Alterations in Tear Content of Inflammatory Oxylipines Associated with Perioperative Dry Eye Syndrome

• Published in: Biochemistry (Moscow). Supplement series A, Membrane and cell biology Vol. 14; no. 2; pp. 134 - 139
• Main Authors: Chistyakov, D. V., Azbukina, N. V., Astakhova, A. A., Goriainov, S. V., Chistyakov, V. V., Tiulina, V. V., Gancharova, O. S., Baksheeva, V. E., Zamyatnin, A. A., Philippov, P. P., Sergeeva, M. G., Senin, I. I., Zernii, E. Yu
• Format: Journal Article
• Language: English
• Published: Moscow Pleiades Publishing 01.04.2020; Springer Nature B.V
• Subjects: Anesthesia; Anti-inflammatory agents; Antioxidants; Biomedical and Life Sciences; Cell Biology; Cornea; Cytochromes; Derivatives; Inflammation; Inflammatory response; Inhibitors; Life Sciences; Lipoxygenase; Metabolites; Oxidation; Oxidative stress; Prostaglandin endoperoxide synthase; Spectrometry; dry eye syndrome; inflammation; tear fluid; oxylipins; corneal erosion; general anesthesia; oxidative stress
• ISSN: 1990-7478; 1990-7494
• DOI: 10.1134/S1990747819060047

Using the previously developed rabbit model of perioperative dry eye syndrome (PDES) and quantitative mass spectrometric technique it is shown that the development of corneal erosion under conditions of general anesthesia is associated with changes in the content of inflammatory metabolites, namely, derivatives of linoleic (LA), alpha-linolenic (ALA), and arachidonic (AA) acids in tear fluid. The increase in the content of the metabolites of LA and ALA is found to be the most significant, while the content of AA derivatives (with the exception of 12-HETE) remains almost unchanged, indicating the key roles of the LA and ALA cascades in the inflammatory response in PDES. The increase in the concentration of oxylipins that can be formed by nonenzymatic oxidation of LA (9-KODE) or its processing by cytochromes (12,13-EpOME) under oxidative conditions indicates a significant contribution of oxidative stress to the development of PDES. The majority of metabolites of LA (13-HODE and 9-HODE), ALA (9-HOTrE and 13-HOTrE) and AA (12-HETE), the tear content of which was changed in PDES, are generated by the enzymes of lipoxygenase family. By contrast, the concentration of cyclooxygenase products does not exhibit any significant fluctuations. These data suggest a low therapeutic potential of cyclooxygenase inhibitors (such as nonsteroidal anti-inflammatory drugs) and a high therapeutic potential of antioxidants and lipoxygenase inhibitors in PDES, which should be taken into account upon developing a complex therapy for this disease.