Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/114767
Title: Normative mice retinal thickness: 16-month longitudinal characterization of wild-type mice and changes in a model of Alzheimer's disease
Authors: Batista, Ana 
Guimarães, Pedro 
Martins, João 
Moreira, Paula I. 
Ambrósio, António Francisco 
Castelo-Branco, Miguel 
Serranho, Pedro 
Bernardes, Rui 
Keywords: optical coherence tomography; retinal thickness; normative data; Alzheimer’s disease; 3×Tg-AD animal model
Issue Date: 2023
Publisher: Frontiers Media S.A.
Project: PTDC/EMD-EMD/28039/2017 
UIDB/04950/2020 
Pest-UID/NEU/04539/2019 
POCI-01-0145-FEDER-028039 
Serial title, monograph or event: Frontiers in Aging Neuroscience
Volume: 15
Abstract: Animal models of disease are paramount to understand retinal development, the pathophysiology of eye diseases, and to study neurodegeneration using optical coherence tomography (OCT) data. In this study, we present a comprehensive normative database of retinal thickness in C57BL6/129S mice using spectral-domain OCT data. The database covers a longitudinal period of 16 months, from 1 to 16 months of age, and provides valuable insights into retinal development and changes over time. Our findings reveal that total retinal thickness decreases with age, while the thickness of individual retinal layers and layer aggregates changes in different ways. For example, the outer plexiform layer (OPL), photoreceptor inner segments (ILS), and retinal pigment epithelium (RPE) thickened over time, whereas other retinal layers and layer aggregates became thinner. Additionally, we compare the retinal thickness of wild-type (WT) mice with an animal model of Alzheimer's disease (3 × Tg-AD) and show that the transgenic mice exhibit a decrease in total retinal thickness compared to age-matched WT mice, with statistically significant differences observed at all evaluated ages. This normative database of retinal thickness in mice will serve as a reference for future studies on retinal changes in neurodegenerative and eye diseases and will further our understanding of the pathophysiology of these conditions.
URI: https://hdl.handle.net/10316/114767
ISSN: 1663-4365
DOI: 10.3389/fnagi.2023.1161847
Rights: openAccess
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
I&D ICBR - Artigos em Revistas Internacionais
I&D ICNAS - Artigos em Revistas Internacionais
I&D CIBIT - Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais

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