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Attention-deficit hyperactivity disorder (ADHD) and glial integrity: S100B, cytokines and kynurenine metabolism - effects of medication

机译:注意缺陷多动障碍(ADHD)和神经胶质完整性:S100B,细胞因子和犬尿氨酸代谢-药物作用

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Background Children with attention-deficit/hyperactivity disorder (ADHD) show a marked temporal variability in their display of symptoms and neuropsychological performance. This could be explained in terms of an impaired glial supply of energy to support neuronal activity. Method We pursued one test of the idea with measures of a neurotrophin reflecting glial integrity (S100B) and the influences of 8 cytokines on the metabolism of amino-acids, and of tryptophan/kynurenine to neuroprotective or potentially toxic products that could modulate glial function. Serum samples from 21 medication-na?ve children with ADHD, 21 typically-developing controls, 14 medicated children with ADHD and 7 healthy siblings were analysed in this preliminary exploration of group differences and associations. Results There were no marked group differences in levels of S100B, no major imbalance in the ratios of pro- to anti-inflammatory interleukins nor in the metabolism of kynurenine to toxic metabolites in ADHD. However, four trends are described that may be worthy of closer examination in a more extensive study. First, S100B levels tended to be lower in ADHD children that did not show oppositional/conduct problems. Second, in medicated children raised interleukin levels showed a trend to normalisation. Third, while across all children the sensitivity to allergy reflected increased levels of IL-16 and IL-10, the latter showed a significant inverse relationship to measures of S100B in the ADHD group. Fourthly, against expectations healthy controls tended to show higher levels of toxic 3-hydroxykynurenine (3 HK) than those with ADHD. Conclusions Thus, there were no clear signs (S100B) that the glial functions were compromised in ADHD. However, other markers of glial function require examination. Nonetheless there is preliminary evidence that a minor imbalance of the immunological system was improved on medication. Finally, if lower levels of the potentially toxic 3 HK in ADHD children were confirmed this could reflect a reduction of normal pruning processes in the brain that would be consistent with delayed maturation (supported here by associations with amino-acid metabolism) and a reduced metabolic source of energy.
机译:背景患有注意力缺陷/多动症(ADHD)的儿童在症状和神经心理表现方面表现出明显的时间变异性。这可以用神经胶质能量供应受损以支持神经元活动来解释。方法我们采用一种能反映神经胶质完整性的神经营养蛋白(S100B)以及8种细胞因子对氨基酸代谢以及色氨酸/犬尿氨酸对神经调节性或可能调节神经胶质功能的潜在毒性产物的影响进行了一项试验。在对群体差异和关联的初步探索中,分析了21名未接受过药物治疗的多动症儿童,21名通常正在发展的对照,14名有药物治疗的多动症儿童和7名健康兄弟姐妹的血清样本。结果ADHD中S100B的水平没有显着的组间差异,促炎性和抗炎性白介素的比例也没有显着失衡,犬尿氨酸与有毒代谢产物的代谢也无明显差异。但是,描述了四个趋势,可能需要在更广泛的研究中进行仔细研究。首先,在没有显示对立/行为问题的ADHD儿童中,S100B水平往往较低。其次,在含药儿童中,白介素水平升高显示出正常化趋势。第三,虽然在所有儿童中对过敏的敏感性反映出IL-16和IL-10水平升高,但后者与ADHD组中S100B的测量值呈显着反比关系。第四,出乎意料的是,健康对照者的毒性3-羟基犬尿氨酸(3 HK)水平往往高于ADHD。结论因此,没有明显的迹象(S100B)表明ADHD中神经胶质功能受到损害。但是,其他神经胶质功能标志物需要检查。尽管如此,有初步证据表明药物治疗可以改善免疫系统的轻微失衡。最后,如果证实多动症儿童中潜在的有毒3 HK水平较低,则可能反映出正常的大脑修剪过程减少,这与延迟成熟(此处与氨基酸代谢相关)提供了支持,并且代谢减少能量之源。

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