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

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Specialty Molecular Biology
Date 2019 Jun 14
PMID 31191244
Citations 106
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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.

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References
1.
Reddy P, Williams M, Tagle D . Recent advances in understanding the pathogenesis of Huntington's disease. Trends Neurosci. 1999; 22(6):248-55. DOI: 10.1016/s0166-2236(99)01415-0. View

2.
Perkins A, Hendrie H, Callahan C, Gao S, Unverzagt F, Xu Y . Association of antioxidants with memory in a multiethnic elderly sample using the Third National Health and Nutrition Examination Survey. Am J Epidemiol. 1999; 150(1):37-44. DOI: 10.1093/oxfordjournals.aje.a009915. View

3.
Schultz S, OLeary D, Boles Ponto L, WATKINS G, Hichwa R, Andreasen N . Age-related changes in regional cerebral blood flow among young to mid-life adults. Neuroreport. 1999; 10(12):2493-6. DOI: 10.1097/00001756-199908200-00011. View

4.
Barja G, Herrero A . Oxidative damage to mitochondrial DNA is inversely related to maximum life span in the heart and brain of mammals. FASEB J. 2000; 14(2):312-8. DOI: 10.1096/fasebj.14.2.312. View

5.
Kohen R, Vellaichamy E, Hrbac J, Gati I, Tirosh O . Quantification of the overall reactive oxygen species scavenging capacity of biological fluids and tissues. Free Radic Biol Med. 2000; 28(6):871-9. DOI: 10.1016/s0891-5849(00)00191-x. View