Riboflavin use as photoprotector in laser corneal refractive surgery

Cover Page


Cite item

Full Text

Abstract

The works of different authors on the role of riboflavin in the oxidative stress suppression in tissues and organs were analyzed. Experimental and clinical studies showed that the riboflavin (vitamin B2) has antioxidant properties and acts as a coenzyme for redox enzymes affecting the glutathione reduction. Russian scientists studies established a significant negative linear correlation between the level of malondialdehyde in blood serum and riboflavin consumption. Several studies showed that riboflavin deficiency affects the activity of antioxidant enzymes, including glucose peroxidase, superoxide dismutase and catalase, which leads to a reduction in tissue cells antioxidant potential. The riboflavin feasibility in laser refractive surgery is due to the development of oxidative stress in the cornea in response to the intervention and the need for its correction. In photorefractive corneal surgery, it is worsened by secondary ablation induced by ultraviolet radiation. Works of the last few years show that the oxidative effect of the radiation is attenuated when performing the excimer laser refractive ablation after presaturation of the stroma with riboflavin solution. Experimental studies showed that both drip and aerosol corneal saturation with 0.25% isotonic riboflavin solution does not affect the accuracy of excimer laser ablation of the corneal stroma. In the clinic, performing transepithelial photorefractive keratectomy with riboflavin photoprotection for myopia with astigmatism of varying degrees and without astigmatism minimized corneal syndrome, sterile inflammatory response. It accelerated epithelialization and was accompanied by early optometric indicators stabilization, which confirmed the feasibility of riboflavin use as photoprotector in laser corneal refractive surgery.

About the authors

A I Sultanova

National Ophthalmology Center named after Zarifa Aliyeva

Author for correspondence.
Email: rjafarova@bk.ru

References

  1. Бикбов М.М., Бикбова Г.М. Эктазии роговицы (патогенез, патоморфология, клиника, диагностика, лечение). М.: Офтальмология. 2011; 162 c.
  2. Корниловский И.М., Султанова А.И. Новые этапы развития технологии трансэпителиальной ФРК и её оптимизации на основе фотопротекции. Катарактальн. и рефракцион. хир. 2013; 13 (3): 15-19.
  3. Корниловский И.М., Султанова А.И., Миришова М.Ф., Бурцев А.А. Эффекты фотопротекции и кросслинкинга при новой технологии фоторефракционной абляции. Соврем. технол. в офтальмол. 2014; 14 (3): 161-163.
  4. Корниловский И.М., Султанова А.И., Миришова М.Ф., Сафарова А.Н. Первые клинические результаты лазерной рефракционной хирургии роговицы с фотопротекцией. Катарактальн. и рефракцион. хир. 2014; 14 (1): 21-25.
  5. Корниловский И.М., Бурцев А.А., Султанова А.И. и др. Трансэпителиальная ФРК с фотопротекцией и эффектом кросслинкинга. Катарактальн. и рефракцион. хир. 2015; 15 (3): 27-33.
  6. Султанова А.И., Миришова М.Ф. Эффект фотопротекции при рефракционной эксимерлазерной абляции роговицы, насыщенной рибофлавином. Oftalmologiya, elmi-praktik jurnal, Bakı. 2014; 14 (3): 84-87.
  7. Alio J.L., Javaloy J. Corneal inflammation following corneal photoablative refractive surgery with excimer laser. Surv. Ophthalmol. 2013; 58: 11-25. http://dx.doi.org/10.1016/j.survophthal.2012.04.005
  8. Ambrosio G., Flaherty J.T., Duilio C. et al. Oxygen radicals generated at reflow induce peroxidation of membrane lipids in reperfused hearts. J. Clin. Invest. 1991; 87: 2056-2206. http://dx.doi.org/10.1172/JCI115236
  9. Ashoori M., Saedisomeolia A. Riboflavin (vitamin B2) and oxidative stress: a review. Brit. J. Nutr. 2014; III: 1985-1991. http://dx.doi.org/10.1017/S0007114514000178
  10. Bates J. Glutathione and related indices in rat lenses, liver and red cells dring riboflavin deficiency and its correction. Exp. Eye Res. 1991; 53: 123-130. http://dx.doi.org/10.1016/0014-4835(91)90154-7
  11. Betz A.L., Ren X.D., Ennis S.R. et al. Riboflavin reduces edema in focal cerebral ischemia. Acta Neurochir. Suppl. (Wien). 1994; 60: 314-317. http://dx.doi.org/10.1007/978-3-7091-9334-1_84
  12. Bolli R., Zughaib M., Li X.Y. et al. Recurrent ischemia in the canine heart causes recurrent bursts of free radical production that have a cumulative effect on contractile function. A pathophysiological basis for chronic myocardial «stunning». J. Clin. Invest. 1995; 96:1066-1084. http://dx.doi.org/10.1172/JCI118093
  13. Brady P.S., Brady L.J., Parsons M.J., et al. Effects of riboflavin deficiency on growth and glutathione peroxidase system enzymes in the baby pig. J. Nutr. 1979; 109: 1615-1622.
  14. Carden D.L., Granger D.N. Pathophysiology of ischaemia-reperfusion injury. J. Pathol. 2000; 190: 255-266. http://dx.doi.org/10.1002/(SICI)1096-9896(200002)190:3<255::AID-PATH526>3.0.CO;2-6
  15. Cohen D., Chuk R., Berman G. Et al. Ablation spectra of human cornea. J. Biomed. Opt. 2001; 6 (3): 339-343. http://dx.doi.org/10.1117/1.1380670
  16. Christensen H.N. Riboflavin can protect tissue from oxidative injury. Nutr. Rev. 1993; 51: 149-150.
  17. Das B.S., Thurnham D.I., Patnaik J.K. et al. Increased plasma lipid peroxidation in riboflavin-deficient, malaria infected children. Am. J. Clin. Nutr. 1990; 51: 859-863.
  18. Dutta P., Rivlin R.S., Pinto J. Enhanced depletion of lens reduced glutathione Adriamycin in riboflavin-deficient rats. Biochem. Pharmacol. 1990; 40: 1111-1115. http://dx.doi.org/10.1016/0006-2952(90)90500-K
  19. Hayes J.D., McLellan L.I. Glutathione and glutathionedependent enzymes represent a co-ordinately regulated defence against oxidative stress. Free Radic. Res. 1999; 31: 273-300. http://dx.doi.org/10.1080/10715769900300851
  20. Hirano H., Hamajima S., Horiuchi S. et al. Effects of B2-deficiency on lipoperoxide and its scavenging system in the rat lens. Int. J. Vitam. Nutr. Res. 1983; 53: 377-382.
  21. Horiuchi S., Hirano H., Ono S. Reduced and oxidized glutathione concentrations in the lenses of riboflavindeficient rats. J. Nutr. Sci. Vitaminol. (Tokyo). 1984; 30: 401-403. http://dx.doi.org/10.3177/jnsv.30.401
  22. Huang J., Tian L., Wu X. et al. Effects of dietary riboflavin levels on antioxidant defense of the juvenile grouper Epinephelus coioides. Fish Physiol. Biochem. 2010; 36: 55-62. http://dx.doi.org/10.1007/s10695-008-9279-1
  23. Iwanaga K., Hasegawa T., Hultquist D.E. et al. Riboflavin-mediated reduction of oxidant injury, rejection, and vasculopathy after cardiac allotransplantation. Transplantation. 2007; 83: 747-753. http://dx.doi.org/10.1097/01.tp.0000256283.06469.d4
  24. George B.O., Ojegbemi O. Oxidative stress and the effect of riboflavin supplementation in individuals with uncomplicated malaria infection. J. Biotechnol. 2009; 8: 849-853.
  25. Kaplowitz N., Aw T.Y., Ookhtens M. The regulation of hepatic glutathione. Annu. Rev. Pharmacol. Toxicol. 1985; 25: 715-744. http://dx.doi.org/10.1146/annurev.pa.25.040185.003435
  26. Kodentsova V.M., Vrzhesinskaia O.A., Beketova N.A. et al. The connection between vitamin and antioxidant status of the children with decreased hemoglobin level. Vopr. Pitan. 2003; 72: 3-7.
  27. Kukielka G.L., Smith C.W., Manning A.M. et al. Induction of interleukin-6 synthesis in the myocardium. Potential role in postreperfusion inflammatory injury. Circulation. 1995; 92: 1866-1875. http://dx.doi.org/10.1161/01.CIR.92.7.1866
  28. Lee S.S., Ye J.H., Jones D.P. et al. Correlation of H2O2 production and liver catalase during riboflavin deficiency and repletion in mammals. Biochem. Biophys. Res. Commun. 1983; 117: 788-793. http://dx.doi.org/10.1016/0006-291X(83)91666-2
  29. Liang H., Liu Q., Xu J. The effect of riboflavin on lipid peroxidation in rats. Wei. Sheng Yan Jiu. 1999; 28: 370-371.
  30. Mack C.P., Hultquist D.E., Shlafer M. Myocardial flavin reductase and riboflavin: a potential role in decreasing reoxygenation injury. Biochem. Biophys. Res. Commun. 1995; 212: 35-40. http://dx.doi.org/10.1006/bbrc.1995.1932
  31. Mulherin D.M., Thurnham D.I., Situnayake R.D. Glutathione reductase activity, riboflavin status, and disease activity in rheumatoid arthritis. Ann. Rheum. Dis. 1996; 55: 837-840. http://dx.doi.org/10.1136/ard.55.11.837
  32. Padayatty S.J., Katz A., Wang Y. et al. Vitamin C as an antioxidant: evaluation of its role in disease prevention. J. Am. Coll. Nutr. 2003; 22: 18-35. http://dx.doi.org/10.1080/07315724.2003.10719272
  33. Powers H.J., Thurnham D.I. Riboflavin deficiency in man: effects on haemoglobin and reduced glutathione in erythrocytes of different ages. Br. J. Nutr. 1981; 46: 257-266. http://dx.doi.org/10.1079/BJN19810031
  34. Rao P.V., Bhat K.S. Influence dietary riboflavin deficiency on lenticular glutathione redox cycle, lipid peroxidation, and free radical scavengers in the rat. J. Clin. Biochem. Nutr. 1989; 6: 195-204. http://dx.doi.org/10.3164/jcbn.6.195
  35. Rogers K.M., Augusteyn R.C. Glutathione reductase in normal and cataractous human lenses. Exp. Eye Res. 1978; 27: 719-721. http://dx.doi.org/10.1016/0014-4835(78)90041-6
  36. Seekamp A., Hultquist D.E., Till G.O. Protection by vitamin B2 against oxidant-mediated acute lung injury. Inflammation. 1999; 23: 449-460. http://dx.doi.org/10.1023/A:1021965026580
  37. Sherif A.M. Accelerated versus conventional corneal collagen cross-linking in treatment of mild keratoconus: a comparative study. Clin. Ophthalmol. 2014; 8: 1435-1440. http://dx.doi.org/10.2147/OPTH.S59840
  38. Taniguchi M., Hara T. Effects of riboflavin and selenium deficiencies on glutathione and its relating enzyme activities with respect to lipid peroxide content of rat livers. J. Nutr. Sci. Vitaminol. (Tokyo). 1983; 29: 283-292. http://dx.doi.org/10.3177/jnsv.29.283
  39. Tomas-Juan J., Murueta-Goyena Larrañaga A., Hanneken L. Corneal regeneration after photorefractive keratectomy: a review. J. Optom. 2015; 8 (3): 149-169. http://dx.doi.org/10.1016/j.optom.2014.09.001
  40. Tuft S., Al-Dhahir R., Dyer P., Zahao Z. Characterization of fluorescence spectra produced by excimer laser irradiation of cornea. Invest. Ophthalmol. Vis. Sci. 1989; 31: 1512-1518.
  41. Tumkiratiwong P., Tungtrongchitr R., Migasena P. et al. Antioxidant enzyme levels in the erythrocytes of riboflavindeficient and Trichinella spiralis-infected rats. Southeast Asian J. Trop. Med. Public Health. 2003; 34: 480-485.
  42. Traber M.G., Atkinson J. Vitamin E, antioxidant and nothing more. Free Radic. Biol. Med. 2007; 43: 4-15. http://dx.doi.org/10.1016/j.freeradbiomed.2007.03.024
  43. Wang G., Li W., Lu X. et al. Riboflavin alleviates cardiac failure in type I diabetic cardiomyopathy. Heart Int. 2011; 6: 21. http://dx.doi.org/10.4081/hi.2011.e21
  44. Wang S., Mei J., Chen Q. et al. Effect of beta-carotene and riboflavin on lipid peroxidation in rats. Acta Nutr. Sin. 1999; 21: 22-27.
  45. Young A.J., Lowe G.M. Antioxidant and prooxidant properties of carotenoids. Arch. Biochem. Biophys. 2001; 385: 20-27. http://dx.doi.org/10.1006/abbi.2000.2149

Supplementary files

Supplementary Files
Action
1. JATS XML

© 2016 Sultanova A.I.

Creative Commons License

This work is licensed
under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.





This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies