Inborn Errors of Metabolism, Clinical Chemistry Laboratory, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland.
J Neurochem. 2010 Oct;115(2):297-313. doi: 10.1111/j.1471-4159.2010.06935.x. Epub 2010 Aug 25.
Apart of its well known function of 'energetic buffer' through the creatine/phosphocreatine/creatine kinase system allowing the regeneration of ATP, creatine has been recently suggested as a potential neuromodulator of even true neurotransmitter. Moreover, the recent discovery of primary creatine deficiency syndromes, due to deficiencies in L-arginine : glycine amidinotransferase or guanidinoacetate methyltransferase (the two enzymes allowing creatine synthesis) or in the creatine transporter, has shed new light on creatine synthesis, metabolism and transport, in particular in CNS which appears as the main tissue affected by these creatine deficiencies. Recent data suggest that creatine can cross blood-brain barrier but only with a poor efficiency, and that the brain must ensure parts of its needs in creatine by its own endogenous synthesis. Finally, the recent years have demonstrated the interest to use creatine as a neuroprotective agent in a growing number of neurodegenerative diseases, including Parkinson's and Huntington's diseases. This article aims at reviewing the latest data on creatine metabolism and transport in the brain, in relation to creatine deficiencies and to the potential use of creatine as neuroprotective molecule. Emphasis is also given to the importance of creatine for cerebral function.
除了通过肌酸/磷酸肌酸/肌酸激酶系统作为众所周知的“能量缓冲剂”的功能,使 ATP 得以再生之外,肌酸最近还被认为是一种潜在的神经调节剂,甚至是真正的神经递质。此外,由于 L-精氨酸:甘氨酸酰胺转移酶或胍乙酸甲基转移酶(允许肌酸合成的两种酶)或肌酸转运蛋白的缺乏,导致原发性肌酸缺乏症的最近发现,为肌酸的合成、代谢和转运提供了新的认识,特别是在中枢神经系统,因为中枢神经系统似乎是这些肌酸缺乏症的主要受影响组织。最近的数据表明,肌酸可以穿过血脑屏障,但效率很低,大脑必须通过自身的内源性合成来确保其自身对肌酸的部分需求。最后,近年来的研究表明,在越来越多的神经退行性疾病中,肌酸作为一种神经保护剂具有很大的应用潜力,包括帕金森病和亨廷顿病。本文旨在综述大脑中肌酸代谢和转运的最新数据,以及与肌酸缺乏症和肌酸作为神经保护分子的潜在用途有关的最新数据。本文还强调了肌酸对大脑功能的重要性。