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绿茶提取物对铜纳米颗粒诱导大鼠肝毒性的改善作用。

Ameliorative Influence of Green Tea Extract on Copper Nanoparticle-Induced Hepatotoxicity in Rats.

机构信息

Department of Biochemistry and Chemistry of Nutrition, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.

Department of Forensic Medicine and Toxicology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.

出版信息

Nanoscale Res Lett. 2015 Dec;10(1):363. doi: 10.1186/s11671-015-1068-z. Epub 2015 Sep 16.

Abstract

The potential toxicity of copper nanoparticles (CNPs) to the human health and environment remains a critical issue. In the present study, we investigated the protective influence of an aqueous extract of green tea leaves (GTE) against CNPs-induced (20-30 nm) hepatotoxicity. Four different groups of rats were used: group I was the control, group II received CNPs (40 mg/kg BW), group III received CNPs plus GTE, and group IV received GTE alone. We highlighted the hepatoprotective effect of GTE against CNPs toxicity through monitoring the alteration of liver enzyme activity, antioxidant defense mechanism, histopathological alterations, and DNA damage evaluation. The rats that were given CNPs only had a highly significant elevation in liver enzymes, alteration in oxidant-antioxidant balance, and severe pathological changes. In addition, we detected a significant elevation of DNA fragmentation percentage, marked DNA laddering, and significance over expression of both caspase-3 and Bax proteins. The findings for group III clarify the efficacy of GTE as a hepatoprotectant on CNPs through improving the liver enzyme activity, antioxidant status, as well as suppressing DNA fragmentation and the expression of the caspase-3 and Bax proteins. In conclusion, GTE was proved to be a potential hepatoprotective additive as it significantly ameliorates the hepatotoxicity and apoptosis induced by CNPs.

摘要

铜纳米粒子(CNPs)对人类健康和环境的潜在毒性仍然是一个关键问题。在本研究中,我们研究了绿茶提取物(GTE)对 CNPs 诱导的(20-30nm)肝毒性的保护作用。使用了四组不同的大鼠:第 I 组为对照组,第 II 组给予 CNPs(40mg/kg BW),第 III 组给予 CNPs 加 GTE,第 IV 组给予 GTE 单独处理。我们通过监测肝酶活性、抗氧化防御机制、组织病理学改变和 DNA 损伤评估,突出了 GTE 对 CNPs 毒性的保护作用。只给予 CNPs 的大鼠的肝酶显著升高,氧化还原平衡发生改变,病理变化严重。此外,我们还检测到 DNA 片段化百分比显著升高,明显的 DNA 梯状带,以及 caspase-3 和 Bax 蛋白的表达显著增加。第 III 组的结果表明,GTE 通过改善肝酶活性、抗氧化状态以及抑制 DNA 片段化和 caspase-3 和 Bax 蛋白的表达,作为一种肝保护剂对 CNPs 具有疗效。总之,GTE 被证明是一种潜在的肝保护添加剂,因为它显著改善了由 CNPs 诱导的肝毒性和细胞凋亡。

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