别嘌呤醇对雄性小鼠肝脏组织病理结构的诱导作用

D. Lestari, Fatimatuzzahra Fatimatuzzahra, Agnes Petra Sianipar, Shahnaz Shabrina Wulansari
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引用次数: 0

摘要

别嘌呤醇用于降低体内总尿酸水平,转化为能抑制黄嘌呤氧化酶的氧嘌呤醇。别嘌呤醇抑制尿酸形成的前体,黄嘌呤和次黄嘌呤。然而,服用这些药物会对肝脏产生副作用。本研究旨在探讨别嘌呤醇对雄性小鼠(小家鼠)肝组织病理学的影响。本研究采用的方法为仅后验的实验设计,分为4组,每组4只。对照组(P0)给予0.5% Na-CMC, I、II、III组(P1、P2、P3)分别以10 mg/kg BW、20 mg/kg BW、30 mg/kg BW剂量的别嘌呤醇诱导14 d。别嘌呤醇诱导采用灌胃法。研究结果显示,别嘌呤醇处理引起小鼠体重、肝脏指数、肝脏形态和肝组织组织学结构的改变,包括坏死、脂肪变性、白细胞浸润、双核肝细胞、肝细胞肿胀、充血、窦状动脉扩张和出血。肝损伤程度随剂量增加而增加。本研究表明,别嘌呤醇含量越高,肝脏切片结构的改变程度越高。长期服用别嘌呤醇可引起小鼠肝脏结构损伤(肝毒性)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Allopurinol Induction on Histopathological Structure of the Liver in Male Mice (Mus musculus)
Allopurinol is used to reduce total uric acid levels in the body into oxypurinol which can inhibit xanthine oxidase. Allopurinol inhibits the precursors of uric acid formation, xanthine, and hypoxanthine. However, consumption of the drugs can cause side effects on the liver. The aim of the research was to determine the effect of allopurinol induction on the liver histopathology of male mice (Mus musculus) DDY strain. The method used in this research was an experimental design used post-test only that was divided into 4 groups of 4 mice per group. The control group (P0) was given 0.5% Na-CMC, and groups I, II, and III (P1, P2, and P3) were induced by allopurinol at 10 mg/kg BW, 20 mg/kg BW, and 30 mg/kg BW for 14 days. Allopurinol induction was performed by oral gavage. The results of the research showed that treatment with allopurinol caused changes in the mice’s body weight, liver index, liver morphology, and histological structure of the liver tissue, including necrosis, steatosis, leukocyte infiltration, binuclear hepatocytes, hepatocyte swelling, congestion, sinusoid dilatation, and hemorrhage. The level of liver damage increased in line with the dose used. This research indicated that the higher the allopurinol level, the higher the level of alteration in the liver section structure. Long-term use of allopurinol can cause damage to the structure of mice liver (liver toxicity). 
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