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Mitochondrial dysfunctions in neurodegenerative diseases: role in disease pathogenesis, strategies for analysis and therapeutic prospects.
Rey, Federica; Ottolenghi, Sara; Zuccotti, Gian Vincenzo; Samaja, Michele; Carelli, Stephana.
Afiliación
  • Rey F; Department of Biomedical and Clinical Sciences "L. Sacco", University of Milan; Paediatric Clinical Research Centre Fondazione "Romeo ed Enrica Invernizzi", University of Milano, Milano, Italy.
  • Ottolenghi S; Laboratory of Biochemistry, Department of Health Sciences, University of Milan, Milano, Italy.
  • Zuccotti GV; Department of Biomedical and Clinical Sciences "L. Sacco", University of Milan; Paediatric Clinical Research Centre Fondazione "Romeo ed Enrica Invernizzi", University of Milano; Department of Paediatrics, Children's Hospital "V. Buzzi", Milano, Italy.
  • Samaja M; Laboratory of Biochemistry, Department of Health Sciences, University of Milan, Milano, Italy.
  • Carelli S; Department of Biomedical and Clinical Sciences "L. Sacco", University of Milan; Paediatric Clinical Research Centre Fondazione "Romeo ed Enrica Invernizzi", University of Milano, Milano, Italy.
Neural Regen Res ; 17(4): 754-758, 2022 Apr.
Article en En | MEDLINE | ID: mdl-34472461
Fundamental organelles that occur in every cell type with the exception of mammal erythrocytes, the mitochondria are required for multiple pivotal processes that include the production of biological energy, the biosynthesis of reactive oxygen species, the control of calcium homeostasis, and the triggering of cell death. The disruption of anyone of these processes has been shown to impact strongly the function of all cells, but especially of neurons. In this review, we discuss the role of the mitochondria impairment in the development of the neurodegenerative diseases Amyotrophic Lateral Sclerosis, Parkinson's disease and Alzheimer's disease. We highlight how mitochondria disruption revolves around the processes that underlie the mitochondria's life cycle: fusion, fission, production of reactive oxygen species and energy failure. Both genetic and sporadic forms of neurodegenerative diseases are unavoidably accompanied with and often caused by the dysfunction in one or more of the key mitochondrial processes. Therefore, in order to get in depth insights into their health status in neurodegenerative diseases, we need to focus into innovative strategies aimed at characterizing the various mitochondrial processes. Current techniques include Mitostress, Mitotracker, transmission electron microscopy, oxidative stress assays along with expression measurement of the proteins that maintain the mitochondrial health. We will also discuss a panel of approaches aimed at mitigating the mitochondrial dysfunction. These include canonical drugs, natural compounds, supplements, lifestyle interventions and innovative approaches as mitochondria transplantation and gene therapy. In conclusion, because mitochondria are fundamental organelles necessary for virtually all the cell functions and are severely impaired in neurodegenerative diseases, it is critical to develop novel methods to measure the mitochondrial state, and novel therapeutic strategies aimed at improving their health.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies Aspecto: Patient_preference Idioma: En Revista: Neural Regen Res Año: 2022 Tipo del documento: Article País de afiliación: Italia Pais de publicación: India

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies Aspecto: Patient_preference Idioma: En Revista: Neural Regen Res Año: 2022 Tipo del documento: Article País de afiliación: Italia Pais de publicación: India