Mechanisms of perioperative corneal abrasions: Alterations in the tear film proteome


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Abstract

Perioperative corneal abrasion is a common ophthalmic complication detectable in patients undergoing general anesthesia. In this study, using experimental perioperative corneal abrasion in animals (rabbits) correlations have been found between development of corneal abrasion and proteomic changes in the tear film. The process of accumulation of pathological changes in the cornea begins after 1 h of general anesthesia while after 3–6 h of general anesthesia clinically manifested abrasions have been recognized. The development of corneal abrasions was associated with different changes in the content of the major proteins of the tear film. Analysis of the tear proteome points to suppressed lachrymal gland functioning, and suggests that serotransferrin, serum albumin and annexin A1 may be applicable as potential tear markers of the ophthalmic complication. The biochemical changes in the tear film included the rapid decrease in total antioxidant activity and activity of superoxide dismutase, as well as the decrease in interleukin-4 and the increase in interleukin-6 content thus indicating development of oxidative and pro-inflammatory responses. These findings suggest that antioxidant and anti-inflammatory therapy is a prospective approach for prevention/treatment of perioperative corneal abrasions. The observed anesthesia-induced effects should be taken into consideration in any study of ocular surface diseases employing anesthetized animals.

About the authors

E. Yu. Zernii

Belozersky Institute of Physico-Chemical Biology

Author for correspondence.
Email: zerni@belozersky.msu.ru
Russian Federation, Leninskye gory bld. 1-40, Moscow, 119992

O. S. Gancharova

Belozersky Institute of Physico-Chemical Biology

Email: senin@belozersky.msu.ru
Russian Federation, Leninskye gory bld. 1-40, Moscow, 119992

I. E. Ishutina

Skryabin Moscow State Academy of Veterinary Medicine and Biotechnology

Email: senin@belozersky.msu.ru
Russian Federation, ul. Akademika Skryabina 23, Moscow, 109472

V. E. Baksheeva

Belozersky Institute of Physico-Chemical Biology

Email: senin@belozersky.msu.ru
Russian Federation, Leninskye gory bld. 1-40, Moscow, 119992

M. O. Golovastova

Belozersky Institute of Physico-Chemical Biology

Email: senin@belozersky.msu.ru
Russian Federation, Leninskye gory bld. 1-40, Moscow, 119992

E. I. Kabanova

Skryabin Moscow State Academy of Veterinary Medicine and Biotechnology

Email: senin@belozersky.msu.ru
Russian Federation, ul. Akademika Skryabina 23, Moscow, 109472

M. S. Savchenko

Belozersky Institute of Physico-Chemical Biology

Email: senin@belozersky.msu.ru
Russian Federation, Leninskye gory bld. 1-40, Moscow, 119992

M. V. Serebryakova

Belozersky Institute of Physico-Chemical Biology

Email: senin@belozersky.msu.ru
Russian Federation, Leninskye gory bld. 1-40, Moscow, 119992

L. F. Sotnikova

Skryabin Moscow State Academy of Veterinary Medicine and Biotechnology

Email: senin@belozersky.msu.ru
Russian Federation, ul. Akademika Skryabina 23, Moscow, 109472

A. A. Zamyatnin

Belozersky Institute of Physico-Chemical Biology; Institute of Molecular Medicine

Email: senin@belozersky.msu.ru
Russian Federation, Leninskye gory bld. 1-40, Moscow, 119992; ul. Trubetskaya 8, Moscow, 119991

P. P. Philippov

Belozersky Institute of Physico-Chemical Biology

Email: senin@belozersky.msu.ru
Russian Federation, Leninskye gory bld. 1-40, Moscow, 119992

I. I. Senin

Belozersky Institute of Physico-Chemical Biology

Author for correspondence.
Email: senin@belozersky.msu.ru
Russian Federation, Leninskye gory bld. 1-40, Moscow, 119992

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