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甘草根通过抑制蛋白质硝化减轻过氧亚硝酸盐诱导的肾脏氧化损伤。

Glycyrrhizae Radix attenuates peroxynitrite-induced renal oxidative damage through inhibition of protein nitration.

作者信息

Yokozawa Takako, Cho Eun Ju, Rhyu Dong Young, Shibahara Naotoshi, Aoyagi Kazumasa

机构信息

Institute of Natural Medicine, Toyama Medical and Pharmaceutical University, Toyama 930-0194, Japan.

出版信息

Free Radic Res. 2005 Feb;39(2):203-11. doi: 10.1080/10715760400027888.

Abstract

We investigated the protective effects of Glycyrrhizae Radix extract against peroxynitrite (ONOO-)-induced oxidative stress under in vivo as well as in vitro conditions. The extract showed strong ONOO- and nitric oxide (NO) scavenging effects under in vitro system, in particular higher activity against ONOO-. Furthermore, elevations of plasma 3-nitrotyrosine levels, indicative of in vivo ONOO- generation and NO production, were shown using a rat in vivo ONOO(-)-generation model of lipopolysaccharide injection plus ischemia-reperfusion. The administration of Glycyrrhizae Radix extract at doses of 30 and 60 mg/kg body weight/day for 30 days significantly reduced the concentrations of 3-nitrotyrosine and NO and decreased inducible NO synthase activity. In addition, the nitrated tyrosine protein level and myeloperoxidase activity in the kidney were significantly lower in rats given Glycyrrhizae Radix extract than in control rats. However, the administration of Glycyrrhizae Radix extract did not result in either significant elevation of glutathione levels or reduction of lipid peroxidation in renal mitochondria. Moreover, the in vivo ONOO- generation system resulted in renal functional impairment, reflected by increased plasma levels of urea nitrogen and creatinine, whereas the administration of Glycyrrhizae Radix extract reduced these levels significantly, implying that the renal dysfunction induced by ONOO- was ameliorated. The present study suggests that Glycyrrhizae Radix extract could protect the kidneys against ONOO- through scavenging ONOO- and/or its precursor NO, inhibiting protein nitration and improving renal dysfunction caused by ONOO-.

摘要

我们研究了甘草提取物在体内和体外条件下对过氧亚硝酸根(ONOO⁻)诱导的氧化应激的保护作用。在体外系统中,该提取物表现出强大的ONOO⁻和一氧化氮(NO)清除作用,尤其是对ONOO⁻具有更高的活性。此外,使用脂多糖注射加缺血再灌注的大鼠体内ONOO⁻生成模型,显示血浆3-硝基酪氨酸水平升高,这表明体内有ONOO⁻生成和NO产生。以30和60 mg/kg体重/天的剂量给予甘草提取物30天,可显著降低3-硝基酪氨酸和NO的浓度,并降低诱导型NO合酶活性。此外,给予甘草提取物的大鼠肾脏中硝化酪氨酸蛋白水平和髓过氧化物酶活性明显低于对照大鼠。然而,给予甘草提取物并未导致肾线粒体中谷胱甘肽水平显著升高或脂质过氧化减少。此外,体内ONOO⁻生成系统导致肾功能损害,表现为血浆尿素氮和肌酐水平升高,而给予甘草提取物可显著降低这些水平,这意味着ONOO⁻诱导的肾功能障碍得到改善。本研究表明,甘草提取物可通过清除ONOO⁻和/或其前体NO、抑制蛋白质硝化以及改善ONOO⁻引起的肾功能障碍来保护肾脏免受ONOO⁻的损伤。

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