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Difference between revisions of "Dias 2016 Neurobiol Aging"

From Bioblast
 
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|title=Dias C, Lourenço CF, Ferreiro E, Barbosa RM, Laranjinha J, Ledo A (2016) Age-dependent changes in the glutamate-nitric oxide pathway in the hippocampus of the triple transgenic model of Alzheimer's disease: implications for neurometabolic regulation. Neurobiol Aging 46:84-95.
|title=Dias C, Lourenço CF, Ferreiro E, Barbosa RM, Laranjinha J, Ledo A (2016) Age-dependent changes in the glutamate-nitric oxide pathway in the hippocampus of the triple transgenic model of Alzheimer's disease: implications for neurometabolic regulation. Neurobiol Aging 46:84-95.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/27460153 PMID: 27460153]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/27460153 PMID: 27460153]
|authors=Dias C, Lourenco CF, Ferreiro E, Barbosa RM, Laranjinha J, Ledo A
|authors=Dias C, Lourenco CF, Ferreiro E, Barbosa RM, Laranjinha J, Ledo AM
|year=2016
|year=2016
|journal=Neurobiol Aging
|journal=Neurobiol Aging

Latest revision as of 17:05, 12 July 2019

Publications in the MiPMap
Dias C, Lourenço CF, Ferreiro E, Barbosa RM, Laranjinha J, Ledo A (2016) Age-dependent changes in the glutamate-nitric oxide pathway in the hippocampus of the triple transgenic model of Alzheimer's disease: implications for neurometabolic regulation. Neurobiol Aging 46:84-95.

» PMID: 27460153

Dias C, Lourenco CF, Ferreiro E, Barbosa RM, Laranjinha J, Ledo AM (2016) Neurobiol Aging

Abstract: Age-dependent changes in nitric oxide ((•)NO) concentration dynamics may play a significant role in both decaying synaptic and metabolic functions in Alzheimer's disease (AD). This neuromodulator acts presynaptically to increase vesicle release and glutamatergic transmission and also regulates mitochondrial function. Under conditions of altered intracellular redox environment, (•)NO may react and produce reactive species such as peroxynitrite. Using the triple transgenic mouse model of AD (3xTgAD), we investigated age-dependent changes in the glutamate-(•)NO axis in the hippocampus. Direct measurement of (•)NO concentration dynamics revealed a significant increase in N-methyl-D-aspartate type receptor-evoked peak (•)NO in the 3xTgAD model at an early age. Aging produced a decrease in peak (•)NO accompanied by significant decrease in production and decay rates in the transgenic model. Evaluation of energy metabolism revealed age-dependent decrease in basal oxygen consumption rate, a general decrease in mitochondrial oxidative phosphorylation parameters, and loss in mitochondrial sparing capacity in both genotypes. Finally, we observed age-dependent increase in 3-nitrotyrosine residues in the hippocampus, consistent with a putative shift in (•)NO bioactivity toward oxidative chemistry associated with neurotoxicity.

Copyright © 2016 Elsevier Inc. All rights reserved. Keywords: Alzheimer's disease, Glutamate, High-resolution respirometry, Hippocampus, Microelectrode, Nitric oxide

O2k-Network Lab: PT Coimbra Laranjinha J


Labels: MiParea: Respiration  Pathology: Aging;senescence, Alzheimer's 

Organism: Mouse  Tissue;cell: Nervous system  Preparation: Permeabilized tissue 


Coupling state: LEAK, ET  Pathway: N, S, ROX  HRR: Oxygraph-2k