A total of 30 white Dutch rabbits, aged between 6 and 18 months, with a mean weight of 2200 ± 500 g, were selected for the study. In the initial screening, the animals were examined carefully and any that had symptoms of eye problems, such as; redness, inflammation, chemosis, conjunctivitis, mucopurulent discharge, or any other ophthalmic or general clinical disease such as any evidence of upper respiratory tract infection, were excluded from the study.
Experiments were conducted in accordance with the ARVO Statement for the Use of Animals in Ophthalmic and Vision Research and the Guiding Principles in the Care and Use of Animals. The rabbits were divided into three groups. All of the animals were kept in a room containing only rabbits. Two rabbits were each housed in one cage and there was no direct connection between the cages. They were fed daily with commercial pet food, which was placed in front of the cages. The rooms were appropriately ventilated. Prior to any intervention, animals were anesthetized with ketamine 50 mg/kg to provide appropriate conditions.
Conjunctival and eyelid swabs were collected from the right eye of the rabbits at the beginning of the study, before the intervention. Sterile cotton swabs were moistened with sterile normal saline which werethen wiped along the lower fornix of the right eye by everting the eyelid. During sampling, any contact of the swabs with eyelashes, eyelid skin or lacrimal punctum was avoided. A separate sterile swab was used for each eyelid specimen. Then the swabs were immediately streaked onto a blood agar plate. The plates were incubated at 37ºC for 24 hours. After 24 hours, the cultures were examined. If there was not enough growth of the colonies, they were reincubated for a further 24 hours. After 48 hours, the isolated colonies were identified by cultural characteristics and gram staining. By performing this phase, before instillation of the onion juice, we were able to find out more about the most common organisms that frequently inhabit the conjunctiva and eyelid of healthy rabbits. These results were then used as control data to compare with the results obtained after onion juice administration.
A standard fluorescein strip was applied to the eye for cornea and conjunctival staining. The areas of positive staining showed epithelial changes. Any positive finding was recorded on a data sheet. According to previous reports, red onion has the highest content of flavonoids among other kinds of onions (
12). Therefore, fresh red onion was purchased from local markets. The onion juice was prepared fresh each time before instillation, by peeling and grinding the onion for about 10–15 minutes using a blender. Then the ground material was filtered by Nalgene sterile bottle filters, and the crude extract centrifuged (3000 rpm, at 4°C) until a relatively clear supernatant liquid was obtained. The onion juice was then poured into a sterile eye dropper.
Twice daily, the juice was instilled into the right eye of the animals. Group 1 received onion juice eye drops for one week, Group 2 for one month, and Group 3 were exposed to the juice for two months. At the end of the study, a microbiological assessment of each eye’s normal flora was conducted using the same method described in the preliminary phase and a pathological specimen was obtained from the lower conjunctival fornix of the right eye in the form of a tissue strip (about 5-6 mm2). They were kept in formalin as a transport medium.
After sample processing, very fine sectional specimens embedded in paraffin were cut and then stained with hematoxylin and eosin (H&E) to determine the presence or absence of; inflammation, metaplasia, dysplasia and fibrosis. The pathologist, who performed all of the histological examinations, was blinded to the groups. Chi-squared tests were used to analyze the data and compare the results between the three studied groups. A P value less than 0.05 was considered as significant.