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乙酰水杨酸和己酮可可碱对非酒精性脂肪性肝炎豚鼠的影响。

The effect of acetylsalicylic acid and pentoxifylline in guinea pigs with non-alcoholic steatohepatitis.

机构信息

Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Frederiksberg C, Denmark.

Liver Disease Research, Global Research, Novo Nordisk A/S, Måløv, Denmark.

出版信息

Basic Clin Pharmacol Toxicol. 2021 Apr;128(4):583-593. doi: 10.1111/bcpt.13549. Epub 2021 Jan 9.

Abstract

Therapeutic options are urgently needed for non-alcoholic fatty liver disease (NAFLD), but development is time-consuming and costly. In contrast, drug repurposing offers the advantages of re-applying compounds that are already approved, thereby reducing cost. Acetylsalicylic acid (ASA) and pentoxifylline (PTX) have shown promise for treatment of NAFLD, but have not yet been tested in combination. Guinea pigs were fed a high-fat diet for 16 weeks and then continued on the diet while being treated with ASA, PTX or ASA+PTX for 8 weeks. Chow-fed animals served as healthy controls. Guinea pigs were CT scanned before intervention start and at intervention end. Animals without steatosis (ie NAFLD) at week 16 were excluded from the data analysis. ASA and PTX alone or in combination did not improve hepatic steatosis, ballooning, inflammation or fibrosis nor did the treatments affect liver enzymes (aminotransferases and alkaline phosphatase) or circulating lipids. Liver triglyceride levels, relative liver weight and hepatic mRNA expression of monocyte chemoattractant protein 1, interleukin 8 and platelet-derived growth factor b were nominally decreased. Thus, in the current study, treatment with ASA and PTX alone or in combination for 8 weeks did not ameliorate NASH or hepatic fibrosis in guinea pigs.

摘要

非酒精性脂肪性肝病 (NAFLD) 急需治疗选择,但开发过程既耗时又昂贵。相比之下,药物再利用具有重新应用已批准的化合物的优势,从而降低成本。乙酰水杨酸 (ASA) 和己酮可可碱 (PTX) 已显示出治疗 NAFLD 的潜力,但尚未联合测试。将高脂肪饮食喂养给豚鼠 16 周,然后继续用该饮食喂养,同时用 ASA、PTX 或 ASA+PTX 治疗 8 周。以普通饮食喂养的动物作为健康对照组。在干预开始前和干预结束时对豚鼠进行 CT 扫描。在第 16 周没有脂肪变性(即 NAFLD)的动物被排除在数据分析之外。ASA 和 PTX 单独或联合使用均不能改善肝脂肪变性、气球样变、炎症或纤维化,也不能影响肝酶(氨基转移酶和碱性磷酸酶)或循环脂质。肝甘油三酯水平、相对肝重和单核细胞趋化蛋白 1、白细胞介素 8 和血小板衍生生长因子 b 的肝 mRNA 表达均有降低。因此,在本研究中,8 周内单独或联合使用 ASA 和 PTX 治疗并未改善豚鼠的 NASH 或肝纤维化。

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