Rodent Models of Glaucoma: Pathogenic Mechanisms, Phenotyping Strategies, and Translational Relevance.

Glaucoma comprises a heterogeneous group of optic neuropathies characterized by progressive degeneration of retinal ganglion cells (RGCs) and their axons. Rodent models have been widely used to investigate disease mechanisms, identify neuroprotective targets and evaluate emerging therapeutic strategies because they are cost-effective, genetically tractable and experimentally controllable. However, mice and rats differ substantially from humans in anterior-segment anatomy, trabecular meshwork architecture, Schlemm's canal development, lamina cribrosa structure, retinal ganglion cell composition and optic nerve head vascular supply. These interspecies differences influence model construction, phenotypic interpretation and the translational value of preclinical findings. This narrative review summarizes key anatomical differences between rodent and human eyes and discusses major categories of rodent glaucoma models, including intraocular pressure (IOP)-dependent models, IOP-independent models, immune-mediated and multifactorial models, and spontaneous or genetically engineered models. We emphasize that no single rodent model can fully reproduce the chronic, multifactorial, and regionally selective nature of human glaucoma. Instead, model selection should be driven by the specific scientific question, disease subtype, observation window, and translational goal. IOP-dependent models are particularly useful for investigating pressure-induced RGC degeneration and optic nerve injury, while selected models also reproduce aspects of aqueous outflow dysfunction, linking anterior-segment abnormalities with posterior-segment neurodegeneration. IOP-independent and genetic models, by contrast, are ideal for studying normal-tension glaucoma, neurodegeneration, neuroinflammation, metabolic stress, and gene-specific mechanisms. Future efforts should prioritize standardized phenotypic evaluation, multimodal imaging and multi-omics integration to improve the reliability and translational relevance of findings from rigorously validated rodent models.