Oxidative Stress and Neurodegeneration: Interconnected Processes in PolyQ Diseases.
Ioannis GkekasAnna GioranMarina Kleopatra BozikiNikolaos GrigoriadisNiki ChondrogianniSpyros PetrakisPublished in: Antioxidants (Basel, Switzerland) (2021)
Neurodegenerative polyglutamine (polyQ) disorders are caused by trinucleotide repeat expansions within the coding region of disease-causing genes. PolyQ-expanded proteins undergo conformational changes leading to the formation of protein inclusions which are associated with selective neuronal degeneration. Several lines of evidence indicate that these mutant proteins are associated with oxidative stress, proteasome impairment and microglia activation. These events may correlate with the induction of inflammation in the nervous system and disease progression. Here, we review the effect of polyQ-induced oxidative stress in cellular and animal models of polyQ diseases. Furthermore, we discuss the interplay between oxidative stress, neurodegeneration and neuroinflammation using as an example the well-known neuroinflammatory disease, Multiple Sclerosis. Finally, we review some of the pharmaceutical interventions which may delay the onset and progression of polyQ disorders by targeting disease-associated mechanisms.
Keyphrases
- oxidative stress
- multiple sclerosis
- dna damage
- ischemia reperfusion injury
- diabetic rats
- induced apoptosis
- healthcare
- gene expression
- physical activity
- molecular dynamics simulations
- genome wide
- spinal cord
- spinal cord injury
- single molecule
- cerebral ischemia
- blood brain barrier
- binding protein
- endoplasmic reticulum stress
- heat stress
- protein protein