Differential central pathology and cognitive impairment in pre-diabetic and diabetic mice

Juan Jose Ramos-Rodriguez, Oscar Ortiz, Margarita Jimenez-Palomares, Kevin R Kay, Esther Berrocoso, Maria Isabel Murillo-Carretero, German Perdomo, Tara Spires-Jones, Irene Cozar-Castellano, Alfonso Maria Lechuga-Sancho, Monica Garcia-Alloza

Research output: Contribution to journalArticlepeer-review


Although age remains the main risk factor to suffer Alzheimer's disease (AD) and vascular dementia (VD), type 2 diabetes (T2D) has turned up as a relevant risk factor for dementia. However, the ultimate underlying mechanisms for this association remain unclear. In the present study we analyzed central nervous system (CNS) morphological and functional consequences of long-term insulin resistance and T2D in db/db mice (leptin receptor KO mice). We also included C57Bl6 mice fed with high fat diet (HFD) and a third group of C57Bl6 streptozotocin (STZ) treated mice. Db/db mice exhibited pathological characteristics that mimic both AD and VD, including age dependent cognitive deterioration, brain atrophy, increased spontaneous hemorrhages and tau phosphorylation, affecting the cortex preferentially. A similar profile was observed in STZ-induced diabetic mice. Moreover metabolic parameters, such as body weight, glucose and insulin levels are good predictors of many of these alterations in db/db mice. In addition, in HFD-induced hyperinsulinemia in C57Bl6 mice, we only observed mild CNS alterations, suggesting that central nervous system dysfunction is associated with well established T2D. Altogether our results suggest that T2D may promote many of the pathological and behavioral alterations observed in dementia, supporting that interventions devoted to control glucose homeostasis could improve dementia progress and prognosis.
Original languageEnglish
Pages (from-to)2462-75
Number of pages14
Issue number11
Publication statusPublished - Nov 2013


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