Low Intraocular Pressure Induces Fibrotic Changes in the Trabecular Meshwork and Schlemm's Canal of Sprague Dawley Rats

• Published in: Translational vision science & technology Vol. 13; no. 10; p. 10
• Main Authors: Xu, Lijuan, Zhao, Yin, Zhang, Xinyao, Gang, Xiaorui, Han, Jialing, Zhou, Tao, Qi, Binyan, Song, Shuning, Ren, Ruiyi, Liang, Yuanbo
• Format: Journal Article
• Language: English
• Published: United States 01.10.2024
• Subjects: Animals; Apoptosis; Aqueous Humor - metabolism; Disease Models, Animal; Fibrosis - pathology; Intraocular Pressure - physiology; Kruppel-Like Factor 4; Male; Rats; Rats, Sprague-Dawley; Schlemm's Canal; Trabecular Meshwork - metabolism; Trabecular Meshwork - pathology
• ISSN: 2164-2591; 2164-2591
• DOI: 10.1167/tvst.13.10.10

Continuous artificial aqueous humor drainage in the eyes of patients with glaucoma undergoing trabeculectomy likely exerts abnormal shear stress. However, it remains unknown how changes in intraocular pressure (IOP) can affect aqueous humor outflow (AHO). Here, we induced and maintained low intraocular pressure (L-IOP) in healthy Sprague Dawley (SD) rats by puncturing their eyes using a tube (200-µm diameter) for 2 weeks. After the rats were euthanized, their eyes were removed, fixed, embedded, stained, and scanned to analyze the physiological and pathological changes in the trabecular meshwork (TM) and Schlemm's canal (SC). We measured SC parameters using ImageJ software and assessed the expression of various markers related to flow shear stress (KLF4), fibrosis (TGF-β1, TGF-β2, α-SMA, pSmad1/5, pSmad2/3, and fibronectin), cytoskeleton (integrin β1 and F-actin), diastolic function (nitric oxide synthase and endothelial nitric oxide synthase [eNOS]), apoptosis (cleaved caspase-3), and proliferation (Ki-67) using immunofluorescence or immunohistochemistry. L-IOP eyes showed a larger SC area, higher eNOS expression, and lower KLF4 and F-actin expression in the TM and SC (both P < 0.05) than control eyes. The aqueous humor of L-IOP eyes had a higher abundance of fibrotic proteins and apoptotic cells than that of control eyes, with significantly higher TGF-β1, α-SMA, fibronectin, and cleaved caspase-3 expression (all P < 0.05). In conclusion, a persistence of L-IOP for 2 weeks may contribute to fibrosis in the TM and SC and might be detrimental to conventional AHO in SD rat eyes. Clinicians should consider that aberrant shear force induced by aqueous humor fluctuation may damage AHO outflow channel when treating patients.