Functionalities of Purines in Health and Disease
Abstract
Purines conduct several vital cellular functions as in the production of the numeric-precursors of nucleic acids, whereas excess formation of uric acid generated from purines metabolism has been expansively implicated in human disease. The physiological functions and pathogenic attributes of uric acid have been linked to the imminent presentations of cardiovascular abnormalities, diabetes and stroke. Inasmuch as the overproduction of uric acid results in gout, it is established that uric acid constitutes a potent antioxidant in the shielding of DNA from single-strand breaks due to free radicals culminating in a protective effect in neurodegenerative disorders for an extended life span. Thus, this paper describes certain contronymic effects in the functionalities of purines in health and disease.
Full Text:
PDFReferences
The George Mateeljan Foundation. What are purines and how are they related to food and health? 2016. http://www.whfoods.com/genpage.php?tname+george&abid+51.
Helmut R. The chemodiversity of purine as a constituent of natural products. Chemistry and Biodiversity, 2004; 1(3): pp. 361-401.
Elguero j., Marzin C., Katritzky A.R. & Linda P. The Tautomerism of Heterocycles. Academic Press New York. 1976: pp. 655.
Dietaryfiberfood.com. 2016. List of Foods High and Low in purine content. 2016. https://www.dietfiberfood.com/purine-and-uric-acid/purines-food-and-gout.php.
Hill D.L. & Bennett C.L. Purification and properties of 5-phosphoribosyl pyrophosphate amidotransferase from adenocarcinoma 755 cells. Biochemistry. 1969; 8: pp. 122-130.
Rowe B. & Coleman M.D., Wyngaarden J.B. Glutamine phosphoribosylphosphate amidotransferase. Catalytic and conformational heterogeneity of the pigeon liver enzyme. Biochemistry. 1970; 9: pp. 1498-1505.
Gots J.S. Purine metabolism in bacteria. V. Feedback inhibition. J Biol Chem. 1957; 228: pp. 57-66.
Brockman R.W. & Chumley S. Inhibition of Formyl. Glycinamide Eibonucleotide synthesis in neoplastic cells by purines and analogs. Biochim Biophys Acta. 1965; 95: pp. 365-379.
Walsh M. Disorders of purine and pyrimidine metabolism. Pediatrics. 2018. https://www.cancertherapyadvisor.com/pediatrics/disorders-of-purine-and-pyrimidine-metabolism/article/623080.
Fontenelle L.J. & Henderson J.F. An enzymatic basis for the inability of rythrocytes to synthesize purine ribonucleotides de novo. Biochim Biophys Acta, 1969; 177: pp. 175-176.
Bartlett G.R. Phosphorous compounds in the human erythrocyte. Biochim Biophys Acta, 1968; 156: pp. 221-230.
Lichtman M.A & Miller D.R. Erythrocyte glycolysis, 2, 3-diphosphoglycerate and adenosine triphosphate concentration in uremic subjects: relationship to extracellular phosphate concentration. J Lab Clin Med, 1970; 76: pp. 267-279.
Rapoport S., Guest G.M. & Wing M. Hypoprothrombinemis after salicylate asministration in man and rabbits. Proc Soc Exp Biol Med, 1944; 57: pp. 344-347.
Shemin D. & Rittenberg D. The life span of the human red blood cell. J Biol Chem, 166: pp. 627-636.
Barnard E.A. Ribonucleases. Ann Rev Biochem, 1946; 38: pp. 677-732.
Sorensen LB. The elimination of uric acid in man. Studied by means of C14-labeled uric acid, uricolysis. Scand J Clin Lab Invest, 1960; 12: Supl 54.
Edozien J.C., Udo U.U., Young V.R. & Schrimshaw N.S. Effects of high levels of yeast feeding on uric acid metabolism of young men. Nature, 1970; 228: pp. 180.
Pritchard J.B., Chavez-Peon F. & Berlin R.D. Purines: Supply by liver to tissues. Am J Physiol, 1970; 219: pp. 1263.
Roll P.M., Weinfeld H., Carroll E. & Brown G.B. The utilization of nucleotides by the mammal. IV. Triply labeled purine nucleotides. J Biol Chem, 1956; 220: pp. 439-454.
Murray AW. The biological significance of purine salvage. Ann Rev Biochem, 1971; 40: pp. 811-826.
Al-Khalidi U.A.S. & Chaglassian T.H. The species distribution of xanthine oxidase. Biochem J, 1965; 97: pp. 316-320.
Kelley W.N., Greene M.L., Rosenbloom F.M. et al. Hypoxanthine-guanine phosphoribosyl transferase deficiency in gout. Ann Intern Med, 1969; 70: pp. 155-206.
Orsulak P.J., Haab W., Appleton M.D. Quantitative estimation of uric acid, xanthine, and hypoxanthine in plasma using thin-layer chromatography. Anal Biochem, 1968; 23: pp. 156-162.
Jorgensen S. Breakdown of adenine and hypoxanthine nucleotides and nucleosides in human plasma. Acta Pharmacol Toxicol, 1956; 12: pp. 303-309.
Craft JA, Dean BM, Watts RWE & Westwick WJ. Studies on human erythrocyte IMP: pyrophosphate phosphoribosyltransferase. Eur J Biochem, 1970; 15: pp. 367-373.
Lowy B.A., Williams M.K. & London L.M. The utilization of purines and their ribosyl derivatives for the formation of adenosine triphosphate and guanine triphosphate in the mature rabbit erythrocyte. J Biol Chem, 1961; 236: pp. 1439-1441.
Lowy B.A., Williams M.K. & London I.M. Enzymatic deficiencies of purine nucleotide synthesis in the human erythrocyte. J Biol Chem, 1962; 237: pp. 1622-1625
Mager J., Dvilansky A., Razin et al. Turnover of purine nucleotides in human red blood cells. Israel J Med Sci, 1966; 2: pp. 297-301.
Kelley W.N., Fox I.H. & Wyngaarden J.B. Regulation of purine biosynthesis in cultured human cells. I. Effects of orotic acid. Clin Res, 1970; 18: pp. 53.
Hershko A., Razin A. & Mager J. Regulation of the synthesis of 5-phosphoribosyl-1-pyrophosphate in intact red blood cells and in cell-free preparations. Biochim Biophys Acta, 1969; 184: pp. 64-76.
Henderson J.F., Brox L.W., Kelley W.N. et al. Kinetic studies of hypoxanthine-guanine phosphoribosyltransferase. J Biol Chem, 1968; 243: pp. 2514-2522.
Bishop C. Purine metabolism in human and chicken blood in vitro. J Biol Chem, 1960; 235: pp. 3228-3232.
Wong P.C.L. Regulation of 5-phosphoribosyl-1-pyrophosphate synthesis. PhD Thesis. Flinders University South Australia. 1970, pp. 11.
Vanderheiden B.S. Human erythrocyte “ITPase”, an ITP pyrophosphohydrolase. Biochim Biophys Acta, 1970; 215: pp. 242-248
Villegas R., Xiang Y-B & Elasy T. Purine-rich foods, protein intake, and the prevalence of hyperuricaemia: The Shangai Men’s Health Study. Nutr Metab Cardiovasc Dis, 2011; 22(5): pp. 409-416.
Choi H.K., Willett W. & Curhan G. Fructose-rich beverages and risk of gout in women. JAMA. 2010; 304: pp. 2270-2278.
Clifford A., Riumallo J., Young V. et al. Effect of oral purines on serum and urinary uric acid of normal, hyperuricemic and gouty humans. J Nutr, 1978; 106: pp. 428-434.
Bardin P.R.C. Purine-rich foods: an innocent bystander of gout attacks? Ann Rheum Dis, 2012; 71: pp. 1435-1436.
Jimenez M.L., Puig J.G., Mateos A.N. et al. Purine transport through the blood brain barrier in hypoxanthine phosphoribosyl transferase deficiency. Med Clin (Barc), 1989; 92(5): pp. 167-170.
Howard W.J. Synthesis de novo of purines in slices of rat brain and liver. J Neurochem, 1970; 17: pp. 121-128.
Rosenbloom F.M., Kelley W.N., Miller J. et al. Inherited disorders of purine metabolism. JAMA, 1967; 202: pp. 175-177.
Berlin R.D. Purines: Active transport by isolated choroid plexus. Science, 1969; 163: pp. 1194-1195.
Halgren R., Niklasson A. Terent A. et al. Oxypurines in cerebrospinal fluid as indices of disturbed brain disease. Stroke, 1983; 14: pp. 382-388.
Moyer JD & Henderson JF. Salvage of circulating hypoxanthine by tissues of the mouse. Can J Biochem Cell Biol, 1983; 61: 1153-1157.
Spector R. Hypoxanthine transport through the blood-brain-barrier. Neurochem Res, 1987; 12: pp. 791-796.
Kelley W.N. & Wyngaarden J.B. Clinical syndromes associated with hypoxanthine-guanine phosphoribosyltransferase deficiency. In: The Metabolic Basis of Inherited Diseases. JB Stanbury, JB Wyngaarden, DS Frederickson, JL Goldstein and MS Brown (eds). McGraw Hill, NY, 1983; pp. 1115-1143.
Brosh S., Boer P., Kupfer B. et al. De novo synthesis of purine nucleotides in human peripheral blood leukocytes. Excessive activity of the pathway in hypoxanthine-guanine phosphoribosyltransferase deficiency. J Clin Invest. 1976; 58(2): pp. 289-297.
Becker M.A., Kim M., Husain K. & Kang T. Regulation of purine nucleotide synthesis in human B lymphoblasts with both hypoxanthine-guanine phosphoribosyltransferase deficiency and phosphoribosylpyrophosphate synthetase superactivity. J Biol Chem, 1992; 267(7): pp. 4317-4321.
Moffat B.A. & Ashihara H. Purine and pyrimidine nucleotide synthesis and metabolism. Arabidopsis Book. 2002; 1: e0018. Doi: 10.1199/tab.0018. https://www.ncbi.nlm.nih.gov/pmc3243375/.
Lane A.N. & Fan TW-M. Regulation of mammalian nucleotide metabolism and biosynthesis. Nucleic Acid Res, 2015; 43(4):2466-2485. DOI: 10.1093/nar/gkv047.
Sobotka L., Cervinkova Z. & Palicka V. Reutilization of 14C-thymidine in the liver of young and adult mice. J Hepatology. 1998; 28(3): pp. 234 Doi: 10.1016/so168.8278(98)81106-9.
Skaper S.D., O’Brien W.E. & Schafer I.A. The influence of ammonia on purine and pyrimidine nucleotide biosynthesis in rat liver and brain in vitro. Biochem J, 1978; 172(3): pp. 457-464.
Watts R.W. Some regulatory and integrative aspects of purine nucleotide biosynthesis and its control: an overview. Adv Enzyme Reg, 1983; 21: pp. 33-51.
Berman P.A., Black D.A. & Harley E.H. Oxypurine cycle in human erythrocytes regulated by pH, inorganic phosphate, and oxygen. J Clin Invest. 82(3): pp. 980-986.
Schendel F.J., Cheng Y.S. & Stubbe J. Characterization and chemical properties of phosphoribosylamine, an unstable intermediate in the de Novopurine biosynthetic pathway. Biochemistry, 1988; 27(7): pp. 2614-2623.
Nierlich D.P. & Magasanik B. Phosphoribosylglycinamide synthetase of Aerobacter aerogenes. J Biol Chem, 1965; 240: pp. 358-365.
Jimenez M.L., Puig J.G., Mateos F.A. et al. Hypoxanthine and xanthine transport through the blood-brain-barrier in hypoxanthine phosphoribosyltransferase (HPRT) deficiency. Adv Exp Med Biol, 1989; 253A: pp. 173-179.
Torres R.J., Prior C. & Puig J.G. Efficacy and safety of allopurinol in patients with hypoxanthine guanine phosphoribosyltransferase deficiency. Metabolism. 2007; 56(9): pp. 1179-1186.
Burnstock G. & Pelleg A. Cardiac purinergic signaling in health and disease. Purinergic Signal. 2015; 11(1): pp. 1-46.
So A. &Thorens B. Uric acid transport and disease. J Clin Invest. 2010; 120(6): pp. 1791-1799.
Maluolo J., Oppedisano F., Gratteri S. et al. Regulation of uric acid metabolism and excretion. Int J Cardiology. 2016; 213: pp. 8-14.
Lesch M. & Nyhan W.L. A familial disorder of uric acid metabolism and central nervous system function. Am J Med. 1964; 36: pp. 561-570.
Jinnah H.A. & Friedman T. Lesch-Nyhan disease and its variants. 2016; Doi: 10.1036/ommbid.135.
Garcia-Pavia P. Toress R.J., Rivero M. et al. Phosphoribosylpyrophosphate synthetase overactivity as a cause of uric acid overproduction in a young woman. Arthritis & Rheumatology, 2003; 48(7): pp. 2036-2041.
Tasca C.I., Lanznaster D., Oliveira I.K. & Ciruela F. Neuromodulatory effects of guanine-based purines in health and disease. Frontiers in Cellular Neuroscience. 2018; 23. https://doi.org/10.3389/fncel.2018.00376.
Fumagalli M., Lecca D., Abbracchio M.P. & Ceruti S. Pathophysiological role of purines and pyrimidines in neurodevelopment. Unveiling new pharmacological approaches to congenital brain diseases. Front. Pharmacol. 2017. https://doi.org/10.3389/fphar.2017.00941.
Maria-Gilt M., Camici M., Allegrini S., Pesi R., Petrotto E. & Tozzi M.G. Emerging role of purine metabolizing enzymes in brain functions and tumors. Int. J. Mol. Sci. 2018, 19(1): pp. 3598.
Refbacks
- There are currently no refbacks.