| Literature DB >> 34073191 |
Marie Claes1, Joana R F Santos1,2,3,4, Luca Masin1, Lien Cools1, Benjamin M Davis5,6, Lutgarde Arckens1, Karl Farrow1,2,3,4, Lies De Groef1, Lieve Moons1.
Abstract
Despite being one of the most studied eye diseases, clinical translation of glaucoma research is hampered, at least in part, by the lack of validated preclinical models and readouts. The most popular experimental glaucoma model is the murine microbead occlusion model, yet the observed mild phenotype, mixed success rate, and weak reproducibility urge for an expansion of available readout tools. For this purpose, we evaluated various measures that reflect early onset glaucomatous changes in the murine microbead occlusion model. Anterior chamber depth measurements and scotopic threshold response recordings were identified as an outstanding set of tools to assess the model's success rate and to chart glaucomatous damage (or neuroprotection in future studies), respectively. Both are easy-to-measure, in vivo tools with a fast acquisition time and high translatability to the clinic and can be used, whenever judged beneficial, in combination with the more conventional measures in present-day glaucoma research (i.e., intraocular pressure measurements and post-mortem histological analyses). Furthermore, we highlighted the use of dendritic arbor analysis as an alternative histological readout for retinal ganglion cell density counts.Entities:
Keywords: anterior chamber depth; dendritic retraction; electroretinography; glaucoma; microbead occlusion model; neurodegeneration; ocular hypertension; optical coherence tomography; retinal ganglion cells; scotopic threshold response
Year: 2021 PMID: 34073191 DOI: 10.3390/ijms22115633
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923