Energy Compensation Strategy: The Frontier of Neurodegenerative Disease Treatment
Neurodegenerative diseases are a major threat to global public health. Recent studies have revealed that mitochondrial DNA damage and the imbalance of protein homeostasis during aging constitute the core pathological basis of neurodegeneration. The resulting energy metabolism disorders are the common pathogenic hubs of multiple neurodegenerative diseases. In this review, we focus on representative neurodegenerative diseases, including Parkinson's disease, Alzheimer's disease, and Huntington's disease, and systematically discuss their pathology related to metabolic disorders. We introduce various energy compensation strategies: (1) rebuilding the energy supply by enhancing mitochondrial function; (2) implementing systemic metabolic remodeling; (3) supplementing alternative energy substrates; (4) utilizing direct energy delivery technology. This review also highlights the technical bottlenecks of existing energy compensation strategies, guiding future research on neurodegenerative diseases.
Authors
- Junyue Tang
- Mimi Wan (ORCID: https://orcid.org/0000-0002-8686-7961)
- Yue Sun (ORCID: https://orcid.org/0000-0003-2682-3542)
- Xinyu Zhao (ORCID: https://orcid.org/0000-0002-5128-4424)
- Jie Li (ORCID: https://orcid.org/0000-0002-4366-7724)
- XingYu Lin (ORCID: https://orcid.org/0009-0007-4446-3209)
- Ya Guan (ORCID: https://orcid.org/0000-0002-6889-4966)
- Chun Mao
Institutions
- Qingdao University (CN)
- Nanjing Normal University (CN)
- Shanghai Jiao Tong University (CN)
- XinHua Hospital (CN)
- Institute of Molecular Functional Materials (CN)
- Affiliated Hospital of Qingdao University (CN)
- Jimo District Qingdao Hospital of Traditional Chinese Medicine (CN)
- Research Institute for Genetic and Human Therapy (US)
Publication Details
- Journal
- ACS Chemical Neuroscience
- Published
- 2026-03-12
- DOI
- https://doi.org/10.1021/acschemneuro.5c00964
- Primary Topic
- Amyotrophic Lateral Sclerosis Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00