首页> 外文期刊>Archives of Biochemistry and Biophysics >Prevention by L-carnitine of DNA damage induced by 3-hydroxy-3-methylglutaric and 3-methylglutaric acids and experimental evidence of lipid and DNA damage in patients with 3-hydroxy-3-methylglutaric aciduria
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Prevention by L-carnitine of DNA damage induced by 3-hydroxy-3-methylglutaric and 3-methylglutaric acids and experimental evidence of lipid and DNA damage in patients with 3-hydroxy-3-methylglutaric aciduria

机译:通过3-羟基-3-甲基甲基甲基酸3-羟甲基甲基酸和3-羟基-3-甲基丁基酸患者的脂质和DNA损伤的实验证据预防DNA损伤和脂质和DNA损伤的实验证据

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摘要

3-hydroxy-3-methylglutaric aciduria (HMGA) is an inherited disorder of the leucine catabolic pathway in which occurs a deficiency of the 3-hydroxy-3-methylglutaryl-CoA lyase enzyme. Therefore, the organic acids 3-hydroxy-3-methylglutaric (HMG) and 3-methylglutaric (MGA), mainly, accumulate in tissues of affected patients. Lately, much attention has been focused on free radicals as mediators of tissue damage in human diseases, causing lipid peroxidation, protein oxidation and DNA damage. The treatment of this disease is based in a restricted protein ingest and supplementation with L-carnitine (LC), an antioxidant and detoxifying agent. In the present work, we investigated the in vitro oxidative damage to DNA induced by the accumulation of organic acids and oxidative stress parameters in vivo of patients with 3-HMG, as well as the effect of the recommended therapy. The in vitro DNA damage was analyzed by the alkaline comet assay in leukocytes incubated with HMG and MGA (1 mM, 2.5 mM and 5 mM) and co-incubated with LC (90 mu M and 150 mu M). The in vivo urinary 15-F2t-isoprostane levels and urinary oxidized guanine species were measured by ELISA kits in patient's urine before and after the treatment with LC. HMG and MGA induced a DNA damage index (DI) significantly higher than that of the control group. The DI was significantly reduced in the presence of LC. It was also verified a significant increase of oxidized guanine species and urinary isoprostane levels, biomarker of oxidative DNA damage and lipid peroxidation respectively, in patients before treatment. After the treatment and supplementation with LC, patients presented significantly lower levels of those biomarkers. Analyzing the data together, we can conclude that HMGA patients present oxidative lipid and DNA damage, which is induced by HMG and MGA, and the antioxidant therapy with LC can prevent that kind of injuries.
机译:3-羟基-3-甲基甲基酸酐酸核(HMGA)是亮氨酸分解代谢途径的遗传障碍,其出现了3-羟基-3-甲基戊齐族-COA酶酶的缺乏。因此,有机酸3-羟基-3-甲基抑制(HMG)和3-甲基抑制(MGA),主要是在受影响患者的组织中积累。最近,很多注意力都集中在自由基中作为人类疾病中组织损伤的介质,引起脂质过氧化,蛋白质氧化和DNA损伤。该疾病的治疗基于限制蛋白质摄取和补充含L-肉碱(LC),抗氧化剂和解毒剂。在目前的工作中,我们研究了通过3-HMG的患者体内积累的有机酸积累和氧化应激参数的DNA对DNA的体外氧化损伤以及推荐治疗的效果。通过与HMG和MGA(1mM,2.5mm和5mm)温育的白细胞中的碱彗星测定分析体外DNA损伤,并与LC(90μm和150μm)共孵育。在用LC处理之前和之后,通过ELISA试剂盒测量体内尿15-F2T-异前烷水平和尿氧化鸟嘌呤物种。 HMG和MGA诱导DNA损伤指数(DI)明显高于对照组。在LC存在下,DI显着降低。在治疗前,还验证了氧化鸟嘌呤种类和尿异前烷烃水平,氧化DNA损伤和脂质过氧化的生物标志物。治疗和补充LC后,患者呈现明显较低的那些生物标志物。将数据分析在一起,我们可以得出结论,HMGA患者呈现氧化脂质和DNA损伤,其由HMG和MGA诱导,并用LC抗氧化治疗可以防止这种伤害。

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