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Bioactive properties: enhancement of hepatoprotective, antioxidant and DNA damage protective effects of golden grey mullet protein hydrolysates against paracetamol toxicity

机译:生物活性特性:增强肝保护剂,抗氧化剂和DNA损伤金色灰色Mullet蛋白水解液对扑热氨酸毒性的保护作用

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摘要

This study was undertaken to examine the hepatoprotective, antioxidant, and DNA damage protective effects of protein hydrolysates from Liza aurata, against paracetamol overdose induced liver injury in Wistar rats. L. aurata protein hydrolysates (LAPHs) were mainly constituted by glutamic acid (Glu) and glutamine (Gln) and lysine (Lys). In addition, they contained high amounts of proline (Pro), leucine (Leu) and glycine (Gly). The molecular weight distribution of the hydrolysates was determined by size exclusion chromatography, which analyzed a representative hydrolysate type with a weight range of 3-20 kDa. The hepatoprotective effect of LAPHs against paracetamol liver toxicity was investigated by in vivo assay. Rats received LAPHs daily by gavage, for 45 days. Paracetamol was administrated to rats during the last five days of treatment by intraperitoneal injection. Paracetamol overdose induced marked liver damage in rats was noted by a significant increase in the activities of serum aspartate amino transferase (AST) and alanine amino transferase (ALT), and oxidative stress which was evident from decreased activity of the enzymatic antioxidants (superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx)), and level of glutathione (GSH), and increased concentration of lipid peroxidation products (MDA). Furthermore, paracetamol increased the DNA damage with liver histopathological changes. LAPH pretreatment significantly attenuated paracetamol-induced hepatotoxic effects, including oxidative damage, histopathological lesions, and apoptotic changes in the liver tissue. Interestingly, LAPHs restored the activities of antioxidant enzymes and the level of GSH, ameliorated histological and molecular aspects of liver cells. The present data suggest that paracetamol high-dose plays a crucial role in the oxidative damage and genotoxicity of the liver and therefore, some antioxidants such us LAPHs might be safe as hepatoprotectors. Altogether, our studies provide consistent evidence of the beneficial effect of LAPHs on animals treated with a toxic dose of paracetamol and might encourage clinical trials.
机译:本研究旨在检测肝脏保护剂,抗氧化剂和DNA损伤来自Liza Aurata的蛋白质水解酸盐的保护作用,对抗扑热息醇过量诱导Wistar大鼠的肝损伤。 L. Aurata蛋白质水解产物(Laphs)主要由谷氨酸(glu)和谷氨酰胺(gln)和赖氨酸(Lys)构成。此外,它们含有大量的脯氨酸(Pro),亮氨酸(Leu)和甘氨酸(Gly)。通过尺寸排阻色谱法测定水解产物的分子量分布,其分析了具有3-20kDa的重量范围的代表性水解产物。体内测定研究了Laphs对扑热氨基醇肝毒性的肝保护作用。大鼠每天通过饲喂患者,45天。腹膜内注射期间在治疗的最后五天内给予扑热息痛。甲环酰胺过量诱导大鼠的显着肝脏损伤通过显着增加血清天冬氨酸氨基转移酶(AST)和丙氨酸氨基转移酶(ALT)的活性,以及​​从酶促抗氧化剂(超氧化物歧化酶(所述超氧化物歧化酶)的活性显而易见的氧化应激。 SOD),过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GPX))和谷胱甘肽(GSH)的水平,以及脂质过氧化产物的浓度增加(MDA)。此外,扑热息痛增加了肝脏组织病理学变化的DNA损伤。 Laph预处理显着减弱寄生酵母诱导的肝毒性作用,包括氧化损伤,组织病理病变和肝组织中的凋亡变化。有趣的是,Laphs恢复了抗氧化酶的活性和肝细胞的改善组织学和分子方面的抗氧化剂和GSH水平。本数据表明,扑热息痛高剂量在肝脏的氧化损伤和遗传毒性中起着至关重要的作用,因此,这些美国的抗氧化剂可能是安全的肝脏保护剂。完全,我们的研究提供了一致的证据表明Laphs对用亚乙酰氨基酚毒性剂量治疗的动物的有益效果,并且可能鼓励临床试验。

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  • 来源
    《RSC Advances》 |2018年第41期|共11页
  • 作者单位

    Univ Sfax Natl Sch Engn Sfax ENIS Lab Enzyme Engn &

    Microbiol BP 1173 Sfax 3038 Tunisia;

    Fac Sci Sfax Lab Environm Physiopathol Valorizat Bioact Mol &

    Rd Soukra Km 3-5 PB 1171-14 Sfax 3000 Tunisia;

    Univ Sfax Natl Sch Engn Sfax ENIS Lab Enzyme Engn &

    Microbiol BP 1173 Sfax 3038 Tunisia;

    Fac Sci Sfax Lab Environm Physiopathol Valorizat Bioact Mol &

    Rd Soukra Km 3-5 PB 1171-14 Sfax 3000 Tunisia;

    Fac Sci Sfax Lab Environm Physiopathol Valorizat Bioact Mol &

    Rd Soukra Km 3-5 PB 1171-14 Sfax 3000 Tunisia;

    Univ Sfax Higher Inst Biotechnol Sfax Sfax 3000 Tunisia;

    Univ Sfax Natl Sch Engn Sfax ENIS Lab Enzyme Engn &

    Microbiol BP 1173 Sfax 3038 Tunisia;

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  • 正文语种 eng
  • 中图分类 化学;
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