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Cornea

Protective Effect of Allyl Isothiocyanate in an Experimentally Induced Rat Model for Dry Eye Syndrome

ORCID Icon, ORCID Icon, ORCID Icon, , , , & ORCID Icon show all
Pages 704-714 | Received 24 May 2021, Accepted 09 Dec 2021, Published online: 21 Mar 2022
 

Abstract

Purpose

Growing evidence emphasizes the role of inflammation and oxidative stress in the pathogenesis of Dry Eye Syndrome (DES). Concordantly, the importance of agents targeting the inflammatory cascade and oxidative stress in the treatment is also progressively increasing. Herein, the study has investigated the protective effects and underlying mechanism of allyl isothiocyanate (AITC) on the ocular surface in a benzalkonium chloride (BAC)-induced dry eye rat model.

Methods

A total of twenty-one Wistar albino rats were used to form the following three groups: Control, BAC, BAC + AITC. DES was established by topical application of BAC (four times daily for two weeks) in two groups, of which one group was treated with AITC (10 mg/kg BW daily oral dosage) for four weeks. Rats were monitored by dry eye diagnostic tests during the study period, and eventually, corneal tissues were used to evaluate for histopathologic analyzes and inflammatory and oxidative status.

Results

A significant improvement was observed in various histopathologic and ophthalmologic findings, including tear volume, tear film integrity, ocular surface damage, ocular inflammatory signs, corneal thickness, and edema through AITC supplementation. AITC prominently balanced the inflammatory status and oxidative stress by lowering key proinflammatory mediators (NF-κB, TNF-α, IL-1β, IL-6, and IL-8) and increasing the activities of antioxidant enzymes (SOD, GSH-Px). Also, levels of protective tear proteins, including Muc1, Muc4, and Muc5 were recovered with AITC supplementation.

Conclusion

AITC alleviates clinical and histopathologic signs related to DES. Antioxidative and anti-inflammatory properties of AITC play a significant role in the mechanism of action.

Acknowledgments

The authors thank OmniActive Health Technologies Inc. (NJ, USA) and the Turkish Academy of Sciences (K.S.) for supporting the project.

Disclosure statement

AM and MP are employees of OmniActive Health Technologies. The other authors confirm that they have no conflicts of interest with respect to the work described in this manuscript.

Additional information

Funding

This work was supported by OmniActive Health Technologies (Mumbai, India) and the Turkish Academy of Sciences (in part, K.S.).

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