Hypoxia Sensing and Responses in Parkinson’s Disease

Author:

Burtscher Johannes1ORCID,Duderstadt Yves234,Gatterer Hannes5ORCID,Burtscher Martin6ORCID,Vozdek Roman7ORCID,Millet Grégoire P.1ORCID,Hicks Andrew A.7ORCID,Ehrenreich Hannelore89ORCID,Kopp Martin6ORCID

Affiliation:

1. Institute of Sport Sciences, University of Lausanne, 1015 Lausanne, Switzerland

2. Division of Cardiology and Angiology, University Hospital Magdeburg, 39120 Magdeburg, Germany

3. Research Group Neuroprotection, German Center for Neurodegenerative Diseases (DZNE), 39120 Magdeburg, Germany

4. Department of Sports Science, Otto-von-Guericke University, 39120 Magdeburg, Germany

5. Institute of Mountain Emergency Medicine, Eurac Research, 39100 Bolzano, Italy

6. Department of Sport Science, University of Innsbruck, 6020 Innsbruck, Austria

7. Institute for Biomedicine, Eurac Research, Via Alessandro Volta 21, 39100 Bolzano, Italy

8. Clinical Neuroscience, Max Planck Institute for Multidisciplinary Sciences, 37075 Goettingen, Germany

9. Experimental Medicine, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, 68159 Mannheim, Germany

Abstract

Parkinson’s disease (PD) is associated with various deficits in sensing and responding to reductions in oxygen availability (hypoxia). Here we summarize the evidence pointing to a central role of hypoxia in PD, discuss the relation of hypoxia and oxygen dependence with pathological hallmarks of PD, including mitochondrial dysfunction, dopaminergic vulnerability, and alpha-synuclein-related pathology, and highlight the link with cellular and systemic oxygen sensing. We describe cases suggesting that hypoxia may trigger Parkinsonian symptoms but also emphasize that the endogenous systems that protect from hypoxia can be harnessed to protect from PD. Finally, we provide examples of preclinical and clinical research substantiating this potential.

Publisher

MDPI AG

Reference107 articles.

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