ISSN 2415-3060 (print), ISSN 2522-4972 (online)
  • 46 of 60
Up
УЖМБС 2019, 4(6): 309–315
https://doi.org/10.26693/jmbs04.06.309
Biology

Anti–Glycation Aging Prevention Strategies

Boiarska Z.
Abstract

The article provides overview data on modern theories of aging. Aging is a complex process that occurs under the influence of endogenous and exogenous factors. Among the external factors of skin aging, ultraviolet radiation, xenobiotic effects and poor nutrition have the greatest influence. Particular attention is paid to the consideration of modern biomarkers of skin aging, which allows establishing the type of skin aging, the leading mechanisms of skin aging, and to select an adequate strategy for the prevention of skin aging. Today, biomarkers of aging, such as reactive oxygen species, mitochondrial dysfunction, decreased activity of antioxidant defense mechanisms (due to free radical processes), DNA damage (due to ultraviolet radiation), telomere shortening, and decreased telomerase activity (due to due to chronic aging) and the possibility of increasing their activity. Particular attention is paid to glycation processes, its mechanisms and the role of glycation end products in the development of oxidative and glycation stress. Two directions are distinguished: the search for substances that inhibit the formation of end glycation products, and the search for substances that disrupt the structure of final glycation products. The characteristics of substances are given, they are actively studied in our time and have anti–glycation effects (aminoguanidine, thiamine, pyridoximine, metmorphine, carnosine, α–lipoic acid, plant extracts). The purpose of this work was to determine the main views on the mechanisms of aging and analysis of substances that reduce the glycation of proteins according to literature. Сonclusion. The article proved that, based on the theory of glycation, as one of the modern theories of skin aging, the amount of final glycation products accumulates in the skin, which leads to the development of glycation and oxidative stress and irreversible changes in the structure of collagen and other skin proteins. However, the use of substances that reduce glycation and have antioxidant properties is an important component of programs for the prevention of skin aging and the correction of visible signs of skin aging, and determines the relevance of this review article.

Keywords: aging, glycation, glycic stress, oxidative stress, antiglycants

Full text: PDF (Ukr) 216K

References
  1. Getoff N Anti–aging and aging factors in life. The role of free radicals. Radiation Physics and Chemistry. 2007; 76(10): 1577–86.
  2. Farage MA, Miller KW, Elsner P, Maibach HI. Intrinsic and extrinsic factors in skin ageing: a review. International Journal of Cosmetic Science. 2008; 30(2): 87–95. https://www.ncbi.nlm.nih.gov/pubmed/18377617. https://doi.org/10.1111/j.1468–2494.2007.00415.x
  3. Vierkötter A, Krutmann J. Environmental influences on skin aging and ethnic–specific manifestations. Dermato–Endocrinology. 2012; 4(3): 227–31. https://www.ncbi.nlm.nih.gov/pubmed/23467702. https://www.ncbi.nlm.nih.gov/pmc/articles/3583881. https://doi.org/10.4161/derm.19858
  4. Fischer GJ, Wang ZQ, Datta SC, Varani J, Kang S, Voorhees JJ. Pathophysiology of premature skin aging induced by ultraviolet light. New England Journal of Medicine. 1997; 337(20): 1419–28. https://www.ncbi.nlm.nih.gov/pubmed/9358139. https://doi.org/10.1056/NEJM199711133372003
  5. Flament F, Bazin R, Laquieze S, Rubert V, Simonpietri E, Piot B. Effect of the sun on visible clinical signs of aging in Caucasian skin. Clinical, Cosmetic and Investigational Dermatology. 2013; 6: 221–32. https://www.ncbi.nlm.nih.gov/pubmed/24101874. https://www.ncbi.nlm.nih.gov/pmc/articles/3790843. https://doi.org/10.2147/CCID.S44686
  6. Gkogkolou P, Bohm M. Advanced glycation end products. Key players in skin aging? Dermatoendocrinol. 2012; 4(3): 259–70. https://www.ncbi.nlm.nih.gov/pubmed/23467327. https://www.ncbi.nlm.nih.gov/pmc/articles/3583887. https://doi.org/10.4161/derm.22028
  7. Grebneva EA. Priroda i vozmozhnyie mehanizmyi obrazovaniya potentsialnyih mutatsiy, voznikayuschih pri poyavlenii timinovyih dimerov posle oblucheniya dvuhtsepochechnoy DNK ultrafioletovyim svetom. Biopolimeri i klitina. 2002; 18 (3): 205–18. [Russian]
  8. Rattan SI. Theories of biological aging: genes, proteins, and free radicals. Free Radic Res. 2006; 40(12): 1230–8. https://www.ncbi.nlm.nih.gov/pubmed/17090411. https://doi.org/10.1080/10715760600911303
  9. Lindahl T. Instability and decay of the primary structure of DNA. Nature. 1993; 362(6422): 709–15. https://www.ncbi.nlm.nih.gov/pubmed/8469282. https://doi.org/10.1038/362709a0
  10. Moldogazieva NT, Mokhosoev IM, Melnikova TI, Porozov YuB, Terentyev AA. Oxidative stress and advanced lipoxidation and glycation products (ALEs and AGE) in the field of aging and age–related diseases. Oxid Med Cell Longev. 2019 Aug 14; 2019: 3085756. https://www.ncbi.nlm.nih.gov/pubmed/31485289. https://www.ncbi.nlm.nih.gov/pmc/articles/6710759. https://doi.org/10.1155/2019/3085756
  11. Park DC, Yeo SG. Aging. Korean Journal of Audiology 2013; 17(2): 39–44. https://www.ncbi.nlm.nih.gov/pubmed/24653904. https://www.ncbi.nlm.nih.gov/pmc/articles/3936540. https://doi.org/10.7874/kja.2013.17.2.39
  12. Vina J, Borras C, Abdelaziz KM, Garcia–Valles R, Gomez–Cabrera MC. The free radical theory of aging revisited: The cell signaling disruption theory of aging. Antioxid Redox Signal. 2013; 19(8): 779–87. https://www.ncbi.nlm.nih.gov/pubmed/23841595. https://www.ncbi.nlm.nih.gov/pmc/articles/3749699. https://doi.org/10.1089/ars.2012.5111
  13. Gladyshev VN. The free radical theory of aging is dead. Long live the damage theory! Antioxid Redox Signal. 2014; 20(4): 727–31. https://www.ncbi.nlm.nih.gov/pubmed/24159899. https://www.ncbi.nlm.nih.gov/pmc/articles/3901353. https://doi.org/10.1089/ars.2013.5228
  14. Harman D. The biologic clock: The mitochondria? J Am Geriatr Soc. 1972; 20(4): 145–7. https://www.ncbi.nlm.nih.gov/pubmed/5016631. https://doi.org/10.1111/j.1532-5415.1972.tb00787.x
  15. Samper E, Nicholls DG, Melov S. Mitochondrial oxidative stress causes chromosomal instability of mouse embryonic fibroblasts. Aging Cell. 2003; 2(5): 277–85. https://www.ncbi.nlm.nih.gov/pubmed/14570235. https://doi.org/10.1046/j.1474-9728.2003.00062.x
  16. Lee HC, Chang CM, Chi CW. Somatic mutations of mitochondrial DNA in aging and cancer progression. Ageing Res Rev. 2010; 9: 47–58. https://www.ncbi.nlm.nih.gov/pubmed/20816876. https://doi.org/10.1016/j.arr.2010.08.009
  17. Victor VM, Rocha M, Herance R, Hernandez–Mijares A. Oxidative stress and mitochondrial dysfunction in type 2 diabetes. Curr Pharm Des. 2011; 17(36): 3947–58. https://www.ncbi.nlm.nih.gov/pubmed/22188447. https://doi.org/10.2174/138161211798764915
  18. Ramamoorthy M, Sykora P, Scheibye–Knudsen M, Dunn C, Kasmer C, Zhang Y, et al. Sporadic Alzheimer disease fibroblasts display an oxidative stress phenotype. Free Radic Biol Med. 2012; 53(6): 1371–80. https://www.ncbi.nlm.nih.gov/pubmed/22885031. https://www.ncbi.nlm.nih.gov/pmc/articles/4617209. https://doi.org/10.1016/j.freeradbiomed.2012.07.018
  19. Lagouge M, Larsson NG. The role of mitochondrial DNA mutations and free radicals in disease and ageing. Intern Med. 2013; 273(6): 529–43. https://www.ncbi.nlm.nih.gov/pubmed/23432181. https://www.ncbi.nlm.nih.gov/pmc/articles/3675642. https://doi.org/10.1111/joim.12055
  20. Marzetti E, Csiszar A, Dutta D, Balagopal G, Calvani R, Leeuwenburgh C. Role of mitochondrial dysfunction and altered autophagy in cardiovascular aging and disease: From mechanisms to therapeutics. Am J Physiol Heart Circ Physiol. 2013; 305(4): 459–76. https://www.ncbi.nlm.nih.gov/pubmed/23748424. https://www.ncbi.nlm.nih.gov/pmc/articles/3891249. https://doi.org/10.1152/ajpheart.00936.2012
  21. Maillard LC. Reaction generale des acides amines sur le sucres: ses consequences biologiques. CR Acad Sci. 1912; 154: 66–8.
  22. Cho S–J, Roman G, Yeboah F, Konishi Y. The road to advanced glycation end. Curr med chem. 2007; 14(15): 1653–71. https://www.ncbi.nlm.nih.gov/pubmed/17584071. https://doi.org/10.2174/092986707780830989
  23. Mossine VV, Mawhinney TP. 1–Amino–1–deoxy–D–fructose (“fructosamine”) and its derivatives. Adv Carbohydr Chem Biochem. 2010; 64: 291–402. https://www.ncbi.nlm.nih.gov/pubmed/31417772. https://www.ncbi.nlm.nih.gov/pmc/articles/6690447. https://doi.org/10.1107/S2056989019009253
  24. Ahmed N. Advanced glycation end products–role in pathology of diabetic. Diabetes Res Clin Pract. 2005; 67(1): 3–21. https://www.ncbi.nlm.nih.gov/pubmed/15620429. https://doi.org/10.1016/j.diabres.2004.09.004
  25. Abdallah HM, Zakaria EM, El–Halawany AM, Mohamed GA, Safo MK, El–Bassossy HM. Psiadia punctulata major flavonoids alleviate exaggerated vasoconstriction produced by advanced glycation end products. PLoS One. 2019 Sep 6; 14(9): e0222101. https://www.ncbi.nlm.nih.gov/pubmed/31491007. https://doi.org/10.1371/journal.pone.0222101
  26. Rasool M, Malik A, Butt TT, Ashraf MAB, Rasool R, Zahid A, et al. Implications of advanced oxidation protein products (AOPPs), advanced glycation end products (AGEs) and other biomarkers in the development of cardiovascular diseases. Saudi J Biol Sci. 2019 Feb; 26(2): 334–9.
  27. Lozinska LM, Cemchishin GM. Biologichni aspekti neenzimatichnogo glikozilyuvannya. Ukr biohim zhurn. 2012; 84(5): 16–37.
  28. Hou FF, Boyce J, Chertow GM, Kay J, Owen WF Jr. Aminoguanidine inhibits advanced glycation end products formation on beta2–microglobulin. J Am Soc Nephrol. 1998; 9(2): 277–83. https://www.ncbi.nlm.nih.gov/pubmed/9527404
  29. Saadat S, Beheshti F, Askari VR, Hosseini M, Mohamadian Roshan N, Boskabady MH. Aminoguanidine affects systemic and lung inflammation induced by lipopolysaccharide in rats. Respir Res. 2019 May 22; 20(1): 96. https://www.ncbi.nlm.nih.gov/pubmed/31113409. https://www.ncbi.nlm.nih.gov/pmc/articles/6530199. https://doi.org/10.1186/s12931-019-1054-6
  30. Bolton WK, Cattran DC, Williams ME, Adler SG, Appel GB, Cartwright K, et al. Randomized Trial of an Inhibitor of Formation of Advanced Glycation End Products in Diabetic Nephropathy. Am J Nephrol. 2004; 24: 32–40. https://www.ncbi.nlm.nih.gov/pubmed/14685005. https://doi.org/10.1159/000075627
  31. Kuznetsova VA, Soloveva OA, Matsevich AI, Spasov AA. Metod otsenki antiglikiruyuschey aktivnosti in vitro novyih veschestv. Volgogradskiy nauchno–meditsinskiy zhurnal. 2014; 3: 50–1. [Russian]
  32. Calderón–Ospina CA, Nava–Mesa MO. B Vitamins in the nervous system: Current knowledge of the biochemical modes of action and synergies of thiamine, pyridoxine, and cobalamin. CNS Neurosci Ther. 2019. Sep 6. https://www.ncbi.nlm.nih.gov/pubmed/31490017. https://doi.org/10.1111/cns.13207
  33. Ramis R, Ortega–Castro J, Caballero C, Casasnovas R, Cerrillo A, Vilanova B, et al. How Does Pyridoxamine Inhibit the Formation of Advanced Glycation End Products? The Role of Its Primary Antioxidant Activity. Antioxidants (Basel). 2019 Sep 1; 8(9): 344. https://doi.org/10.3390/antiox8090344
  34. Nascimento IBD, Dienstmann G, de Souza MLR, Fleig R, Hoffmann CBPC, Silva JC. Evaluation of Preeclampsia Results after Use of Metformin in Gestation: Systematic Review and Meta–analysis. Rev Bras Ginecol Obstet. 2018 Nov; 40(11): 713–21. https://www.ncbi.nlm.nih.gov/pubmed/30399639. https://doi.org/10.1055/s-0038-1675214
  35. Bailey CJ, Day C. Metformin: its botanical background. Pract Diab Int. 2004; 21(3): 115–7. https://doi.org/10.1002/pdi.606
  36. Anisimov VN. Molecular and physiological mechanisms of aging (2 tons). SPb: Science; 2008.
  37. Kim HG, Heo H, Sung MS, Park SW. Carnosine decreases retinal ganglion cell death in a mouse model of optic nerve crushing. Neurosci Lett. 2019 Aug 12; 711: 134431. https://www.ncbi.nlm.nih.gov/pubmed/31415801. https://doi.org/10.1016/j.neulet.2019.134431
  38. Arivazhagan P, Ramanathan K, Panneerselvam C. Effect of DL–α–lipoic acid on mitochondrial enzymes in aged rats. Chem Biol Interact. 2001; 138(2): 189–98. https://www.ncbi.nlm.nih.gov/pubmed/11672700. https://doi.org/10.1016/s0009-2797(01)00268-x
  39. Di Sotto A, Locatelli M, Macone A, Toniolo C, Cesa S, Carradori S, et al. Hypoglycemic, Antiglycation, and Cytoprotective Properties of a Phenol–Rich Extract From Waste Peel of Punica granatum L. var. Dente di Cavallo DC2. Molecules. 2019 Aug 27; 24(17): 3103. https://doi.org/10.3390/molecules24173103
  40. Belovol AN, Knyazkova II. Alfa–lipoevaya kislota: ot farmakologicheskih svoystv k klinicheskomu primeneniyu. Liki Ukrayini. 2015; 7(193): 4–9. [Russian]
  41. Yonei Y, Miyazaki R, Takahashi Y, Takahashi H, Nomoto K, Yagi M, et al. Anti–glycation effect of mixed herbal extract in individuals with pre–diabetes mellitus: a double–blind, placebo–controlled, parallel group study. J Anti–Aging Med. 2010; 7(5): 26–35. doi.org/10.3793/jaam.7.26
  42. Gkogkolou P, Böhm M. Advanced glycation end products: Key players in skin aging? Dermatoendocrinol. 2012; 4(3): 259–70. https://www.ncbi.nlm.nih.gov/pubmed/23467327. https://www.ncbi.nlm.nih.gov/pmc/articles/3583887. https://doi.org/10.4161/derm.22028
  43. Mendoza–Núñez VM, Arista–Ugalde TL, Rosado–Pérez J, Ruiz–Ramos M, Santiago–Osorio E. Hypoglycemic and antioxidant effect of Tai chi exercise training in older adults with metabolic syndrome. Clin Interv Aging. 2018 Apr 3; 13: 523–31. https://www.ncbi.nlm.nih.gov/pubmed/29662308. https://www.ncbi.nlm.nih.gov/pmc/articles/5892965. https://doi.org/10.2147/CIA.S157584