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莱施-奈恩综合征患者淋巴细胞中腺苷和多巴胺受体表达异常。

Abnormal adenosine and dopamine receptor expression in lymphocytes of Lesch-Nyhan patients.

作者信息

García M G, Puig J G, Torres R J

机构信息

Divisions of Clinical Biochemistry and Internal Medicine, La Paz University Hospital, Madrid, Spain.

出版信息

Brain Behav Immun. 2009 Nov;23(8):1125-31. doi: 10.1016/j.bbi.2009.07.006. Epub 2009 Jul 25.

Abstract

Self-injurious behavior is the most outstanding feature of Lesch-Nyhan syndrome and has recently been ascribed to an obsessive-compulsive behavior. Lesch-Nyhan syndrome results from the complete enzyme deficiency of hypoxanthine-guanine phosphoribosyl transferase (HPRT) but the link between abnormal purine metabolism and its neurological and behavioral manifestations remains largely unknown. Previous studies led us to hypothesize that adenosine and dopamine receptor expression could be altered in HPRT-deficient cells. To test this hypothesis, we examined mRNA expressions of adenosine (ADORA2A and ADORA2B) and dopamine receptors (DRD1 and DRD2 like), and dopamine transporter (DAT1) in peripheral blood lymphocytes (PBLs) from Lesch-Nyhan patients. We also examined the influence of hypoxanthine in these expressions. As compared to normal PBLs, both ADORA2A and DRD5 expression were abnormal in PBLs from Lesch-Nyhan patients. In contrast, DAT1 expression was similar to control values in HPRT deficient PBLs. These results indicate an abnormal adenosine and dopamine receptor expression in HPRT-deficient cells and suggest disrupted adenosine and dopamine neurotransmission may have a significant role in the pathogenesis of the neurological manifestations of Lesch-Nyhan syndrome.

摘要

自伤行为是莱施-奈恩综合征最突出的特征,最近被归因于一种强迫行为。莱施-奈恩综合征是由次黄嘌呤-鸟嘌呤磷酸核糖基转移酶(HPRT)完全缺乏引起的,但嘌呤代谢异常与其神经和行为表现之间的联系在很大程度上仍不清楚。先前的研究使我们推测,腺苷和多巴胺受体表达可能在HPRT缺陷细胞中发生改变。为了验证这一假设,我们检测了莱施-奈恩患者外周血淋巴细胞(PBLs)中腺苷(ADORA2A和ADORA2B)和多巴胺受体(DRD1和DRD2样)以及多巴胺转运体(DAT1)的mRNA表达。我们还检测了次黄嘌呤对这些表达的影响。与正常PBLs相比,莱施-奈恩患者PBLs中的ADORA2A和DRD5表达均异常。相比之下,HPRT缺陷的PBLs中DAT1表达与对照值相似。这些结果表明HPRT缺陷细胞中腺苷和多巴胺受体表达异常,并提示腺苷和多巴胺神经传递紊乱可能在莱施-奈恩综合征神经表现的发病机制中起重要作用。

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