Bioenergetics, aging and neurodegenerative diseases
Author:
Srebro, Zbigniew
Lach, Henryk
Publisher:
Wydawnictwo Naukowe Wyższej Szkoły Pedagogicznej, Kraków
xmlui.dri2xhtml.METS-1.0.item-isbn: 83-85898-66-2
xmlui.dri2xhtml.METS-1.0.item-issn: 0239-6025
xmlui.dri2xhtml.METS-1.0.item-iso: en
Date: 1996
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3rd edition, extended and revised. This monograph was printed thanks to partial financial support by the Committee for Scientific Research of the Republic of Poland.Abstract
The first part of the book describes normal neuronal
metabolism, particularly in respect to energy metabolism. The
main energy metabolism of neurons is in the mitochondrial
generation of ATP, the latter being obtained also from
glycolysis, but to a much lesser extent. The role of
neurotransmitters, trophic factors, calcium and growth factors
is discussed.
The second part contains data on the normal aging of
neurons and the decline of energy metabolism in aging
cells. Data are discussed which indicate that aging cells are
subject to increasing oxidative stress due to insufficient
antioxidant defences. During aging, increasing amounts of
active oxygen species and oxygen radicals are produced
within the cell, which damage cellular macromolecules with
the resulting structural and biochemical deterioration. A kind
of pathologic positive feedback does occur, which further
damages the cell's organizational structure and the energy
producing enzymatic machinery. The ultimate outcome of
these processes is cell damage and death. A similar sequence
of events is taking place in the course of Alzheimer's disease
and other neurodegenerative syndromes.
The pathomechanism of Alzheimer's disease and other
neurodegenerative diseases is described and discussed in the
third part of the book. It is proposed that a final common
pathway in the development of both aging and neurodegenerative
diseases is the hypometabolism with energetic
insufficiency and a devastating oxidative stress. The neuropathology
of Alzheimer's disease can be explained in most
cases by a decline in cellular ATP available for normal
functioning of the neurons. Decreased ATP levels are
the cause of aberrant protein conformation, and aberrant
intraneuronal transport of structural proteins and organelles.
The oxidative stress accompanying the hypometabolism
causes irreversible damage to the neuron's DNA and proteins
and leads to cytomembrane lipids' peroxidation. A positive
feedback between the decreased metabolism and oxygen stress
on the one hand, and structural changes in the cell on the other,
leads to irreversible damage to the neurons with consequent
neuropathology and cell death.
The discussed pathomechanism of aging and neurodegenerative
diseases may allow a new approach to the treatment
of these diseases. Such new approaches are suggested and
discussed.