Uridine and its role in metabolic diseases, tumors, and neurodegenerative diseases

被引:17
作者
Yang, Yueyuan [1 ]
Ye, Yahong [2 ]
Deng, Yingfeng [3 ]
Gao, Ling [1 ]
机构
[1] Wuhan Univ, Renmin Hosp, Dept Endocrinol, Wuhan, Peoples R China
[2] QuanZhou Womens & Childrens Hosp, Dept Internal Med, Quanzhou, Peoples R China
[3] City Hope Natl Med Ctr, Dept Diabet & Canc Metab, Duarte, CA 91010 USA
基金
美国国家科学基金会;
关键词
uridine; metabolic diseases; circadian rhythm; diabetes; O-GlcNAc; obesity; neurodegenerative diseases; PLASMA-CONCENTRATION; SYNAPSE FORMATION; O-GLCNACYLATION; DOWN-REGULATION; PPAR-ALPHA; BRAIN; ACTIVATION; GLYCOSYLATION; DYSFUNCTION; ACID;
D O I
10.3389/fphys.2024.1360891
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Uridine is a pyrimidine nucleoside found in plasma and cerebrospinal fluid with a concentration higher than the other nucleosides. As a simple metabolite, uridine plays a pivotal role in various biological processes. In addition to nucleic acid synthesis, uridine is critical to glycogen synthesis through the formation of uridine diphosphate glucose in which promotes the production of UDP-GlcNAc in the hexosamine biosynthetic pathway and supplies UDP-GlcNAc for O-GlcNAcylation. This process can regulate protein modification and affect its function. Moreover, Uridine has an effect on body temperature and circadian rhythms, which can regulate the metabolic rate and the expression of metabolic genes. Abnormal levels of blood uridine have been found in people with diabetes and obesity, suggesting a link of uridine dysregulation and metabolic disorders. At present, the role of uridine in glucose metabolism and lipid metabolism is controversial, and the mechanism is not clear, but it shows the trend of long-term damage and short-term benefit. Therefore, maintaining uridine homeostasis is essential for maintaining basic functions and normal metabolism. This article summarizes the latest findings about the metabolic effects of uridine and the potential of uridine metabolism as therapeutic target in treatment of metabolic disorders.
引用
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页数:11
相关论文
共 81 条
[1]   INTRAVENOUS URIDINE TREATMENT ANTAGONIZES HYPOGLYCEMIA-INDUCED REDUCTION IN BRAIN SOMATOSTATIN-LIKE IMMUNOREACTIVITY [J].
AGNATI, LF ;
FUXE, K ;
ENEROTH, P ;
ZINI, I ;
HARFSTRAND, A ;
GRIMALDI, R ;
ZOLI, M .
ACTA PHYSIOLOGICA SCANDINAVICA, 1986, 126 (04) :525-531
[2]   Accumulation of sorbitol in the sciatic nerve modulates circadian properties of diabetes-induced neuropathic pain hypersensitivity in a diabetic mouse model [J].
Akamine, Takahiro ;
Kusunose, Naoki ;
Matsunaga, Naoya ;
Koyanagi, Satoru ;
Ohdo, Shigehiro .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2018, 503 (01) :181-187
[3]   HPLC reveals novel features of nucleoside and nucleobase homeostasis, nucleoside metabolism and nucleoside transport [J].
Altaweraqi, Reema A. ;
Yao, Sylvia Y. M. ;
Smith, Kyla M. ;
Cass, Carol E. ;
Young, James D. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2020, 1862 (07)
[4]   Specific O-GlcNAc modification at Ser-615 modulates eNOS function [J].
Aulak, Kulwant S. ;
Barnes, Jarrod W. ;
Tian, Liping ;
Mellor, Noel E. ;
Haque, Mohammad M. ;
Willard, Belinda ;
Li, Ling ;
Comhair, Suzy C. ;
Stuehr, Dennis J. ;
Dweik, Raed A. .
REDOX BIOLOGY, 2020, 36
[5]   Roles of O-GlcNAc in chronic diseases of aging [J].
Banerjee, Partha S. ;
Lagerloef, Olof ;
Hart, Gerald W. .
MOLECULAR ASPECTS OF MEDICINE, 2016, 51 :1-15
[6]   Effect of Chronic Treatment with Uridine on Cardiac Mitochondrial Dysfunction in the C57BL/6 Mouse Model of High-Fat Diet-Streptozotocin-Induced Diabetes [J].
Belosludtseva, Natalia, V ;
Starinets, Vlada S. ;
Mikheeva, Irina B. ;
Belosludtsev, Maxim N. ;
Dubinin, Mikhail, V ;
Mironova, Galina D. ;
Belosludtsev, Konstantin N. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (18)
[7]   A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis [J].
Bostroem, Pontus ;
Wu, Jun ;
Jedrychowski, Mark P. ;
Korde, Anisha ;
Ye, Li ;
Lo, James C. ;
Rasbach, Kyle A. ;
Bostroem, Elisabeth Almer ;
Choi, Jang Hyun ;
Long, Jonathan Z. ;
Kajimura, Shingo ;
Zingaretti, Maria Cristina ;
Vind, Birgitte F. ;
Tu, Hua ;
Cinti, Saverio ;
Hojlund, Kurt ;
Gygi, Steven P. ;
Spiegelman, Bruce M. .
NATURE, 2012, 481 (7382) :463-U72
[8]   Uridine and cytidine in the brain: Their transport and utilization [J].
Cansev, Mehmet .
BRAIN RESEARCH REVIEWS, 2006, 52 (02) :389-397
[9]   Uridine homeostatic disorder leads to DNA damage and tumorigenesis [J].
Cao, Zhe ;
Ma, Jun ;
Chen, Xinchun ;
Zhou, Boping ;
Cai, Chuan ;
Huang, Dan ;
Zhang, Xuewen ;
Cao, Deliang .
CANCER LETTERS, 2016, 372 (02) :219-225
[10]   Control of glycolytic flux in directed biosynthesis of uridine-phosphoryl compounds through the manipulation of ATP availability [J].
Chen, Yong ;
Liu, Qingguo ;
Chen, Xiaochun ;
Wu, Jinglan ;
Xie, Jingjing ;
Guo, Ting ;
Zhu, Chenjie ;
Ying, Hanjie .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2014, 98 (15) :6621-6632