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己酮可可碱可减轻蛋氨酸胆碱缺乏饮食诱导的脂肪性肝炎。

Pentoxifylline attenuates steatohepatitis induced by the methionine choline deficient diet.

作者信息

Koppe Sean W P, Sahai Atul, Malladi Padmini, Whitington Peter F, Green Richard M

机构信息

Department of Medicine, Division of Hepatology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.

出版信息

J Hepatol. 2004 Oct;41(4):592-8. doi: 10.1016/j.jhep.2004.06.030.

Abstract

BACKGROUND/AIMS: Feeding mice a methionine choline deficient (MCD) diet serves as a nutritional model of non-alcoholic steatohepatitis (NASH). NASH and alcohol-induced steatohepatitis are histologically similar, suggesting a similar pathogenesis. Pentoxifylline (PTX) attenuates TNF-alpha production, acts as an antioxidant and decreases mortality in alcoholic steatohepatitis. The aim of our study is to determine if PTX attenuates MCD diet induced steatohepatitis and determine the mechanism of this effect.

METHODS

Mice were placed on an MCD or control diet for 2 weeks and were treated with or without PTX. Serum ALT, liver histology, and inflammatory mechanisms were evaluated.

RESULTS

PTX attenuates MCD diet induced steatohepatitis, decreasing both serum ALT levels and hepatic inflammation. Serum ALT levels were reduced approximately 50% in the MCD+PTX group compared to the MCD group. Hepatic glutathione levels were significantly higher in the MCD+PTX group compared to the MCD group. There was also a reduction in TNF-alpha mRNA in female mice treated with PTX. MCD+PTX mice had increased hepatic triglyceride content compared to the MCD mice, but less histologic evidence of inflammation despite the increased steatosis. Serum lipid and bile salt levels also were similar in PTX and vehicle control treated mice.

CONCLUSIONS

PTX decreases serum ALT levels and hepatic inflammation in the MCD model of steatohepatitis, likely via increasing glutathione levels or reducing TNF-alpha expression.

摘要

背景/目的:给小鼠喂食蛋氨酸胆碱缺乏(MCD)饮食可作为非酒精性脂肪性肝炎(NASH)的营养模型。NASH与酒精性脂肪性肝炎在组织学上相似,提示发病机制相似。己酮可可碱(PTX)可减少肿瘤坏死因子-α(TNF-α)生成,具有抗氧化作用,并可降低酒精性脂肪性肝炎的死亡率。本研究旨在确定PTX是否可减轻MCD饮食诱导的脂肪性肝炎,并确定其作用机制。

方法

将小鼠分为MCD饮食组或对照组,喂养2周,分别给予或不给予PTX治疗。评估血清丙氨酸氨基转移酶(ALT)、肝脏组织学及炎症机制。

结果

PTX可减轻MCD饮食诱导的脂肪性肝炎,降低血清ALT水平及肝脏炎症。与MCD组相比,MCD+PTX组血清ALT水平降低约50%。与MCD组相比,MCD+PTX组肝脏谷胱甘肽水平显著升高。给予PTX治疗的雌性小鼠TNF-α mRNA水平也降低。与MCD小鼠相比,MCD+PTX小鼠肝脏甘油三酯含量增加,但尽管脂肪变性增加,炎症的组织学证据较少。PTX组和溶剂对照组小鼠的血清脂质和胆汁盐水平也相似。

结论

在脂肪性肝炎的MCD模型中,PTX可能通过提高谷胱甘肽水平或降低TNF-α表达来降低血清ALT水平及肝脏炎症。

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