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-吡啶并肼基(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的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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