Morphological changes in the liver of experimental animals in the early stages after correction of exposure to high doses of paracetamol

G. V. Timasheva, S. S. Baygildin, A. Bakirov, E. F. Repina, D. Karimov, Nadezhda Yurevna Khusnutdinova, G. F. Mukhammadieva
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Abstract

Introduction. Acetaminophen exhibits hepatotoxicity in overdose, which is the leading cause of drug-induced liver failure. The aim of the research was to study early morphological changes in the liver of experimental animals under the influence of high doses of paracetamol and after correction with hepatoprotectors. Materials and methods. The corrective effect of various drugs - ademetionine, ethylmethylhydroxypyridine succinate and oxymethyluracil after exposure to high doses of acetaminophen was studied. Acetaminophen was administered to experimental rats once intragastrically at a dose of 1 g/kg, animals received hepatoprotectors twice (after 1 and 24 hours) or four times (after 1, 24, 48, 72 hours) after the toxicant. Morphological studies of the liver of experimental animals were carried out. Results. Pathomorphological changes were revealed on rat liver preparations after exposure to paracetamol, the most pronounced after 72 hours of exposure. Oxymethyluracil has a protective effect on the structure of the liver during acute exposure to high doses of paracetamol, comparable to the well-known drugs “Heptor” and “Mexidol”. In addition, the protective effect of oxymethyluracil appears earlier. Limitations. Morphological studies of the liver of 90 white male rats were carried out for studying the corrective action of hepatoprotectors after acute exposure to high doses of acetaminophen and after double (after 1 and 24 hours) or quadruple (after 1, 24, 48, 72 hours) administration of ademethionine, ethylmethylhydroxypyridine succinate and oxymethyluracil, which allowed to determine an effective means to reduce the toxic effect of paracetamol on the liver. Conclusion. The data obtained may have a certain practical value in terms of the prospective use of oxymethyluracil as an additional effective agent for reducing the toxic effect of paracetamol.
实验动物暴露于高剂量扑热息痛后早期肝脏的形态学改变
介绍。对乙酰氨基酚在过量时表现出肝毒性,这是药物性肝衰竭的主要原因。本研究的目的是研究实验动物在高剂量扑热息痛影响下,经肝保护剂纠正后肝脏的早期形态学变化。材料和方法。研究了高剂量对乙酰氨基酚暴露后腺苷、琥珀酸乙基甲基羟吡啶和氧甲基尿嘧啶的矫正效果。实验大鼠对乙酰氨基酚1次灌胃,剂量为1 g/kg,动物在给药后1、24小时或1、24、48、72小时分别给予2次或4次肝保护剂。对实验动物肝脏进行了形态学研究。结果。对乙酰氨基酚暴露后大鼠肝脏组织病理形态学改变,在暴露72小时后最为明显。在急性暴露于高剂量扑热息痛时,氧甲基尿嘧啶对肝脏结构具有保护作用,其作用可与众所周知的药物“Heptor”和“Mexidol”相媲美。此外,氧甲基尿嘧啶的保护作用出现得更早。的局限性。短句来源本研究对90只雄性白种大鼠进行肝脏形态学研究,研究急性高剂量对乙酰氨基酚暴露后,双次(1、24小时)或四次(1、24、48、72小时)给药后肝保护剂的纠正作用,从而确定降低扑热息痛对肝脏毒性作用的有效手段。结论。所获得的数据可能具有一定的实用价值,就未来使用氧甲基尿嘧啶作为减少扑热息痛毒性作用的额外有效剂而言。
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