大叶海葵和非洲海葵的部分。穗青葱。对乙酰氨基酚(APAP)诱导的大鼠肝损伤和线粒体功能障碍的保护作用

Njayou Frederic Nico, M. F. Paul
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引用次数: 0

摘要

目的:探讨桔梗25%二氯甲烷/甲醇(KF25)和非洲藤10%二氯甲烷/甲醇(EF10)预处理对apap诱导的大鼠肝损伤和线粒体功能障碍的影响。材料与方法:动物口服各植物提取物7 d。在剂量反应研究中,以25和100mg/kg体重(b.w)的剂量对这两种组分进行了测试。在线粒体功能障碍研究中,KF25和EF10分别以25和100 mg/kg b.w的剂量给药。两项实验均以水飞蓟海为对照药,剂量为100mg/kg b.w。预处理后,动物口服APAP (1g/kg, b.w)中毒,斩首处死。制备血清、肝脏匀浆和线粒体部分进行生化分析。结果:水飞蓟素、KF25和EF10的保肝率分别为88.65%、86.21%和86.83%,对肝脏脂质过氧化有抑制作用。给药后肝脏还原性谷胱甘肽、超氧化物歧化酶、过氧化氢酶和线粒体复合体(II、III、V)酶活性降低,线粒体肿胀显著改善(P<0.05)。结论:本研究突出了KF25和EF10对apap诱导的肝损伤的保护作用。这些植物馏分可能是治疗药物性肝毒性化合物的良好来源。关键词:桔梗,非洲叶,抑制,线粒体功能障碍,对乙酰氨基酚
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fractions of Khaya grandifoliola C.DC and Entada africana Guill. et Perr. Protect against Acetaminophen (APAP)-induced Liver Damage and Mitochondrial Dysfunction in Rats
Objectives: To investigate the effect of the fractions methylene chloride/methanol 25% (KF25) of K. grandifoliola and 10% (EF10) of E. africana pretreatment against APAP-induced liver damage and mitochondrial dysfunction in rats. Material and Methods: Each plant fraction was orally given to animals for seven days. In dose-response study both fractions were tested at the doses of 25 and 100mg/kg body weight (b.w). In the mitochondria dysfunction study the KF25 and EF10 were administered at 25 and 100 mg/kg b.w, respectively. For both studies, Silymarine was used as reference drug and tested at 100mg/kg b.w. After pretreatment period, animals were intoxicated by oral administration of APAP (1g/kg, b.w) and sacrificed by decapitation. Serum, liver homogenate and mitochondria fraction were prepared for biochemical analyses. Results: Silymarin, KF25 and EF10 exhibited respective percentage of hepatoprotection of 88.65, 86.21 and 86.83% and inhibited liver lipid peroxidation. Levels of liver reduced glutathion, superoxide dismutase, catalase and mitochondrial complexes (II, III and V) enzymes activities decreased upon administration of APAP and mitochondrial swelling were significantly (P<0.05) improved. Conclusions: This study highlights the protective effect of KF25 and EF10 against APAP-induced liver damage. These plant fractions may be good source of compounds for management of drug-induced hepatotoxicity. Key words: Khaya grandifoliola, Entada africana, Inhibition, Mitochondria dysfunction, Acetaminophen.
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