Cellular composition of an experimental chemical injury to the cornea after exposure to PEGylated hyaluronidase and subtilisin enzymes
https://doi.org/10.31549/2542-1174-2023-7-1-89-109
Abstract
Introduction. Under conditions of chemical damage to the cornea, its cellular structure is significantly disrupted, requiring emergency highly differentiated regeneration without an expressed proliferative component of inflammation and expansion of immunocompetent cells to gain an antimicrobial potential. For the purpose of pharmacological initiation of these processes, the study of the topical administration of anti-inflammatory enzyme preparations, such as subtilisin and hyaluronidase, is pathogenetically justified.
Aim. To study the effect of hyaluronidase and subtilisin, PEGylated (polyethylene glycol – PEG) using the technology of electron beam synthesis on the number of immunocompetent cells in the area of the corneal chemical injury during their subconjunctival and topical administration.
Materials and methods. An experimental study of the effect of PEGylated hyaluronidase and subtilisin enzymes, on the cellular composition of the corneal chemical injury was performed on 28 rabbits. Corneal injury was modeled using the Obenberger alkali burn technique. PEG-subtilisin or PEG-hyaluronidase was applied topically or subconjunctivally into the right eye of the animal, depending on the group, the left eye of the animal was used as a control – it was treated with 0.9% NaCl. After the experiment, enucleation was performed. The biomaterial obtained was used to prepare tissue specimens for morphological examination.
Results. The total count of cells in the groups of topical and subconjunctival administration of PEG-subtilisin was 43 (40; 52) and 73 (33; 92), and subconjunctival injection of PEG-hyaluronidase – 46 (37; 61), which was higher than the count of cells when using 0.9% NaCl in these groups (p < 0.01) and higher (p < 0.0001) cell numbers in the group of topical administration of PEG-hyaluronidase. The total count of cells with topical application of PEG-hyaluronidase was 15 (13; 16), with topical application of 0.9% NaCl of this group – also 15 (14; 18) (p = 0.38). The neutrophil count with the use of PEG-subtilisin was 1 (1; 2) with topical and 0 (0; 1) with subconjunctival administration, and with the use of PEG-hyaluronidase – 0 (0; 0) both with topical and subconjunctival administration.
Conclusion. The administration of PEG-hyaluronidase subconjunctivally and PEG-subtilisin both topically and subconjunctivally leads to an increased migration of immunocompetent cells to the area of the corneal chemical injury, while the migration of neutrophils is insignificant. It is completely absent when PEG-hyaluronidase is injected subconjunctivally. Topical administration of PEG-hyaluronidase does not induce a pronounced cellular response of immunocompetent cells in the area of the corneal chemical injury, and the effect of the application is comparable to that of 0.9% NaCl.
About the Authors
V. E. ZabanovaRussian Federation
Viktoriya E. Zabanova – Assistant, Department of Ophthalmology; Junior Researcher, Laboratory of Experimental and Clinical Pharmacology
52, Krasny prosp., Novosibirsk, 630091
K. I. Ershov
Russian Federation
Konstantin I. Ershov – Cand. Sci. (Bio.), Associate Professor, Department of Pharmacology, Clinical Pharmacology and Evidence-Based Medicine; Researcher, Laboratory of Pharmaceutical Technology
Novosibirsk
M. S. Selyakova
Russian Federation
Maria S. Selyakova – Cand. Sci. (Med.), Senior Lecturer, Department of Pathological Anatomy
Novosibirsk
N. P. Leonov
Russian Federation
Nikolai P. Leonov – Cand. Sci. (Med.), Researcher, Laboratory of Pharmaceutical Technology
Novosibirsk
G. I. Baykalov
Russian Federation
German I. Baykalov – Resident, Department of Pharmacology, Clinical Pharmacology and Evidence-Based Medicine; Junior Researcher, Laboratory of Pharmacological Modeling and Screening of Bioactive Molecules
Novosibirsk
A. Zh. Fursova
Russian Federation
Anzhella Zh. Fursova – Dr. Sci. (Med.), Associate Professor, Head, Department of Ophthalmology; Leading Researcher
Novosibirsk
A. P. Nadeev
Russian Federation
Aleksander P. Nadeev – Dr. Sci. (Med.), Professor, Head, Department of Pathological Anatomy
Novosibirsk
P. G. Madonov
Russian Federation
Pavel G. Madonov – Dr. Sci. (Med.), Associate Professor, Head, Department of Pharmacology, Clinical Pharmacology and Evidence-Based Medicine; Head, Department of Experimental Pharmacology, Institute of Clinical and Experimental Lymphology
Novosibirsk
References
1. Chen C.C., Manning A.M. TGF-beta 1, IL-10 and IL-4 differentially modulate the cytokine-induced expression of IL-6 and IL-8 in human endothelial cells. Cytokine. 1996;8(1):58–65. DOI: 10.1006/cyto.1995.0008.
2. Nakamura M., Nishida T. Differential Effects of epidermal growth factor and interleukin 6 on corneal epithelial cells and vascular endothelial cells. Cornea. 1999;18(4):452-458. DOI: 10.1097/00003226-199907000-00011.
3. Ebihara N., Matsuda A., Nakamura S., Matsuda H., Murakami A. Role of the IL-6 classic- and trans-signaling pathways in corneal sterile Inflammation and wound healing. Invest. Ophthalmol. Vis. Sci. 2011;52(12):8549-8557. DOI: 10.1167/iovs.11-7956.
4. Hafezi F., Gatzioufas Z., Angunawela R., Ittner LM. Absence of IL-6 prevents corneal wound healing after deep excimer laser ablation in vivo. Eye (Lond). 2018;32(1):156-157. DOI: 10.1038/eye.2017.238.
5. Wilson S.E. Corneal wound healing. Exp. Eye Res. 2020;197:108089. DOI: 10.1016/j.exer.2020.108089.
6. Bubnova N.A., Sternin Yu.I. (2011). Systemic Enzyme Therapy in Surgical Practice: Manual for Doctors. Saint Petersburg. 44 p. (In Russ.)
7. Lysikova M., Wald M., Masinovsky Z. The mechanisms of the Inflammatory response and the impact on them using proteolytic enzymes. Cytokines and Inflammation. 2004;3(3):48-53. (In Russ.)
8. Madonov P.G., Mishenina S.V., Kinsht D.N., Kikhtenko N.V. Chemical and pharmacological properties of subtilisins. The Siberian Scientific Medical Journal. 2016;36(3):13–22. (In Russ.)
9. Omura K., Hitosugi M., Zhu X. et al. A newly derived protein from Bacillus subtilis natto with both antithrombotic and fibrinolytic effects. J. Pharmacol. Sci. 2005;99(3):247-251. DOI: 10.1254/jphs.fp0050408.
10. Madonov P.G., Mishenina S.V., Kinsht D.N., Kikhtenko N.V. Targeted pharmacodynamic of subtilisins. The Siberian Scientific Medical Journal. 2016;36(4):15-24. (In Russ.)
11. Dygay А.М., Pershina О.V., Krupin V.A. et al. Study of antyfibrotic activity of modified and native hyaluroni-dase at pulmonary fibrosis. The Siberian Scientific Medical Journal. 2017;37(4):5-10. (In Russ.)
12. Ermolaeva L.A., Fomina T.I., Dubskaya T.Yu. et al. (2017). Safety study and assessment of the local irritation effect of a pharmacological substance based on poloxamer-hyaluronate-endo-B-N-acetylhexosaminidase with multiple endotracheal administration. In Current Drug Toxicology: Essential and Practical Aspects. Proceedings of the 2nd All Russian Scientific Conference (Tomsk, 13–15 june 2017) / ed. А.М. Dygay. Tomsk. P. 11. (In Russ.)
13. Skurihin E.G., Pershina O.V., Krupin V.A. et al. Effects and mechanism of pegylated hyaluronidaze in C57BL/6 mice under bleomycin induced pulmonary fibrosis. Pathogenesis. 2015;13(3):56-64. (In Russ.)
14. Skurikhin E.G., Pershina O.V., Reztsova A.M. et al. Modulation of bleomycin-induced lung fibrosis by pegylated hyaluronidase and dopamine receptor antagonist in mice. PLoS One. 2015;10(4):е0125065. DOI: 10.1371/journal.pone.0125065.
15. Dygay A.M., Zyuz’kov G.N., Zhdanov V.V. et al. Specific activity of electron-beam synthesis immobilized hyaluronidase on G-CSF induced mobilization of bone marrow progenitor cells. Stem Cell Rev. Rep. 2013;9(2):140-147. DOI: 10.1007/s12015-012-9423-2.
16. Mccann M. Intravenous hyaluronidase for visual loss secondary to filler injection: a novel therapeutic approach. J. Clin. Aesthet. Dermatol. 2019;12(12):25-27.
17. Pereira P.A.T., Bitencourt C.S., Reis M.B. et al. Immunomodulatory activity of hyaluronidase is associated with metabolic adaptations during acute Inflammation. Inflamm. Res. 2020;69(1):105-113. DOI: 10.1007/s00011-019-01297-x.
18. Kalandar A., Williams J., Lalonde D. Can we restore vision? A cadaveric study using hyaluronidase for retinal artery occlusion. Plast. Reconstr. Surg. Glob. Open. 2019;7(9):e2412. DOI: 10.1097/GOX.0000000000002412.
19. Washington P.M., Lee C., Dwyer M.K.R. et al. Hyaluronidase reduced edema after experimental traumatic brain injury. J. Cereb. Blood Flow Metab. 2019;40(10):271678X19882780. DOI: 10.1177/0271678X19882780.
20. Dygay A.M., Artamonov A.V., Bekarev A.A. et al. (2011). Nanotechnologies in Pharmacology. Moscow. 136 p. (In Russ.)
21. Madonov P.G., Ershov K.I., Dubrovin A.V. et al. Electron-beam modification of preparations of the albuminous nature for improvement of their pharmacological properties. Medicine and Education in Siberia. 2013;4:83. (In Russ.)
22. Obenberger J. Paper strips and rings as simple tools for standartization of experimental eye injuries. Ophthalmol. Res. 1975;7:363-366.
Review
For citations:
Zabanova V.E., Ershov K.I., Selyakova M.S., Leonov N.P., Baykalov G.I., Fursova A.Zh., Nadeev A.P., Madonov P.G. Cellular composition of an experimental chemical injury to the cornea after exposure to PEGylated hyaluronidase and subtilisin enzymes. Journal of Siberian Medical Sciences. 2023;(1):89-109. https://doi.org/10.31549/2542-1174-2023-7-1-89-109