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镁钙尿囊素对 D-半乳糖胺诱导的大鼠肝毒性的保护作用。

Protective effects of Mg-CUD against D-galactosamine-induced hepatotoxicity in rats.

机构信息

School of Pharmacy, Sungkyunkwan University, 300 Cheoncheon-dong, Jangan-gu, Suwon, Gyeonggi-do 440-746, Republic of Korea.

出版信息

Eur J Pharmacol. 2011 Apr 25;657(1-3):138-43. doi: 10.1016/j.ejphar.2011.01.030. Epub 2011 Jan 31.

DOI:10.1016/j.ejphar.2011.01.030
PMID:21284943
Abstract

This study examined the protective effects of magnesium chenoursodeoxycholic acid (Mg-CUD), a magnesium trihydrate salt of chenodeoxycholic acid (CDCA) and ursodeoxycholic acid (UDCA), against D-galactosamine (D-GalN)-induced liver injury. Hepatotoxicity was induced by intraperitoneal injection of D-GalN (700mg/kg) and Mg-CUD (15.625, 31.25 and 62.5mg/kg) was administered orally once a day for 2weeks and 6h after D-GalN injection. Significant increases in the level of serum alanine aminotransferase activity and lipid peroxidation were attenuated by Mg-CUD 24h after D-GalN treatment. Hepatic glutathione/oxidized glutathione ratio was decreased, and this decrease was attenuated by Mg-CUD. Mg-CUD attenuated the increase in the levels of serum tumor necrosis factor (TNF)-α and interleukin (IL)-6, while it augmented the increase in serum IL-10 level and heme oxygenase (HO)-1 protein expression. Mg-CUD attenuated increased levels of TNF-α, IL-6, and IL-1β mRNA expression. Increased levels of IL-10 and HO-1 mRNA expression were augmented by Mg-CUD. The increased nuclear level of nuclear factor-κB (NF-κB) and decreased cytosolic level of Inhibitory κB-α protein were attenuated by Mg-CUD. Nuclear phosphorylated c-Jun (p-c-Jun) level showed a significant increase and this increase was attenuated by Mg-CUD. Our results suggest that Mg-CUD ameliorates D-GalN-induced acute hepatitis and that this protection is likely due to its anti-oxidative and anti-inflammatory activities, and inhibition of NF-κB nuclear translocation and nuclear p-c-Jun expression.

摘要

本研究考察了镁熊去氧胆酸(Mg-CUD)对 D-半乳糖胺(D-GalN)诱导的肝损伤的保护作用。采用腹腔注射 D-GalN(700mg/kg)诱导肝毒性,Mg-CUD(15.625、31.25 和 62.5mg/kg)每天口服给药一次,在 D-GalN 注射后 2 周和 6 小时给药。Mg-CUD 可减轻 D-GalN 处理后 24 小时血清丙氨酸氨基转移酶活性和脂质过氧化水平的显著升高。肝组织谷胱甘肽/氧化型谷胱甘肽比值降低,Mg-CUD 可减轻这种降低。Mg-CUD 可减轻血清肿瘤坏死因子(TNF)-α和白细胞介素(IL)-6 水平的升高,同时增加血清 IL-10 水平和血红素加氧酶(HO)-1 蛋白表达。Mg-CUD 可减轻 TNF-α、IL-6 和 IL-1βmRNA 表达水平的升高。Mg-CUD 可增加 IL-10 和 HO-1 mRNA 表达水平。Mg-CUD 可减轻核因子-κB(NF-κB)核内水平的升高和胞质内抑制κB-α蛋白水平的降低。核磷酸化 c-Jun(p-c-Jun)水平显著升高,Mg-CUD 可减轻这种升高。我们的结果表明,Mg-CUD 可改善 D-GalN 诱导的急性肝炎,这种保护作用可能与其抗氧化和抗炎活性以及抑制 NF-κB 核转位和核 p-c-Jun 表达有关。

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