1. Mitochondrial Dysfunction in Huntington Disease
- Author
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Md. Hafiz Uddin, Tasnuva Sarowar, and Marufa Rumman
- Subjects
medicine.anatomical_structure ,Mitochondrial Turnover ,medicine ,Mitochondrial fission ,Disease ,Neuron ,Biology ,Mitochondrion ,Function (biology) ,Biogenesis ,Intracellular organelles ,Cell biology - Abstract
This chapter discusses the processes essential for the maintenance of healthy mitochondria, as well as the contribution of mitochondrial dysfunction in the pathophysiology of Huntington’s disease. Mitochondria are well-adapted endosymbiotic intracellular organelles, which have acquired efficiency for energy production during the course of evolution. The brain is exceptionally dependent on mitochondria due to its high oxygen demand and sensitivity to oxidative damage. In a healthy neuron, mitochondria maintain a balance through mitochondrial fission, fusion, biogenesis, metabolism. Mitochondria grow like a tubular network, and if any part becomes damaged due to certain physiological processes, it separates the damaged part by the process of fission. Mitochondrial dysfunction is a common feature in neurodegenerative disorders as well as aging and other diseases. The lack of balance between mitochondrial fission and fusion negatively affects mitochondrial turnover. Modification of mitochondrial dynamics through fission and fusion accounts for the dysregulation of mitochondrial morphology, length, size, number, function, and distribution, and plays a deleterious role in neuronal health.
- Published
- 2020
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