摘要
众所周知,嘧啶途径的失调可导致神经系统,血液,免疫疾病,肾损伤,且关联恶性肿瘤。核苷酸稳态取决于嘧啶代谢的三个阶段:de novo 合成,分解代谢和这些代谢物的回收。 胞苷和尿苷,除了用作嘧啶核苷酸打捞基板,还充当三磷酸胞苷通过肯尼迪周期用于大脑磷脂酰胆碱和磷脂酰乙醇胺的合成途径中使用的前体。脑内磷脂酰胆碱和其它膜磷脂的合成可以利用,除了葡萄糖的,存在于血液中的三种化合物:胆碱,尿苷,和多不饱和脂肪酸,如十二碳六烯酸。 一些作者,使用大鼠模型,发现有两个磷脂前体如尿苷和ω-3脂肪酸,与来源于饮食的胆碱,可以使感染诱发性帕金森病大鼠纹状体神经元存活而增加突触磷脂膜的量。其他作者发现,用尿苷和胆碱喂高血压大鼠,认知缺陷得到改善。尿苷最近也被视为神经活性分子,因为其通过改善记忆,睡眠障碍,抗癫痫作用,以及神经元可塑性而参与重要的神经功能。胞苷和尿苷是由大脑通过特异性受体摄取和相应的核苷酸打捞到的。本次综述关于重要性已引起一些研究人员研究大脑的基本病理生理机制的嘧啶途径酶学。
关键词: 嘧啶打捞,“de novo”嘧啶,嘧啶代谢酶,嘧啶动态平衡,核苷转运,脑磷脂的合成,神经系统疾病。
Current Medicinal Chemistry
Title:Enzymology of Pyrimidine Metabolism and Neurodegeneration
Volume: 23 Issue: 14
Author(s): Silvia Vincenzetti, Valeria Polzonetti, Daniela Micozzi, Stefania Pucciarelli
Affiliation:
关键词: 嘧啶打捞,“de novo”嘧啶,嘧啶代谢酶,嘧啶动态平衡,核苷转运,脑磷脂的合成,神经系统疾病。
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.
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Cite this article as:
Silvia Vincenzetti, Valeria Polzonetti, Daniela Micozzi, Stefania Pucciarelli , Enzymology of Pyrimidine Metabolism and Neurodegeneration, Current Medicinal Chemistry 2016; 23 (14) . https://dx.doi.org/10.2174/0929867323666160411125803
DOI https://dx.doi.org/10.2174/0929867323666160411125803 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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