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Dry eye syndrome model established in rabbits via mitomycin C injection in the lacrimal gland
PURPOSE: To develop a new dry eye syndrome (DES) animal model by injecting mitomycin C (MMC) into the lacrimal glands (LGs) of rabbits evaluated by clinical examinations. MATERIALS AND METHODS: A volume of 0.1 mL of MMC solution was injected in the LG and the infraorbital lobe of the accessory LG of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220434/ https://www.ncbi.nlm.nih.gov/pubmed/37252170 http://dx.doi.org/10.4103/tjo.tjo_11_22 |
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author | Lin, I-Chan Wang, Yu-Chio Chen, Yi-Zhou Tang, Yu-Jun Chen, Ko-Hua Tseng, Ching-Li |
author_facet | Lin, I-Chan Wang, Yu-Chio Chen, Yi-Zhou Tang, Yu-Jun Chen, Ko-Hua Tseng, Ching-Li |
author_sort | Lin, I-Chan |
collection | PubMed |
description | PURPOSE: To develop a new dry eye syndrome (DES) animal model by injecting mitomycin C (MMC) into the lacrimal glands (LGs) of rabbits evaluated by clinical examinations. MATERIALS AND METHODS: A volume of 0.1 mL of MMC solution was injected in the LG and the infraorbital lobe of the accessory LG of rabbits for DES induction. Twenty male rabbits were separated into three groups, the control group, and different concentration of MMC, (MMC 0.25: 0.25 mg/mL or MMC 0.50: 0.5 mg/mL) were tested. Both MMC-treated groups received MMC twice injection on day 0 and day 7. Assessment of DES included changes in tear production (Schirmer's test), fluorescein staining pattern, conjunctival impression cytology, and corneal histological examination. RESULTS: After MMC injection, no obvious changes in the rabbit's eyes were noted by slit-lamp examination. Both the MMC 0.25 and the MMC 0.5 groups revealed decreased tear secretion after injection, and the MMC 0.25 group showed a continuous decrease in tear secretion up to 14 days. Fluorescent staining showed punctate keratopathy in both MMC-treated groups. In addition, both MMC-treated groups demonstrated decreased numbers of conjunctival goblet cells after injection. CONCLUSION: This model induced decreased tear production, punctate keratopathy, and decreased numbers of goblet cells, which are consistent with the current understanding of DES. Therefore, injecting MMC (0.25 mg/mL) into the LGs is an easy and reliable method to establish a rabbit DES model which can apply in new drug screening. |
format | Online Article Text |
id | pubmed-10220434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-102204342023-05-28 Dry eye syndrome model established in rabbits via mitomycin C injection in the lacrimal gland Lin, I-Chan Wang, Yu-Chio Chen, Yi-Zhou Tang, Yu-Jun Chen, Ko-Hua Tseng, Ching-Li Taiwan J Ophthalmol Original Article PURPOSE: To develop a new dry eye syndrome (DES) animal model by injecting mitomycin C (MMC) into the lacrimal glands (LGs) of rabbits evaluated by clinical examinations. MATERIALS AND METHODS: A volume of 0.1 mL of MMC solution was injected in the LG and the infraorbital lobe of the accessory LG of rabbits for DES induction. Twenty male rabbits were separated into three groups, the control group, and different concentration of MMC, (MMC 0.25: 0.25 mg/mL or MMC 0.50: 0.5 mg/mL) were tested. Both MMC-treated groups received MMC twice injection on day 0 and day 7. Assessment of DES included changes in tear production (Schirmer's test), fluorescein staining pattern, conjunctival impression cytology, and corneal histological examination. RESULTS: After MMC injection, no obvious changes in the rabbit's eyes were noted by slit-lamp examination. Both the MMC 0.25 and the MMC 0.5 groups revealed decreased tear secretion after injection, and the MMC 0.25 group showed a continuous decrease in tear secretion up to 14 days. Fluorescent staining showed punctate keratopathy in both MMC-treated groups. In addition, both MMC-treated groups demonstrated decreased numbers of conjunctival goblet cells after injection. CONCLUSION: This model induced decreased tear production, punctate keratopathy, and decreased numbers of goblet cells, which are consistent with the current understanding of DES. Therefore, injecting MMC (0.25 mg/mL) into the LGs is an easy and reliable method to establish a rabbit DES model which can apply in new drug screening. Wolters Kluwer - Medknow 2022-05-04 /pmc/articles/PMC10220434/ /pubmed/37252170 http://dx.doi.org/10.4103/tjo.tjo_11_22 Text en Copyright: © 2022 Taiwan Journal of Ophthalmology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Lin, I-Chan Wang, Yu-Chio Chen, Yi-Zhou Tang, Yu-Jun Chen, Ko-Hua Tseng, Ching-Li Dry eye syndrome model established in rabbits via mitomycin C injection in the lacrimal gland |
title | Dry eye syndrome model established in rabbits via mitomycin C injection in the lacrimal gland |
title_full | Dry eye syndrome model established in rabbits via mitomycin C injection in the lacrimal gland |
title_fullStr | Dry eye syndrome model established in rabbits via mitomycin C injection in the lacrimal gland |
title_full_unstemmed | Dry eye syndrome model established in rabbits via mitomycin C injection in the lacrimal gland |
title_short | Dry eye syndrome model established in rabbits via mitomycin C injection in the lacrimal gland |
title_sort | dry eye syndrome model established in rabbits via mitomycin c injection in the lacrimal gland |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10220434/ https://www.ncbi.nlm.nih.gov/pubmed/37252170 http://dx.doi.org/10.4103/tjo.tjo_11_22 |
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