两种L-肉碱制剂的比较分析及其浓度对健康人外周血淋巴细胞CAT表达的影响

M. Kuzmanović, N. Lojo-Kadrić, J. Ramic, A. Haverić, S. Haverić, L. Pojskic
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引用次数: 0

摘要

CAT基因编码过氧化氢酶,过氧化氢酶是人体对抗氧化应激的关键抗氧化酶。该酶在炎症、细胞凋亡、突变和肿瘤发生的分子机制中起重要作用。抗氧化剂左旋肉碱用于食品补充,医疗辅助治疗和体重调节。本研究旨在通过体外定制CAT基因检测,探讨左旋肉碱商业制剂降低氧化应激的分子基础。用标准程序建立了人淋巴细胞培养,并在两种制剂中用一定浓度的左旋肉碱处理。我们测试了两种制剂:500毫克的左旋肉碱片剂和含有维生素B6的液体左旋肉碱。与阴性对照相比,50 μmol/l和250 μmol/l浓度的左旋肉碱显著降低了培养淋巴细胞中CAT基因的表达(p = 0.001;P = 0.001;分别)。与阴性对照相比,添加维生素B6的左旋肉碱液体在浓度为50 μmol/l和250 μmol/l时也降低了CAT基因的转录(p = 0,018;P = 0.006;分别)。选定的左旋肉碱制剂可调节人淋巴细胞培养中抗氧化酶基因的转录活性,表明其可能抑制涉及过氧化氢酶活性的促炎过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative analysis of two L-carnitine preparations and their concentration effects on CAT expression in healthy human peripheral blood lymphocyte cultures
CAT gene encodes catalase, a key antioxidant enzyme in the body against oxidative stress. This enzyme plays an important role in the molecular mechanisms of inflammation, apoptosis, mutagenesis and tumorigenesis. Anti-oxidant L-carnitine is used in food supplementation, medical co-treatment and bodyweight regulation. We aimed to investigate molecular basis of L-carnitine commercial preparations supplementation in reducing oxidative stress with customized CAT gene assay in vitro. Human lymphocytes cell culture was established using standard procedure and treated with range of concentrations of L-carnitine in two preparations. We tested two preparations: 500 mg tablets of L-carnitine and liquid L-carnitine with vitamin B6. L-carnitine significantly reduced the expression of CAT gene in cultured lymphocytes at concentrations of 50 μmol/l and 250 μmol/l compared to negative control, (p = 0,001; p = 0,001; respectively). The L-carnitine liquid supplement with vitamin B6 also reduced the transcription of CAT gene at concentrations of 50 μmol/l and 250 μmol/l as compared to the negative control (p = 0,018; p = 0,006; respectively). Selected L-carnitine preparations modulated the transcriptional activity of the antioxidant enzyme gene in human lymphocyte culture, indicating its possible effects in inhibition of pro-inflammatory processes that involve catalase activity.
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