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Enzymology of Pyrimidine Metabolism and Neurodegeneration

胞苷 尿苷 生物化学 嘧啶代谢 核苷酸回收 嘧啶 磷脂酰乙醇胺 化学 磷脂酰胆碱 生物 尿苷三磷酸 核苷酸 磷脂 嘌呤 核糖核酸 基因
作者
Silvia Vincenzetti,Valeria Polzonetti,Daniela Micozzi,Stefania Pucciarelli
出处
期刊:Current Medicinal Chemistry [Bentham Science]
卷期号:23 (14): 1408-1431 被引量:37
标识
DOI:10.2174/0929867323666160411125803
摘要

It is well known that disorders of pyrimidine pathways may lead to neurological, hematological, immunological diseases, renal impairments, and association with malignancies. Nucleotide homeostasis depends on the three stages of pyrimidine metabolism: de novo synthesis, catabolism and recycling of these metabolites. Cytidine and uridine, in addition to be used as substrates for pyrimidine nucleotide salvaging, also act as the precursors of cytidine triphosphate used in the biosynthetic pathway of both brain's phosphatidylcholine and phosphatidylethanolamine via the Kennedy cycle. The synthesis in the brain of phosphatidylcholine and other membrane phosphatides can utilize, in addition to glucose, three compounds present in the blood stream: choline, uridine, and a polyunsaturated fatty acids like docosahexaenoic acid. Some authors, using rat models, found that oral administration of two phospholipid precursors such as uridine and omega-3 fatty acids, along with choline from the diet, can increase the amount of synaptic membrane generated by surviving striatal neurons in rats with induced Parkinson's disease. Other authors found that in hypertensive rat fed with uridine and choline, cognitive deficit resulted improved. Uridine has also been recently considered as a neuroactive molecule, because of its involvement in important neurological functions by improving memory, sleep disorders, anti-epileptic effects, as well as neuronal plasticity. Cytidine and uridine are uptaken by the brain via specific receptors and successively salvaged to the corresponding nucleotides. The present review is devoted to the enzymology of pyrimidine pathways whose importance has attracted the attention of several researchers investigating on the mechanisms underlying the physiopathology of brain. Keywords: Pyrimidine salvage, "de novo" pyrimidine, pyrimidine metabolism enzymes, pyrimidine homeostasis, nucleoside transport, brain phospholipids biosynthesis, neurological disorders.
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