Plasma phthalate and bisphenol a levels and oxidant-antioxidant status in autistic children

被引:48
作者
Kondolot, Meda [1 ]
Ozmert, Elif N. [2 ]
Asci, Ali [3 ]
Erkekoglu, Pinar [3 ]
Oztop, Didem B. [4 ]
Gumus, Hakan [5 ]
Kocer-Gumusel, Belma [3 ]
Yurdakok, Kadriye [2 ]
机构
[1] Erciyes Univ, Fac Med, Dept Pediat, Social Pediat Unit, TR-38039 Kayseri, Turkey
[2] Hacettepe Univ, Fac Med, Dept Pediat, Social Pediat Unit,Dev Pediat Unit, TR-06100 Ankara, Turkey
[3] Hacettepe Univ, Fac Pharm, Dept Toxicol, TR-06100 Ankara, Turkey
[4] Erciyes Univ, Fac Med, Dept Child Psychiat, TR-38039 Kayseri, Turkey
[5] Erciyes Univ, Fac Med, Dept Pediat, Div Pediat Neurol, TR-38039 Kayseri, Turkey
关键词
Autism; Bisphenol A; Phthalate; Endocrine disruptors; Antioxidant system; INCREASED LIPID-PEROXIDATION; SPECTRUM DISORDERS; OXIDATIVE STRESS; GLUTATHIONE-PEROXIDASE; GESTATIONAL EXPOSURE; CHILDHOOD BEHAVIOR; PRENATAL EXPOSURE; ENZYMES; SERUM; GENE;
D O I
10.1016/j.etap.2016.03.006
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Phthalates and bisphenol A (BPA) are endocrine disruting chemicals (EDCs) that are suggested to exert neurotoxic effects. This study aimed to determine plasma phthalates and BPA levels along with oxidant/antioxidant status in autistic children [n = 51; including 12 children were diagnosed with "Pervasive Developmental Disorder-Not Otherwise Specified (PDD-NOS)]. Plasma levels of BPA, di (2-ethylhexyl)-phthalate (DEHP) and its main metabolite mono (2-ethylhexyl)-phthalate (MEHP); thiobarbituric acid reactive substance (TBARS) and carbonyl groups; erythrocyte glutathione peroxidase (GPx1), thioredoxin reductase (TrxR), catalase (CAT), superoxide dismutase (SOD) and glutathione reductase (GR) activities and glutathione (GSH) and selenium levels were measured. Plasma BPA levels of children with PDD-NOS were significantly higher than both classic autistic children and controls (n=50). Carbonyl, selenium concentrations and GPx1, SOD and GR activities were higher (p < 0.05); CAT activity was markedly lower in study group. BPA exposure might be associated with PDD-NOS. Intracellular imbalance between oxidant and antioxidant status might facilitate its neurotoxicity. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:149 / 158
页数:10
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