Metal dyshomeostasis and their pathological role in prion and prion-like diseases: The basis for a nutritional approach
Academic Article
Publication Date:
2017
abstract:
Metal ions are key elements in organisms' life acting like cofactors of many enzymes
but they can also be potentially dangerous for the cell participating in redox reactions
that lead to the formation of reactive oxygen species (ROS). Any factor inducing or
limiting a metal dyshomeostasis, ROS production and cell injury may contribute to the
onset of neurodegenerative diseases or play a neuroprotective action. Transmissible
spongiform encephalopathies (TSEs), also known as prion diseases, are a group of fatal
neurodegenerative disorders affecting the central nervous system (CNS) of human and
other mammalian species. The causative agent of TSEs is believed to be the scrapie
prion protein PrPSc, the ? sheet-rich pathogenic isoform produced by the conformational
conversion of the ?-helix-rich physiological isoform PrPC. The peculiarity of PrPSc is its
ability to self-propagate in exponential fashion in cells and its tendency to precipitate
in insoluble and protease-resistance amyloid aggregates leading to neuronal cell death.
The expression "prion-like diseases" refers to a group of neurodegenerative diseases that
share some neuropathological features with prion diseases such as the involvement of
proteins (?-synuclein, amyloid ?, and tau) able to precipitate producing amyloid deposits
following conformational change. High social impact diseases such as Alzheimer's and
Parkinson's belong to prion-like diseases. Accumulating evidence suggests that the
exposure to environmental metals is a risk factor for the development of prion and
prion-like diseases and that metal ions can directly bind to prion and prion-like proteins
affecting the amount of amyloid aggregates. The diet, source of metal ions but also of
natural antioxidant and chelating agents such as polyphenols, is an aspect to take into
account in addressing the issue of neurodegeneration. Epidemiological data suggest
that the Mediterranean diet, based on the abundant consumption of fresh vegetables
and on low intake of meat, could play a preventive or delaying role in prion and prion-like
neurodegenerative diseases. In this review, metal role in the onset of prion and p
Iris type:
01.01 Articolo in rivista
Keywords:
Alzheimer's disease; Mediterranean diet; Metal dyshomeostasis; Parkinson's disease; Prion; Synuclein; Synucleinopathies; Transmissible spongiform encephalopathies
List of contributors:
Massimino, MARIA LINA
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