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. 2019 May 28:12:132.
doi: 10.3389/fnmol.2019.00132. eCollection 2019.

Neuronal Cells Rearrangement During Aging and Neurodegenerative Disease: Metabolism, Oxidative Stress and Organelles Dynamic

Affiliations

Neuronal Cells Rearrangement During Aging and Neurodegenerative Disease: Metabolism, Oxidative Stress and Organelles Dynamic

Vanessa Castelli et al. Front Mol Neurosci. .

Abstract

Brain cells normally respond adaptively to oxidative stress or bioenergetic challenges, resulting from ongoing activity in neuronal circuits. During aging and in neurodegenerative disorders, these mechanisms are compromised. In fact, neurons show unique age-related changes in functions and metabolism, resulting in greater susceptibility to insults and disease. Aging affects the nervous system as well as other organs. More precisely, as the nervous system ages, neuron metabolism may change, inducing glucose hypometabolism, impaired transport of critical substrates underlying metabolism, alterations in calcium signaling, and mitochondrial dysfunction. Moreover, in neuronal aging, an accumulation of impaired and aggregated proteins in the cytoplasm and in mitochondria is observed, as the result of oxidative stress: reduced antioxidant defenses and/or increase of reactive oxygen species (ROS). These changes lead to greater vulnerability of neurons in various regions of the brain and increased susceptibility to several diseases. Specifically, the first part of the review article will focus on the major neuronal cells' rearrangements during aging in response to changes in metabolism and oxidative stress, while the second part will cover the neurodegenerative disease areas in detail.

Keywords: aging; energetic metabolism; mitochondrial dysfunction; neurodegeneration; oxidative stress.

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Figures

Figure 1
Figure 1
Effect of aging in neuronal cell and involved mechanisms.
Figure 2
Figure 2
Effect of degeneration in neuronal cell and involved mechanisms.

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References

    1. Aarsland D., Creese B., Politis M., Chaudhuri K. R., Ffytche D. H., Weintraub D., et al. . (2017). Cognitive decline in Parkinson disease. Nat. Rev. Neurol. 13, 217–231. 10.1038/nrneurol.2017.27 - DOI - PMC - PubMed
    1. Abd El Mohsen M. M., Iravani M. M., Spencer J. P. E., Rose S., Fahim A. T., Motawi T. M. K., et al. . (2005). Age-associated changes in protein oxidation and proteasome activities in rat brain: modulation by antioxidants. Biochem. Biophys. Res. Commun. 336, 386–391. 10.1016/j.bbrc.2005.07.201 - DOI - PubMed
    1. Abramov A. Y., Duchen M. R. (2005). The role of an astrocytic NADPH oxidase in the neurotoxicity of amyloid β peptides. Philos. Trans. R. Soc. Lond. B Biol. Sci. 360, 2309–2314. 10.1098/rstb.2005.1766 - DOI - PMC - PubMed
    1. Aksam E. B., Koek A., Kiel J. A. K. W., Jourdan S., Veenhuis M., van der Klei I. J. (2007). A peroxisomal lon protease and peroxisome degradation by autophagy play key roles in vitality of Hansenula polymorpha cells. Autophagy 3, 96–105. 10.4161/auto.3534 - DOI - PubMed
    1. Albrecht P., Lewerenz J., Dittmer S., Noack R., Maher P., Methner A. (2010). Mechanisms of oxidative glutamate toxicity: the glutamate/cystine antiporter system xc as a neuroprotective drug target. CNS Neurol. Disord. Drug Targets 9, 373–382. 10.2174/187152710791292567 - DOI - PubMed

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