首页> 外文期刊>ACS Omega >Protective Effects of Rice Peptide Oryza Peptide-P60 against Oxidative Injury through Activation of Nrf2 Signaling Pathway In Vitro and In Vivo
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Protective Effects of Rice Peptide Oryza Peptide-P60 against Oxidative Injury through Activation of Nrf2 Signaling Pathway In Vitro and In Vivo

机译:水稻肽Oryza肽-P60通过在体外和体内激活NRF2信号通路激活氧化损伤的保护作用

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We previously showed that commercially available rice peptide Oryza Peptide-P60 (OP60) increased the intracellular glutathione levels. This study aimed to evaluate the antioxidant potential of this peptide and assess its mechanism of action. Pretreatment of HepG2 cells with OP60 reduced the cytotoxicity caused by H_(2)O_(2) or acetaminophen (APAP) (47.7 ± 1.3% or 12.2 ± 1.3% of the cytotoxicity for 5 mg/mL OP60 pretreatment compared to that in H_(2)O_(2)- or APAP-treated groups, respectively; p < 0.01) through the restoration of glutathione homeostasis. Moreover, OP60 elevated the mRNA level of genes encoding heavy and light subunits of γ-glutamylcysteine synthetase (γ-GCS) by 2.9 ± 0.1-fold and 2.7 ± 0.2-fold (p < 0.001), respectively, at 8 h and also increased the level of mRNA encoding other antioxidant enzymes. Besides, OP60 promoted Nrf2 nuclear translocation by 2.2 ± 0.3-fold (p < 0.05) after 8 h. Conversely, knockdown of Nrf2 inhibited the increase of the intracellular glutathione levels and suppressed the induction of antioxidant enzyme expression by OP60. In animal studies, OP60 prevented APAP-induced liver injury by suppressing glutathione depletion (from 0.19 ± 0.02 mmol/mg protein to 0.90 ± 0.02 mmol/mg protein; p < 0.01, by pretreatment with 500 mg/kg OP60) and increasing heavy subunit of γ-GCS and heme oxygenase-1 expression in the liver. Our results indicated that OP60 exhibits a cytoprotective effect via the Nrf2 signaling pathway and is one of the few peptides with excellent antioxidant properties.
机译:我们以前表明市售的水稻肽Oryza肽-P60(OP60)增加了细胞内谷胱甘肽水平。本研究旨在评估该肽的抗氧化潜力并评估其作用机制。用OP60的HEPG2细胞的预处理降低了由H_(2)O_(2)或乙酰氨基酚(APAP)引起的细胞毒性(47.7±1.3%或12.2±1.3%的细胞毒性为5mg / ml OP60预处理( 2)O_(2) - 或APAP治疗组分别; P <0.01)通过谷胱甘肽稳态恢复。此外,OP60分别升高了将γ-谷氨酸琥珀酰基合成酶(γ-GCS)的重和光亚基的基因的mRNA水平分别在8小时内分别在2.9±0.1倍和2.7±0.2倍( p <0.001)中并且还增加编码其他抗氧化酶的mRNA水平。此外,OP60在8小时后通过2.2±0.3倍( P <0.05)促进NRF2核易位。相反,NRF2的敲低抑制了细胞内谷胱甘肽水平的增加,并抑制了OP60的抗氧化酶表达的诱导。在动物研究中,OP60通过抑制谷胱甘肽耗尽(从0.19±0.02mmol / mg蛋白至0.90±0.02mmol / mg / mg蛋白质来预防APAP诱导的肝损伤; P <0.01,通过预处理500mg / kg OP60)和肝脏中增加γ-GCS和血红素氧酶-1表达的重亚基。我们的结果表明,OP60通过NRF2信号通路表现出细胞保护作用,是少量抗氧化性能的肽之一。

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