Reduction of hepatotoxicity of nimesulide in mechanochemically obtained composition with disodium salt of glycyrrhizic acid

Q4 Biochemistry, Genetics and Molecular Biology
E. S. Petrova, N. A. Zhukova, V. Evseenko, M. Khvostov, I. V. Meshkova, T. Tolstikova, A. Dushkin
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Abstract

Nimesulide (NIM) is a nonsteroid anti-inflammatory drug which acts as a selective cyclooxygenase 2 inhibitor and is widely used for acute pain treatment. In medical practice, a large amount of data has been collected describing the effect of NIM on the body, while a hepatotoxic side effect of the drug has been found. The exact mechanisms of such NIM-induced hepatotoxicity largely remain unknown but likely involve the intermediate reaction of its metabolism. Reduction of the hepatotoxic side effect of NIM is an actual problem for pharmacology. The aim of the present research was to evaluate the hepatotoxicity of the mechanochemically obtained composition of NIM with glycyrrhizic acid disodium salt (Na2GA) compared to pure NIM and a physical mixture of NIM with Na2GA. Material and methods. CD-1 mice were orally administered for 14 days: 1 group – mechanochemical composition NIM/Na2GA (1:10, m/m) at a dose of 1650 mg/kg; 2 group – physical mixture of NIM with Na2GA (1:10, m/m) at a dose of 1650 mg/kg; 3 group – pure NIM at a dose of 600 mg/kg (which pharmacokinetically corresponds to 1650 mg/kg of NIM/Na2GA); 4 group – vehicle (distilled water). The liver damage was assessed using histological studies and enzymatic activity of the alanine aminotransferase and aspartate aminotransferase in blood serum. Results. Histological analysis did not detect any changes in the liver of NIM/Na2GA-treated animals in comparison with a water-treated group. On the opposite, NIM given alone or as a physical mixture with Na2GA induced severe hepatotoxicity in experimental mice. Biochemical analysis of the blood serum revealed that mechanochemical NIM/Na2GA composition significantly reduced activity of the alanine aminotransferase (about 1.5 times) and aspartate aminotransferase (1.3 times) as compared with the pure NIM. Conclusions. The results obtained indicate a high potential for the practical application of the NIM/Na2GA mechanochemical composition.
用甘草酸二钠盐机械化学合成的尼美舒利降低肝毒性
尼美舒利(Nimesulide, NIM)是一种非甾体抗炎药,作为选择性环加氧酶2抑制剂,广泛用于急性疼痛治疗。在医疗实践中,已经收集了大量的数据来描述NIM对人体的影响,同时也发现了该药物的肝毒性副作用。这种nim诱导的肝毒性的确切机制在很大程度上仍不清楚,但可能涉及其代谢的中间反应。降低NIM的肝毒副作用是药理学研究的现实问题。本研究的目的是评价机械化学合成的NIM与甘草酸二钠盐(Na2GA)的组合物与纯NIM和NIM与Na2GA的物理混合物的肝毒性。材料和方法。CD-1小鼠口服14 d:1组-机械化学成分NIM/Na2GA (1:10, m/m),剂量为1650 mg/kg;2组:NIM与Na2GA物理混合(1:10,m/m),剂量为1650 mg/kg;3组-纯NIM剂量为600 mg/kg(药代动力学对应于1650 mg/kg NIM/Na2GA);4组-车辆(蒸馏水)。通过组织学研究和血清中丙氨酸转氨酶和天冬氨酸转氨酶的酶活性来评估肝损伤。结果。与水处理组相比,组织学分析未发现NIM/ na2ga处理的动物肝脏有任何变化。相反,NIM单独给药或与Na2GA物理混合给药对实验小鼠产生严重的肝毒性。血清生化分析表明,与纯NIM相比,机械化学NIM/Na2GA组分显著降低了丙氨酸转氨酶(约1.5倍)和天冬氨酸转氨酶(约1.3倍)的活性。结论。研究结果表明,NIM/Na2GA力学化学成分具有很大的应用潜力。
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来源期刊
CiteScore
0.40
自引率
0.00%
发文量
54
审稿时长
12 weeks
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