首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >Antiapoptotic effect of a novel synthetic peptide from bovine muscle and MPG peptide on H2O2-induced C2C12 cells
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Antiapoptotic effect of a novel synthetic peptide from bovine muscle and MPG peptide on H2O2-induced C2C12 cells

机译:牛肌肉新合成肽和MPG肽对H2O2诱导的C2C12细胞的抗凋亡作用

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The objective of this study was to evaluate antioxidant and antiapoptotic effects of a novel peptide (T.peptide) isolated from bovine and commercially available MPG peptide. The amino acid sequences of the T.peptide were (Glu-Val-Pro-Glu-Val-His-Glu-Glu-Val). The antioxidant activities of these peptides were determined by measuring the 1,1-diphenyl-2-picrylhydrazyl (DPPHaEuro cent) and 2,2'-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) (ABTS+aEuro cent) radical scavenging assays. The in vitro cytotoxicity of T.peptide and MPG peptide was determined against H2O2-induced C2C12 cells. H2O2-induced apoptosis in C2C12 cells were determined by mRNA expression of caspase-3. Moreover, the mRNA expression of tumor necrosis factor alpha (TNF-alpha) and nuclear factor kappa B (NF-kappa B) were assayed by reverse transcription polymerase chain reaction. The findings of the study indicate that the mRNA expression of TNF-alpha and NF-kappa B are significantly (p 0.05) increased in H2O2-induced C2C12 cells, whereas a significant decrease (p 0.05) in these mRNA expressions are observed when pretreated with T.peptide or MPG peptide. Pretreatment with MPG or T.peptides is also found to significantly (p 0.05) decrease the mRNA expression of caspase-3 in H2O2-induced C2C12 cells. The results of the study demonstrate that both T.peptide and MPG peptide could reduce the DPPHaEuro cent and ABTS+aEuro cent radical and inhibit cytotoxicity against H2O2-induced injury, resulting in prevention of free radical generation and subsequent apoptotic cell death, which indicates the potential of bovine meat as a source of antioxidant peptides.
机译:这项研究的目的是评估从牛和市售MPG肽中分离得到的新型肽(T.peptide)的抗氧化和抗凋亡作用。 T.肽的氨基酸序列是(Glu-Val-Pro-Glu-Val-His-Glu-Glu-Val)。这些肽的抗氧化活性是通过测量1,1-二苯基-2-吡啶甲基肼基(DPPHaEuro cent)和2,2'-叠氮基双(3-乙基苯并噻唑啉-6-磺酸)(ABTS + aEuro cent)自由基来确定的清除测定。测定了T.肽和MPG肽对H2O2诱导的C2C12细胞的体外细胞毒性。通过caspase-3 mRNA表达确定H2O2诱导的C2C12细胞凋亡。此外,通过逆转录聚合酶链反应测定了肿瘤坏死因子α(TNF-α)和核因子κB(NF-κB)的mRNA表达。研究结果表明,在H2O2诱导的C2C12细胞中,TNF-α和NF-κB的mRNA表达显着增加(p <0.05),而当H2O2诱导的C2C12细胞时,这些mRNA表达显着降低(p <0.05)。用T.peptide或MPG肽预处理。还发现用MPG或T.肽进行预处理可显着(p <0.05)降低H2O2诱导的C2C12细胞中caspase-3的mRNA表达。研究结果表明,T。肽和MPG肽均可降低DPPHaEuro分和ABTS + aEuro分,并抑制针对H2O2诱导的损伤的细胞毒性,从而阻止了自由基的产生和随后的凋亡性细胞死亡。牛肉作为抗氧化剂肽来源的潜力。

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