Brosh S, Boer P, Sperling O, Zoref-Shani E
Felsenstein Medical Research Center, Rabin Medical Center, Petah-Tikva, Israel.
J Mol Neurosci. 2000 Feb-Apr;14(1-2):87-91. doi: 10.1385/JMN:14:1-2:087.
Hypoxanthine-guanine phosphoribosyltransferase (EC 2.4.2.8.; HPRT) catalyzes the salvage synthesis of inosine-5'-monophosphate (IMP) and guanosine-5'-monophosphate (GMP) from the purine bases hypoxanthine and guanine, respectively. Complete deficiency of HPRT activity is associated with the Lesch-Nyhan syndrome (LNS), characterized by excessive purine production and severe neurological manifestations. The etiology of the metabolic consequences of HPRT deficiency is clarified, but that of the neurological manifestations is not yet understood. HPRT-deficient mice represent an experimental animal model of LNS. In search for a possible metabolic abnormality in LNS brains, connecting the neurological deficit to HPRT deficiency, the purine and pyrimidine nucleotide content of cultured neurons, prepared from HPRT-deficient transgenic mice, was now determined. The HPRT-deficient neuronal cultures exhibited a significantly elevated content of the pyrimidine nucleotides UTP (1.33-fold the normal level, p = 0.0002) and CTP (1.28-fold the normal level, p = 0.02), but normal content of the purine nucleotides ATP and GTP. This abnormality in neuronal pyrimidine nucleotide content may be associated with the pathophysiology of the neurological deficit in LNS.
次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶(EC 2.4.2.8.;HPRT)分别催化由嘌呤碱次黄嘌呤和鸟嘌呤补救合成5'-肌苷酸(IMP)和5'-鸟苷酸(GMP)。HPRT活性完全缺乏与莱施 - 奈恩综合征(LNS)相关,其特征是嘌呤产生过多和严重的神经学表现。HPRT缺乏的代谢后果的病因已明确,但神经学表现的病因尚不清楚。HPRT缺陷小鼠代表LNS的实验动物模型。为了寻找LNS大脑中可能存在的代谢异常,将神经功能缺陷与HPRT缺乏联系起来,现在测定了从HPRT缺陷转基因小鼠制备的培养神经元中的嘌呤和嘧啶核苷酸含量。HPRT缺陷的神经元培养物中嘧啶核苷酸UTP(为正常水平的1.33倍,p = 0.0002)和CTP(为正常水平的1.28倍,p = 0.02)含量显著升高,但嘌呤核苷酸ATP和GTP含量正常。神经元嘧啶核苷酸含量的这种异常可能与LNS神经功能缺陷的病理生理学有关。