Journal of Cellular and Molecular Medicine · 2008 · 123 citations · 37 references
Life SciencesNeurobiologyNutritional SciencesAgingCellular NeuroscienceMitochondrial BiologyAging PhysiologyMitochondrial DysfunctionMitochondrial FunctionMitochondrial StructureMitochondrial UltrastructureNeuroprotectionCristae MorphologyDietary Supplementation EffectsMitochondrial Dysfunction In AgingMitochondrial Integrity ControlMitochondrial Integrity PreservationQuantitative MicroscopyRegulation Of Mitochondrial IntegrityVessel Wall Structure
Brain function declines with age and is associated with diminishing mitochondrial integrity. The neuronal mitochondrial ultrastructural changes of young (4 months) and old (21 months) F344 rats supplemented with two mitochondrial metabolites, acetyl-L-carnitine (ALCAR, 0.2%[wt/vol] in the drinking water) and R-alpha-lipoic acid (LA, 0.1%[wt/wt] in the chow), were analysed using qualitative and quantitative electron microscopy techniques. Two independent morphologists blinded to sample identity examined and scored all electron micrographs. Mitochondria were examined in each micrograph, and each structure was scored according to the degree of injury. Controls displayed an age-associated significant decrease in the number of intact mitochondria (P = 0.026) as well as an increase in mitochondria with broken cristae (P < 0.001) in the hippocampus as demonstrated by electron microscopic observations. Neuronal mitochondrial damage was associated with damage in vessel wall cells, especially vascular endothelial cells. Dietary supplementation of young and aged animals increased the proliferation of intact mitochondria and reduced the density of mitochondria associated with vacuoles and lipofuscin. Feeding old rats ALCAR and LA significantly reduced the number of severely damaged mitochondria (P = 0.02) and increased the number of intact mitochondria (P < 0.001) in the hippocampus. These results suggest that feeding ALCAR with LA may ameliorate age-associated mitochondrial ultrastructural decay and are consistent with previous studies showing improved brain function.
37
Extension of Murine Life Span by Overexpression of Catalase Targeted to Mitochondria
Samuel E. Schriner, Nancy J. Linford, George M. Martin et al. · Science · 2005 · 1.7K citations
Life Sciences, Biochemistry, Biology +17
Mitochondrial Abnormalities in Alzheimer's Disease
Keisuke Hirai, Gjumrakch Aliev, Akihiko Nunomura et al. · Journal of Neuroscience · 2001 · 1.4K citations · Full text
ABAD Directly Links Aß to Mitochondrial Toxicity in Alzheimer's Disease
Joyce W. Lustbader, Maurizio Cirilli, Chang Lin et al. · Science · 2004 · 1.3K citations
Jiankang Liu, Elizabeth Head, Afshin Gharib et al. · Proceedings of the National Academy of Sciences · 2002 · 507 citations · Full text