Patassini Stefano, Begley Paul, Reid Suzanne J, Xu Jingshu, Church Stephanie J, Curtis Maurice, Dragunow Mike, Waldvogel Henry J, Unwin Richard D, Snell Russell G, Faull Richard L M, Cooper Garth J S
School of Biological Sciences, Faculty of Science, University of Auckland, Auckland, New Zealand; Centre for Brain Research and Department of Anatomy with Radiology, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand; Centre for Advanced Discovery and Experimental Therapeutics (CADET), Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Sciences Centre, Manchester, UK; Institute of Human Development, Faculty of Medical and Human Sciences, The University of Manchester, Manchester, UK.
Centre for Advanced Discovery and Experimental Therapeutics (CADET), Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Sciences Centre, Manchester, UK.
Biochem Biophys Res Commun. 2015;468(1-2):161-6. doi: 10.1016/j.bbrc.2015.10.140. Epub 2015 Oct 30.
Huntington's disease (HD) is a neurodegenerative disorder wherein the aetiological defect is a mutation in the Huntington's gene (HTT), which alters the structure of the huntingtin protein through the lengthening of a polyglutamine tract and initiates a cascade that ultimately leads to dementia and premature death. However, neurodegeneration typically manifests in HD only in middle age, and processes linking the causative mutation to brain disease are poorly understood. Here, our objective was to elucidate further the processes that cause neurodegeneration in HD, by measuring levels of metabolites in brain regions known to undergo varying degrees of damage. We applied gas-chromatography/mass spectrometry-based metabolomics in a case-control study of eleven brain regions in short post-mortem-delay human tissue from nine well-characterized HD patients and nine controls. Unexpectedly, a single major abnormality was evident in all eleven brain regions studied across the forebrain, midbrain and hindbrain, namely marked elevation of urea, a metabolite formed in the urea cycle by arginase-mediated cleavage of arginine. Urea cycle activity localizes primarily in the liver, where it functions to incorporate protein-derived amine-nitrogen into urea for recycling or urinary excretion. It also occurs in other cell-types, but systemic over-production of urea is not known in HD. These findings are consistent with impaired local urea regulation in brain, by up-regulation of synthesis and/or defective clearance. We hypothesize that defective brain urea metabolism could play a substantive role in the pathogenesis of neurodegeneration, perhaps via defects in osmoregulation or nitrogen metabolism. Brain urea metabolism is therefore a target for generating novel monitoring/imaging strategies and/or therapeutic interventions aimed at ameliorating the impact of HD in patients.
亨廷顿舞蹈症(HD)是一种神经退行性疾病,其病因缺陷是亨廷顿基因(HTT)发生突变,该突变通过延长聚谷氨酰胺序列改变亨廷顿蛋白的结构,并引发一系列最终导致痴呆和过早死亡的连锁反应。然而,神经退行性变在HD中通常仅在中年时才会显现,且将致病突变与脑部疾病联系起来的过程尚不清楚。在此,我们的目标是通过测量已知会受到不同程度损伤的脑区中的代谢物水平,进一步阐明HD中导致神经退行性变的过程。我们在一项病例对照研究中,对来自9名特征明确的HD患者和9名对照的死后短时间延迟的人体组织中的11个脑区应用了基于气相色谱/质谱的代谢组学技术。出乎意料的是,在前脑、中脑和后脑研究的所有11个脑区中都出现了一个单一的主要异常情况,即尿素显著升高,尿素是精氨酸酶介导的精氨酸裂解在尿素循环中形成的一种代谢物。尿素循环活动主要定位于肝脏,在肝脏中其功能是将蛋白质衍生胺氮整合到尿素中以便循环利用或经尿液排泄。它也发生在其他细胞类型中,但HD中尿素的全身过度产生情况尚不清楚。这些发现与大脑中局部尿素调节受损一致,可能是合成上调和/或清除缺陷所致。我们推测,有缺陷的脑尿素代谢可能在神经退行性变的发病机制中起重要作用,或许是通过渗透调节或氮代谢缺陷。因此,脑尿素代谢是开发旨在减轻HD对患者影响的新型监测/成像策略和/或治疗干预措施的一个靶点。