Moreira_2012_J.Alzheimers.Dis_32_495

There is increasing evidence that hypercholesterolemia during midlife may represent a predictor of subsequent mild cognitive impairments and dementia decades later However the exact mechanism underlying this phenomenon remains unknown since plasmatic cholesterol is not able to cross the blood-brain barrier In the present study we evaluated the hypothesis that cognitive impairments triggered by hypercholesterolemia during aging may be related to brain oxidative stress and altered brain acetylcholinesterase AChE activity We also performed a neuropathological investigation in order to analyze whether the cognitive impairments may be associated with stroke-related features To address these questions we used three and fourteen-month-old low-density lipoprotein receptor-deficient mice LDLr The current findings provide new evidence that aged LDLr mice exposed to over three-fold cholesterol levels from early life show working spatial reference and procedural memory impairments without alterations in motor function Antioxidant imbalance and oxidative damage were evidenced by a marked increase in lipid peroxidation thiobarbituric acid reactive substances levels and glutathione metabolism increase in glutathione levels glutathione reductase and glutathione peroxidase activities together with a significant increase in the AChE activity in the prefrontal cortex of aged hypercholesterolemic LDLr mice Notably hypercholesterolemia was not related to brain infarcts and neurodegeneration in mice independent of their age These observations provide new evidence that hypercholesterolemia during aging triggers cognitive impairments on different types of learning and memory accompanied by antioxidant imbalance oxidative damage and alterations of cholinergic signaling in brain areas associated with learning and memory processes particularly in the prefrontal cortex.