Impaired spatial navigation and age‐dependent hippocampal synaptic dysfunction are associated with chronic inflammatory response in db/db mice

• Published in: The European journal of neuroscience Vol. 56; no. 11; pp. 6003 - 6021
• Main Authors: Al‐Onaizi, Mohammed, Al‐Sarraf, Ahmad, Braysh, Kawthar, Kazem, Fatema, Al‐Hussaini, Heba, Rao, Muddanna, Kilarkaje, Narayana, ElAli, Ayman
• Format: Journal Article
• Language: English
• Published: France Wiley Subscription Services, Inc 01-12-2022
• Subjects: Aging; Alzheimer Disease - metabolism; Alzheimer's disease; Animals; Cognitive ability; Cytokines; Cytokines - metabolism; Dentate gyrus; diabetes mellitus; Diabetes mellitus (non-insulin dependent); Diabetes Mellitus, Type 2; Disease Models, Animal; Hippocampus; Hippocampus - metabolism; Inflammation; Inflammation - metabolism; memory; Mice; Navigation behavior; Neurodegenerative diseases; neuroinflammation; Postsynaptic density; Postsynaptic density proteins; Proteins; Spatial Navigation; Synaptophysin; Synaptophysin - metabolism; cytokines; diabetes mellitus; memory; hippocampus; neuroinflammation; Alzheimer's disease
• ISSN: 0953-816X; 1460-9568
• DOI: 10.1111/ejn.15835

Type 2 diabetes mellitus (T2DM) increases the risk of developing Alzheimer's disease (AD), which has been proposed to be driven by an abnormal neuroinflammatory response affecting cognitive function. However, the impact of T2DM on hippocampal function and synaptic integrity during aging has not been investigated. Here, we investigated the effects of aging in T2DM on AD‐like pathology using the leptin receptor‐deficient db/db mouse model of T2DM. Our results indicate that adult T2DM mice exhibited impaired spatial acquisition in the Morris water maze (MWM). Morphological analysis showed an age‐dependent neuronal loss in the dentate gyrus. We found that astrocyte density was significantly decreased in all regions of the hippocampus in T2DM mice. Our analysis showed that microglial activation was increased in the CA3 and the dentate gyrus of the hippocampus in an age‐dependent manner in T2DM mice. However, the expression of presynaptic marker protein (synaptophysin) and the postsynaptic marker protein [postsynaptic density protein 95 (PSD95)] was unchanged in the hippocampus of adult T2DM mice. Interestingly, synaptophysin and PSD95 expression significantly decreased in the hippocampus of aged T2DM mice, suggesting an impaired hippocampal synaptic integrity. Cytokine profiling analysis displayed a robust pro‐inflammatory cytokine profile in the hippocampus of aged T2DM mice compared with the younger cohort, outlining the role of aging in exacerbating the neuroinflammatory profile in the diabetic state. Our results suggest that T2DM impairs cognitive function by promoting neuronal loss in the dentate gyrus and triggering an age‐dependent deterioration in hippocampal synaptic integrity, associated with an aberrant neuroinflammatory response.