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L-2-羟基戊二酸尿症患者氧化应激的实验证据以及左旋肉碱可减轻由D-2-羟基戊二酸和L-2-羟基戊二酸引起的体外DNA损伤。

Experimental evidence of oxidative stress in patients with l-2-hydroxyglutaric aciduria and that l-carnitine attenuates in vitro DNA damage caused by d-2-hydroxyglutaric and l-2-hydroxyglutaric acids.

作者信息

Rodrigues Daiane Grigolo Bardemaker, de Moura Coelho Daniella, Sitta Ângela, Jacques Carlos Eduardo Diaz, Hauschild Tatiane, Manfredini Vanusa, Bakkali Abdellatif, Struys Eduard A, Jakobs Cornelis, Wajner Moacir, Vargas Carmen Regla

机构信息

Programa de Pós-Graduação em Ciências Farmacêuticas, Faculdade de Farmácia, UFRGS, Av. Ipiranga, 2752, CEP 90610-000 Porto Alegre, RS, Brazil; Serviço de Genética Médica, HCPA, R. Ramiro Barcelos, 2350, CEP 90035-003 Porto Alegre, RS, Brazil.

Serviço de Genética Médica, HCPA, R. Ramiro Barcelos, 2350, CEP 90035-003 Porto Alegre, RS, Brazil.

出版信息

Toxicol In Vitro. 2017 Aug;42:47-53. doi: 10.1016/j.tiv.2017.04.006. Epub 2017 Apr 7.

Abstract

d-2-hydroxyglutaric (D-2-HGA) and l-2-hydroxyglutaric (L-2-HGA) acidurias are rare neurometabolic disorders biochemically characterized by increased levels of d-2-hydroxyglutaric acid (D-2-HG) and l-2-hydroxyglutaric acid (L-2-HG) respectively, in biological fluids and tissues. These diseases are caused by mutations in the specific enzymes involved in the metabolic pathways of these organic acids. In the present work, we first investigated whether D-2-HG and L-2-HGA could provoke DNA oxidative damage in blood leukocytes and whether l-carnitine (LC) could prevent the in vitro DNA damage induced by these organic acids. It was verified that 50μM of D-2-HG and 30μM of L-2-HG significantly induced DNA damage that was prevented by 30 and 150μM of LC. We also evaluated oxidative stress parameters in urine of L-2-HGA patients and observed a significant increase of oxidized guanine species and di-tyrosine, biomarkers of oxidative DNA and protein damage, respectively. In contrast, no significant changes of urinary isoprostanes and reactive nitrogen species levels were observed in these patients. Taken together, our data indicate the involvement of oxidative damage, especially on DNA, in patients affected by these diseases and the protective effect of LC.

摘要

D-2-羟基戊二酸(D-2-HGA)和L-2-羟基戊二酸(L-2-HGA)酸性尿症是罕见的神经代谢紊乱疾病,其生化特征分别是生物体液和组织中D-2-羟基戊二酸(D-2-HG)和L-2-羟基戊二酸(L-2-HG)水平升高。这些疾病是由这些有机酸代谢途径中特定酶的突变引起的。在本研究中,我们首先调查了D-2-HG和L-2-HGA是否会引发血液白细胞中的DNA氧化损伤,以及左旋肉碱(LC)是否能预防这些有机酸诱导的体外DNA损伤。结果证实,50μM的D-2-HG和30μM的L-2-HG显著诱导了DNA损伤,而30μM和150μM的LC可预防这种损伤。我们还评估了L-2-HGA患者尿液中的氧化应激参数,观察到氧化鸟嘌呤种类和二酪氨酸分别显著增加,它们分别是氧化DNA和蛋白质损伤的生物标志物。相比之下,在这些患者中未观察到尿中异前列腺素和活性氮物质水平的显著变化。综上所述,我们的数据表明氧化损伤,尤其是对DNA的氧化损伤,在受这些疾病影响的患者中存在,以及LC的保护作用。

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