Metabolic effect of the retina in a murine model of AD

Aims/Purpose: The aim of the study is to evaluate energy metabolism and retinal tissue survival in retinal explants in a murine model of AD (TgSwDI) during aging. Methods: The 7-, 12- and 24-month-old TgSwDI mouse model was compared with age-matched wild-type (WT) mice. Characterization of the mouse model was assessed by A? plaques staining. Cell viability was evaluated by lactate dehydrogenase (LDH) assay of retinal explants at 4 and 24?h of incubation with culture media. Retinal ganglion cell (RGC) survival was quantified by RBPMS staining in 7-month-old mice. Glucose metabolism was analysed by gas chromatography mass spectrometry (GC?MS) using uniformly labelled glucose by incubating whole retinas for 30?min with glucose in 7-month-old mice. And lactate, produced by glycolysis, was evaluated by the lactate assay in 7-month-old mice. Results: The presence of A? plaques and vascularization was detected in the retinas of TgSwDI mice, whereas they were not found in the retinas of control mice. At 7?months, the viability of retinal explants was reduced in the TgSwDI model compared to the age-matched WT model using the LDH assay. Compared to controls, RGC survival in the TgSwDI model tended to decrease. We performed GC?MS to evaluate glucose metabolism and observed no difference between the TgSwDI and WT groups. Lactate production showed no significant differences between the groups. Conclusions: The presence of A? plaques was detected in the retinas of the TgSwDI model, indicating that it is a good model for studying the retina in AD. Retinal tissue viability was altered at different ages in the TgSwDI model, and RGC survival was also reduced in the AD model, substantiating that AD affect the retina. We did not detect any differences between WT and TgSwDI groups in energy metabolism, implying that alterations in retinal tissue and cell survival may be related to other pathways. Further studies are needed to explore this, ultimately providing novel insight to address visual function affected by AD.