Abstract

Ferroptosis is a newly discovered form of necrotic cell death characterized by its dependency on iron and lipid peroxidation. Ferroptosis has attracted much attention recently in the area of neurodegeneration since the involvement of ferroptosis in Parkinson’s disease (PD), a major neurodegenerative disease, has been indicated using animal models. Although PD is associated with both genetic and environmental factors, sporadic forms of PD account for more than 90% of total PD. Following the importance of environmental factors, various neurotoxins are used as chemical inducers of PD both in vivo and in vitro. In contrast to other neurodegenerative diseases such as Alzheimer’s and Huntington’s diseases (AD and HD), many of the characteristics of PD can be reproduced in vivo by the use of specific neurotoxins. Given the indication of ferroptosis in PD pathology, several studies have been conducted to examine whether ferroptosis plays role in the loss of dopaminergic neurons in PD. However, there are still few reports showing an authentic form of ferroptosis in neuronal cells during exposure to the neurotoxins used as PD inducers. In this review article, we summarize the history of the uses of chemicals to create PD models in vivo and in vitro. Besides, we also survey recent reports examining the possible involvement of ferroptosis in chemical models of PD.

Highlights

  • Parkinson’s disease (PD) is a chronic, progressive, and irreversible neurodegenerative disorder, first medically described by James Parkinson in 1817 (Parkinson, 2002)

  • PD is characterized by a decrease in dopamine levels in the substantia nigra and subsequent loss of dopaminergic neurons

  • Given the importance of synuclein as well as dopamine, Lund human mesencephalic (LUHMES) cells might be a better choice than SH-SY5Y cells for the study of ferroptosis in PD models

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Summary

Frontiers in Cellular Neuroscience

Ferroptosis has attracted much attention recently in the area of neurodegeneration since the involvement of ferroptosis in Parkinson’s disease (PD), a major neurodegenerative disease, has been indicated using animal models. Following the importance of environmental factors, various neurotoxins are used as chemical inducers of PD both in vivo and in vitro. In contrast to other neurodegenerative diseases such as Alzheimer’s and Huntington’s diseases (AD and HD), many of the characteristics of PD can be reproduced in vivo by the use of specific neurotoxins. There are still few reports showing an authentic form of ferroptosis in neuronal cells during exposure to the neurotoxins used as PD inducers. We summarize the history of the uses of chemicals to create PD models in vivo and in vitro. We survey recent reports examining the possible involvement of ferroptosis in chemical models of PD

INTRODUCTION
BRAIN PATHOPHYSIOLOGY OF PD
CELLULAR PATHOPHYSIOLOGY OF PD
CHEMICALS USED TO CREATE PD MODEL
Findings
AUTHOR CONTRIBUTIONS
Full Text
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