Molecular Physiology of the Synapse Laboratory, Biomedical Research Institute Sant Pau (IIB Sant Pau), C/Sant Antoni M. Claret, 167, 08025, Barcelona, Spain.
Universitat Autònoma de Barcelona, Bellaterra, Cerdanyola del Vallès, Spain.
J Inherit Metab Dis. 2018 Nov;41(6):1093-1101. doi: 10.1007/s10545-018-0240-x. Epub 2018 Aug 21.
Neurotransmitter diseases are a well-defined group of metabolic conditions caused, in most instances, by genes specifically expressed in the presynaptic button. Better understanding of presynaptic molecular physiology, both in normal and pathological conditions, should help develop therapeutical strategies. The clinical relevance of the presynapse in inherited metabolic disorders is in glaring contrast with that of the postsynaptic component, which so far does not seem to play a relevant role in these disorders. This is somewhat surprising, as postsynaptic proteins are known to be involved in many nervous system diseases, particularly in neurodevelopmental and psychiatric disorders. The goal of this article is to explore if defects in the sophisticated postsynaptic machinery could also have a role in neurometabolic disorders.
神经递质疾病是一组明确的代谢性疾病,大多数情况下是由特定表达于突触前囊泡的基因引起的。更好地了解突触前分子生理学,无论是在正常还是病理条件下,都应该有助于开发治疗策略。在遗传性代谢紊乱中,突触前在临床相关方面与突触后成分形成鲜明对比,到目前为止,突触后成分似乎在这些紊乱中没有发挥重要作用。这有点令人惊讶,因为已知突触后蛋白参与许多神经系统疾病,特别是神经发育和精神疾病。本文的目的是探讨复杂的突触后机制缺陷是否也可能在神经代谢紊乱中起作用。