Mitochondrial medicine for neurodegenerative diseases |
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Authors: | Heng Du Shirley ShiDu Yan |
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Affiliation: | 1. Neuroscience Graduate Program, University of Alabama at Birmingham, 35294, USA;2. Department of Neurology, University of Alabama at Birmingham, 35294, USA;3. Department of Neurobiology, University of Alabama at Birmingham, 35294, USA;4. Department of Psychiatry & Behavioral Neurobiology, University of Alabama at Birmingham, 35294, USA;1. Department of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, Laboratory for Technologies of Advanced Therapies (LTTA), University of Ferrara, Ferrara, Italy;2. Cardiovascular Institute, Azienda Ospedaliero-Universitaria S. Anna and LTTA Center, Ferrara, Italy;3. Department of Biochemistry, Nencki Institute of Experimental Biology, Warsaw, Poland |
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Abstract: | Mitochondrial dysfunction has been reported in a wide array of neurological disorders ranging from neuromuscular to neurodegenerative diseases. Recent studies on neurodegenerative diseases have revealed that mitochondrial pathology is generally found in inherited or sporadic neurodegenerative diseases and is believed to be involved in the pathophysiological process of these diseases. Commonly seen types of mitochondrial dysfunction in neurodegenerative diseases include excessive free radical generation, lowered ATP production, mitochondrial permeability transition, mitochondrial DNA lesions, perturbed mitochondrial dynamics and apoptosis. Mitochondrial medicine as an emerging therapeutic strategy targeted to mitochondrial dysfunction in neurodegenerative diseases has been proven to be of value, though this area of research is still at in its early stage. In this article, we report on recent progress in the development of several mitochondrial therapies including antioxidants, blockade of mitochondrial permeability transition, and mitochondrial gene therapy as evidence that mitochondrial medicine has promise in the treatment of neurodegenerative diseases. |
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