results suggest that PAFF may protect against GalN-induced liver damage by decreasing oxidative stress and increasing cellular antioxidant activities through an activation of Nrf2/HO-1-dependent pathway.
本研究的目的是探讨从[植物名称未给出]中分离得到的酚酸和黄酮类组分(命名为PAFF)是否能保护小鼠免受D-半乳糖胺(GalN)诱导的肝损伤,并研究其相关机制。ICR小鼠每2天口服一次不同浓度(50、100和200mg/kg体重)的PAFF,共7次,然后腹腔注射800mg/kg GalN。在GalN攻击一天后,通过生化、组织病理学、实时RT-PCR和蛋白质印迹法分析血液和组织样本。GalN攻击导致肝细胞严重损伤,出现肝细胞空泡化和坏死。GalN处理增加了血清ALT、ALP、AST和LDH水平以及肝脏MDA水平,并刺激了肝脏中Nrf2和HO-1的mRNA和蛋白质表达。GalN处理还降低了肝脏中GSH水平以及CAT、SOD和GPx的活性。然而,PAFF联合处理抑制了GalN介导的组织学损伤增加以及血清酶和肝脏MDA水平,将肝脏抗氧化酶的活性恢复到对照值水平,并增强了GalN刺激的肝脏中Nrf2和HO-1的表达。此外,单独使用PAFF处理增加了肝脏中细胞SOD活性以及Nrf2和HO-1的表达。我们的结果表明,PAFF可能通过激活Nrf2/HO-1依赖性途径降低氧化应激并增加细胞抗氧化活性,从而保护小鼠免受GalN诱导的肝损伤。