Inflammatory Metabolites of Arachidonic Acid in Tear Fluid in UV-Induced Corneal Damage

• Published in: Biochemistry (Moscow). Supplement. Series B, Biomedical chemistry Vol. 13; no. 3; pp. 264 - 270
• Main Authors: Chistyakov, D. V., Azbukina, N. V., Goriainov, S. V., Chistyakov, V. V., Gancharova, O. S., Tiulina, V. V., Baksheeva, V. E., Iomdina, E. N., Philippov, P. P., Sergeeva, M. G., Senin, I. I., Zernii, E. Yu
• Format: Journal Article
• Language: English
• Published: Moscow Pleiades Publishing 01.07.2019; Springer Nature B.V
• Subjects: Anterior chamber; Apoptosis; Arachidonate 12-lipoxygenase; Arachidonate 5-lipoxygenase; Arachidonic acid; Bioorganic Chemistry; Chemistry; Chemistry and Materials Science; Cornea; Edema; Epithelium; Feasibility studies; Inflammation; Keratitis; Lipid composition; Lipoxygenase; Medicinal Chemistry; Metabolic pathways; Metabolic rate; Metabolites; Prostaglandin D2; Prostaglandin D2 synthase; Prostaglandin E2; Ultraviolet radiation; keratitis; eicosanoids; tear film; 12-HETE; s: UV-induced corneal damage; prostaglandin E; prostaglandin D; 5-HETE; keratocyte apoptosis; 15d-PGJ
• ISSN: 1990-7508; 1990-7516
• DOI: 10.1134/S199075081903003X

— The ultraviolet (UV) B-induced damage of the eye surface of experimental animals (rabbits) includes total loss of corneal epithelium, apoptosis of keratocytes and stromal edema. These changes are accompanied by clinically and histologically manifested corneal inflammation, neutrophil infiltration, and exudation of the anterior chamber of the eye. According to results of mass spectrometric analysis, the UV-induced corneal damage is associated with pronounced changes in the tear lipid composition, including a decrease in the amount of arachidonic acid and prostaglandin E 2 and an increase in the concentrations of prostaglandin D 2 and its derivative 15d-PGJ 2 . In addition, it is accompanied by changes in the levels of hydroxyeicosate tetraenic acids, including a decrease of 12-HETE and an increase of 5-HETE. These changes suggest activation of metabolic pathways involving 5-lipoxygenase, 12-lipoxygenase, cyclooxygenases 1 and 2, and prostaglandin D synthase. These findings contribute to understanding mechanisms of UV-induced keratitis and point to feasibility of selective anti-inflammatory therapy for improving corneal regeneration after iatrogenic UV damage.