Dysfunction of mitochondria as the basis of Parkinson's disease

1Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Parkinson's disease is the second most common neurodegenerative disease, affecting about 0,15-0,3% of the world's population. Its characteristic feature is a loss of dopaminergic neurons in the substantia nigra. PD leads to dopamine deficiency and formation of intracellular inclusions called Lewy bodies, whose main ingredient is α-synuclein. Other types of nervous system cells are also affected by changes associated with that disease. The underlying molecular pathogenesis involves multiple pathways and mechanisms: Mitochondrial function, oxidative stress, genetic factors, α-synuclein proteostasis, mitochondrial dynamic impairment, and disorders of the mitophagy process. This review summarizes the factors affecting the functioning of the mitochondria and their connection to the development of Parkinson's disease.

Cite

CITATION STYLE

APA

Popis, M. (2018). Dysfunction of mitochondria as the basis of Parkinson’s disease. Medical Journal of Cell Biology, 6(4), 174–181. https://doi.org/10.2478/acb-2018-0027

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free