Correlations of parameters of the oxidative-antioxidative system in the lens, aqueous humor and tear fluid with the grade of lens opacity in rabbits with cataract and/or bacterial keratitis: an experimental study

Authors

  • V. Ia. Usov Petro Mohyla Black Sea National University, Mykolaiv, Ukraine
  • Tarik Abou Tarboush SI "The Filatov Institute of Eye Diseases and Tissue Therapy of the NAMS of Ukraine; Odesa, Ukraine
  • S. G. Kolomiichuk SI "The Filatov Institute of Eye Diseases and Tissue Therapy of the NAMS of Ukraine"

DOI:

https://doi.org/10.31288/oftalmolzh202524957

Keywords:

cataract, keratitis, lipid peroxidation, antioxidant enzymes, methyl-ethyl pyridinol hydrochloride, lens, cornea, experiment

Abstract

Purpose: To determine correlations of the parameters of the oxidative-anti-oxidative system in the lens, aqueous humor and tear fluid with the grade of lens opacity in rabbits with cataract and/or bacterial keratitis treated versus not treated with methyl-ethyl pyridinol hydrochloride (MH).
Methods: Fifty-four adult Chinchilla rabbits were used for all experiments. Superficial bacterial keratitis only was induced only in the right eye (groups 1 and 2), and each of animals in group 2 received five four-week cycles of four-times-a-day-treatment with MH in the right eye separated by four-week breaks. In animals of groups 3 and 4, cataract was induced by nine-hours-a-day total exposure to 350-1150 nm ultraviolet (UV) radiation from a mercury-arc lamp for a period 40 weeks. Each of animals in group 4 received MH treatment in both eyes using the same scheme as noted above. In animals of groups 5 and 6, cataract was induced in the same way as in animals of group 3, and keratitis was induced in the same way as in animals of group 1. Each of animals in group 6 received MH treatment in the right eye using the same scheme as noted above. Group 7 comprised intact control rabbits. The Spearmen rank correlation was used to assess associations between the grade of lens opacity, activities of glutathione peroxidase (GP) and catalase (CT), and levels of malondialdehyde (MDA) and diene conjugate (DC).
Results: The grade of lens opacity was negatively correlated with the activities of GP and CT, and positively correlated with the levels of lipid peroxidation products (MDA and DC) for rabbits with keratitis only, cataract only, and especially keratitis plus cataract, treated or not treated with MH. There was no substantial change in the values of correlation coefficients for rabbits treated with MH compared to those not treated with MH.
Conclusion: Our findings of correlations between the above-mentioned parameters indicate the important role the metabolic abnormalities have in the formation of structural and functional changes in the lens of animals with corneal inflammation. These findings also lay ground for introducing pathogenesis-targeted metabolic correction with MH for oxidative-antioxidative system imbalance in ocular tissues

References

Kumari R. Senile Cataract. J Community Med Health Solut. 2024; 5: 001-007. https://doi.org/10.29328/journal.jcmhs.1001041

Li J, Buonfiglio F, Zeng Y, Pfeiffer N, Gericke A. Oxidative Stress in Cataract Formation: Is There a Treatment Approach on the Horizon? Antioxidants. 2024; 13(10):1249. https://doi.org/10.3390/antiox13101249

Imelda E, Idroes R, Khairan K, Lubis RR, Abas AH, Nursalim AJ, et al. Natural Antioxidant Activities of Plants in Preventing Cataractogenesis. Antioxidants. 2022; 11(7):1285. https://doi.org/10.3390/antiox11071285

Maltry AC, Cameron JD. Pathology of the Lens. In: Albert DM, Miller JW, Azar DT, Young LH (eds). Albert and Jakobiec's Principles and Practice of Ophthalmology. Springer, Cham. 2022. https://doi.org/10.1007/978-3-030-42634-7_137

Cicinelli MV, Buchan JC, Nicholson M, Varadaraj V, Khanna RC. Cataracts. Lancet. 2023;401(10374):377-389. https://doi.org/10.1016/S0140-6736(22)01839-6

Liu S, Jin Z, Xia R, Zheng Z, Zha Y, Wang Q, et al. Protection of Human Lens Epithelial Cells from Oxidative Stress Damage and Cell Apoptosis by KGF-2 through the Akt/Nrf2/HO-1 Pathway. Oxid Med Cell Longev.2022;6933812. https://doi.org/10.1155/2022/6933812

Lim JC, Jiang L, Lust NG, Donaldson PJ. Minimizing Oxidative Stress in the Lens: Alternative Measures for Elevating Glutathione in the Lens to Protect against Cataract. Antioxidants. 2024; 13(10):1193. https://doi.org/10.3390/antiox13101193

Cejka C, Cejkova J. Oxidative stress to the cornea, changes in corneal optical properties, and advances in treatment of corneal oxidative injuries. Oxid Med Cell Longev. 2015;591530. https://doi.org/10.1155/2015/591530

Nita M, Grzybowski A. The Role of the Reactive Oxygen Species and Oxidative Stress in the Pathomechanism of the Age-Related Ocular Diseases and Other Pathologies of the Anterior and Posterior Eye Segments in Adults. Oxid Med Cell Longev. 2016;3164734. https://doi.org/10.1155/2016/3164734

Nien, CW., Lee, CY., Chen, HC. et al. The elevated risk of sight-threatening cataract in diabetes with retinopathy: a retrospective population-based cohort study. BMC Ophthalmol.2021;21, 349. https://doi.org/10.1186/s12886-021-02114-y

Cejka C, Cejkova J. Oxidative stress to the cornea, changes in corneal optical properties, and advances in treatment of corneal oxidative injuries. Oxid Med Cell Longev. 2015;591530. https://doi.org/10.1155/2015/591530

Nita M, Grzybowski A. The Role of the Reactive Oxygen Species and Oxidative Stress in the Pathomechanism of the Age-Related Ocular Diseases and Other Pathologies of the Anterior and Posterior Eye Segments in Adults.Oxid Med Cell Longev.2016;3164734. https://doi.org/10.1155/2016/3164734

Álvarez-Barrios A, Álvarez L, García M, Artime E, Pereiro R, González-Iglesias H. Antioxidant Defenses in the Human Eye: A Focus on Metallothioneins. Antioxidants (Basel). 2021;10(1):89. https://doi.org/10.3390/antiox10010089

Gilger BC. How study of naturally occurring ocular disease in animals improves ocular health globally. J Am Vet Med Assoc. 2022;260(15):1887-1893. https://doi.org/10.2460/javma.22.08.0383

Lotti R, Dart JK. Cataract as a complication of severe microbial keratitis. Eye (Lond). 1992;6(Pt 4):400-3. https://doi.org/10.1038/eye.1992.82

Ting DSJ, Cairns J, Gopal BP, Ho CS, Krstic L, Elsahn A, Lister M, Said DG, Dua HS. Risk Factors, Clinical Outcomes, and Prognostic Factors of Bacterial Keratitis: The Nottingham Infectious Keratitis Study. Front Med (Lausanne). 2021;8:715118. https://doi.org/10.3389/fmed.2021.715118

Usov Via, Tarik Abou Tarboush. [Features of the development of experimental cataract in the presence of induced corneal inflammation]. Oftalmol Zh. 2010;6:66-70. Russian.

Usov Via, Tarik Abou Tarboush, Kondratieva EI. [Impact of emoksipin on the development of experimental cataract in animals with keratitis]. Oftalmol Zh. 2011;2:49-54. Russian.

Usov Via, Tarik Abou Tarboush, Kondratieva EI. [Corrective impact of emoksipin on peroxidation in the lens, aqueous humor and tear fluid in animals with experimental keratitis and exposure to light]. Oftalmol Zh. 2011;3:65-70. Russian.

Brown NA, Bron AJ, Ayliffe W, Sparrow J, Hill AR. The objective assessment of cataract. Eye (Lond). 1987;1 (Pt 2):234-246. https://doi.org/10.1038/eye.1987.43

Miot HA. Correlation analysis in clinical and experimental studies. JVasc Bras. 2018;17(4):275-279. https://doi.org/10.1590/1677-5449.174118

Quinlan RA, Clark JI. Insights into the biochemical and biophysical mechanisms mediating the longevity of the transparent optics of the eye lens. J Biol Chem. 2022;298(11):102537. https://doi.org/10.1016/j.jbc.2022.102537

Wang Y, Grenell A, Zhong F, Yam M, Hauer A, Gregor E, et al. Metabolic signature of the aging eye in mice. Neurobiol Aging. 2018;71:223-233. https://doi.org/10.1016/j.neurobiolaging.2018.07.024

Shrestha GS, Vijay AK, Stapleton F, White A, Pickford R, Carnt N. Human tear metabolites associated with nucleoside-signalling pathways in bacterial keratitis. Exp Eye Res. 2023;228:109409. https://doi.org/10.1016/j.exer.2023.109409

Iacubitschii M, Bendelic E, Alsaleim S. Aqueous humor's biochemical composition in ocular pathologies. Mold Med J. 2019;62(2):38-43.doi: 10.5281/zenodo.3233928.

Zhang Y, Liang Q, Liu Y, Pan Z, Baudouin C, Labbé A, Lu Q. Expression of cytokines in aqueous humor from fungal keratitis patients. BMC Ophthalmol. 2018;18(1):105. https://doi.org/10.1186/s12886-018-0754-x

TsaoY-T, WuW-C, ChenK-J, LiuC-F, HsuehY-J, ChengC-M, et al. An Assessment of Cataract Severity Based on Antioxidant Status and Ascorbic Acid Levels in Aqueous Humor. Antioxidants. 2022; 11(2):397. https://doi.org/10.3390/antiox11020397

Forte G, Battagliola ET, Malvasi M et al. Trace Element Concentration in the Blood and Aqueous Humor of Subjects with Eye Cataract. Biol Trace Elem Res. 2025; 203:684-693. https://doi.org/10.1007/s12011-024-04207-3

Winiarczyk M, Biela K, Michalak K, Winiarczyk D, Mackiewicz J. Changes in Tear Proteomic Profile in Ocular Diseases. Int J Environ Res Public Health. 2022; 19(20):13341. https://doi.org/10.3390/ijerph192013341

Tessem M-B, Bathen T F, Čejková J, Midelfart A. Effect of UV-A and UV-B irradiation on the metabolic profile of aqueous humor in rabbits analyzed by 1H NMR spectroscopy. Invest Ophthalmol Vis Sci. 2005;46(3):776-781. https://doi.org/10.1167/iovs.04-0787

Zhen-Zhen Liu, Shao-Fan Chen, Tong-Yong Yu, Guo-Shu Ma, Xiang-Yu Huang,De-Ying Yu, et al. Effects of sunlight on the eye. Int Eye Res. 2021;2(1). https://doi.org/10.18240/ier.2021.01.10

Kulbay M, Wu KY, Nirwal GK, Bélanger P, Tran SD. Oxidative Stress and Cataract Formation: Evaluating the Efficacy of Antioxidant Therapies. Biomolecules. 2024;14(9):1055. https://doi.org/10.3390/biom14091055

Srinivasan M, Ravindran RD, O'Brien KSet al. Antioxidant vitamins for cataracts: 15-year follow-up of a randomized trial. Ophthalmology.2020;127(7): 986-987. https://doi.org/10.1016/j.ophtha.2020.01.050

Braakhuis AJ, Donaldson CI, Lim JC, Donaldson PJ. Nutritional Strategies to Prevent Lens Cataract: Current Status and Future Strategies. Nutrients. 2019; 11(5):1186. https://doi.org/10.3390/nu11051186

Imelda E, Idroes R, Khairan K, Lubis RR, Abas AH, Nursalim AJ, et al. Natural Antioxidant Activities of Plants in Preventing Cataractogenesis.Antioxidants.2022;11(7):1285. https://doi.org/10.3390/antiox11071285

Serebryany E, Chowdhury S, Woods Ch Net al. A native chemical chaperone in the human eye lens. eLife. 2022;11:e76923. https://doi.org/10.7554/eLife.76923

Li J, Buonfiglio F, Zeng Y, Pfeiffer N, Gericke A. Oxidative Stress in Cataract Formation: Is There a Treatment Approach on the Horizon? Antioxidants. 2024;13(10):1249. https://doi.org/10.3390/antiox13101249

Wang L, Li X, Men X, Liu X,LuoJ. Research progress on antioxidants and protein aggregationinhibitors in cataract prevention and therapy (Review). Mol Med. 2025;31:22. https://doi.org/10.3892/mmr.2024.13387

Published

2025-04-30

How to Cite

1.
Usov VI, Tarboush TA, Kolomiichuk SG. Correlations of parameters of the oxidative-antioxidative system in the lens, aqueous humor and tear fluid with the grade of lens opacity in rabbits with cataract and/or bacterial keratitis: an experimental study. J.ophthalmol. (Ukraine) [Internet]. 2025 Apr. 30 [cited 2025 May 7];(2):49-57. Available from: https://ua.ozhurnal.com/index.php/files/article/view/222

Issue

Section

Experimental Studies