Mitochondrial metabolism in major neurological diseases

Zhengqiu Zhou, Grant L. Austin, Lyndsay E.A. Young, Lance A. Johnson, Ramon Sun

Research output: Contribution to journalReview articlepeer-review

43 Scopus citations

Abstract

Mitochondria are bilayer sub-cellular organelles that are an integral part of normal cellular physiology. They are responsible for producing the majority of a cell’s ATP, thus supplying energy for a variety of key cellular processes, especially in the brain. Although energy production is a key aspect of mitochondrial metabolism, its role extends far beyond energy production to cell signaling and epigenetic regulation–functions that contribute to cellular proliferation, differentiation, apoptosis, migration, and autophagy. Recent research on neurological disorders suggest a major metabolic component in disease pathophysiology, and mitochondria have been shown to be in the center of metabolic dysregulation and possibly disease manifestation. This review will discuss the basic functions of mitochondria and how alterations in mitochondrial activity lead to neurological disease progression.

Original languageEnglish
Article number229
JournalCells
Volume7
Issue number12
DOIs
StatePublished - Dec 2018

Bibliographical note

Publisher Copyright:
© 2018 by the authors. Licensee MDPI, Basel, Switzerland.

Keywords

  • Alzheimer’s disease
  • Epilepsy
  • Metabolism
  • Mitochondria
  • Traumatic brain injury

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology

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