4.7 Review

Boosting mitochondrial health to counteract neurodegeneration

Journal

PROGRESS IN NEUROBIOLOGY
Volume 215, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pneurobio.2022.102289

Keywords

Neurodegeneration; Mitochondria; Hormesis; Ageing; Conditioning; Exercise

Categories

Funding

  1. Defitech Foundation
  2. Bertarelli Foundation
  3. SNSF Lead Agency [NiBS-iCog 320030L_197899]

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Mitochondrial health is crucial for the treatment of neurodegenerative diseases, but current therapeutic strategies targeting specific mitochondrial stressors have not shown clear clinical benefits. Promoting the capacity of mitochondria and other cellular components to restore a healthy cellular environment is a promising alternative approach. This study provides a non-technical overview of neuroprotective strategies targeting mitochondria, focusing on top-down interventions such as metabolic modulators, exercise, dietary restriction, brain stimulation, and conditioning.
Mitochondrial health is based on a delicate balance of specific mitochondrial functions (e.g. metabolism, signaling, dynamics) that are impaired in neurodegenerative diseases. Rescuing mitochondrial function by selectively targeting mitochondrial stressors, such as reactive oxygen species, inflammation or proteotoxic insults (bottom-up approaches) thus is a widely investigated therapeutic strategy. While successful in preclinical studies, these approaches have largely failed to show clear clinical benefits. Promoting the capacity of mitochondria - and other cellular components - to restore a healthy cellular environment is a promising complementary or alternative approach. Herein, we provide a non-technical overview for neurologists and scientists interested in brain metabolism on neuroprotective strategies targeting mitochondria and focus on top-down interventions such as metabolic modulators, exercise, dietary restriction, brain stimulation and conditioning. We highlight general conceptual differences to bottom-up approaches and provide hypotheses on how these mechanistically comparatively poorly characterized top-down therapies may work, discussing notably mitochondrial stress responses and mitohormesis.

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