A novel rat model of ocular hypertension by a single intracameral injection of cross‐linked hyaluronic acid hydrogel (Healaflow®). Issue 5 (9th June 2020)

• Record Type: Journal Article
• Authors: Liu, Ying; Wang, Jichen; Jin, Xin; Xin, Zhiyuan; Wu, Xing; Tong, Xu; Tao, Ye; Wang, Dajiang
• Is Part Of: Basic & clinical pharmacology & toxicology. Volume 127:Issue 5(2020)
• Page Start: 361
• Page End: 370
• Publication Date: 2020-06-09
• Subjects: glaucoma -- Healaflow® -- intraocular pressure -- ocular hypertension -- retinal ganglion cells; Pharmacology -- Periodicals; Toxicology -- Periodicals; Pharmacology -- Periodicals; Toxicology -- Periodicals; Pharmacology, Clinical -- Periodicals; Computer network resources; Electronic journals; 615.1
• DOI: 10.1111/bcpt.13430
• Languages: English
• ISSNs: 1742-7835

Abstract

Abstract: To create a novel animal model of ocular hypertension via the intracameral injection of Healaflow. Unilateral chronic ocular hypertension model of rats was created by the intracameral injection of 3 μL Healaflow. The IOP of subjects was monitored. Dynamic morphological changes were evaluated by fundus imaging, OCT and histological examination. Visual function changes were measured by electroretinography and flash visual‐evoked potentials. 24 and 72 hours after injection, the retinal tissue was collected for transcriptome analysis. The expression levels of related genes and proteins were further evaluated by qRT‐PCR and Western blotting. The IOP peaked within 1 day after a single intracameral injection of Healaflow and then decreased gradually within 4 weeks. Furthermore, the persistently degenerating retinal ganglion cells occurred within 4 weeks. The visual function of these rats was also impaired. The results of transcriptome analyses, qRT‐PCR and Western blotting showed that the expression levels of B2m, Ikzf1 and Stat3 were up‐regulated, while the expression levels of Six3 and Prss56 were down‐regulated in the retinal tissues. Intracameral injection of Healaflow is an effective approach to induce glaucomatous neurodegeneration in rats. Six3 and Prss56 may be involved in the pathogenesis of progressive glaucomatous damage.