Can metformin modulate the retinal degenerative changes in a rat model of retinitis pigmentosa?

• Published in: Tissue & cell Vol. 76; p. 101786
• Main Authors: Eltony, Sohair A., Mohaseb, Heba S., Ahmed, Amel A., Sayed, Manal M.
• Format: Journal Article
• Language: English
• Published: Scotland Elsevier Ltd 01.06.2022; Elsevier Science Ltd
• Subjects: Acidic oxides; Animal models; Apoptosis; Blood; Blood vessels; Capillaries; Caspase-3; Cell death; Degeneration; Electron microscopy; Ethyl nitrosourea; Glial fibrillary acidic protein; Macrophages; Markers; Metformin; Microglia; Morphology; Mueller cells; Neuroprotection; Nitric-oxide synthase; Oxidative stress; Photoreceptor degeneration; Photoreceptors; Retina; Retinal degeneration; Retinitis; Retinitis pigmentosa; Rodents; Subgroups; Retina; Metformin; Retinitis pigmentosa; Photoreceptor degeneration
• ISSN: 0040-8166; 1532-3072
• DOI: 10.1016/j.tice.2022.101786

Retinitis pigmentosa (RP) affects over a million people worldwide, characterized by photoreceptor cell death, progressive retinal degeneration, and visual loss. Metformin is demonstrated as a potential therapeutic approach for preventing light-induced retinal degeneration by decreasing apoptosis and oxidative stress. This work aimed to investigate the effect of metformin on the retina of the N-Ethyl-N-nitrosourea (ENU) induced rat model of RP. Eighteen adult male Wistar rats were divided into two groups. Group I: normal vehicle control (N = 6). Group II: ENU-induced photoreceptor degeneration (N = 12) received a single intraperitoneal injection of ENU at a 600 mg/kg dose. Rats in group II were equally divided into two subgroups: IIa: photoreceptor degeneration-induced group and IIb: metformin-treated group (200 mg/kg) for seven days. Specimens from the retina were processed for light and electron microscopy. In ENU treated group, the retina revealed vacuolations and morphological changes in the glia (Müller cells and microglia) and blood capillaries. Increasing caspase-3 (apoptotic marker), iNOS (oxidative stress marker), CD68 (macrophage marker) and glial fibrillary acidic protein (GFAP) expression were detected. In the metformin-treated group, the retinal vacuolations reduced with the morphological improvement in the glia and blood capillaries. Caspase-3, iNOS, CD68, and GFAP expression decreased. Metformin was found to have a neuroprotective effect on the retina in ENU induced rat model of RP •Retinitis pigmentosa (RP) is a cause of inherited blindness characterized by photoreceptor cell death.•Metformin is demonstrated to prevent light-induced retinal degeneration by decreasing apoptosis and oxidative stress.•This study investigated the effect of metformin on the retina of N-Ethyl-N-nitrosourea (ENU) induced rat model of RP.•Metformin suppressed microglia and Müller cells activation and improved the changes in the retinal blood capillaries.•Metformin was found to have a neuroprotective effect on the retina in ENU induced rat model of RP.