Title | Strategies to protect against age-related mitochondrial decay: Do natural products and their derivatives help? |
Publication Type | Journal Article |
Year of Publication | 2022 |
Authors | Visioli F, Ingram A, Beckman JS, Magnusson KR, Hagen TM |
Journal | Free Radic Biol Med |
Volume | 178 |
Pagination | 330-346 |
Date Published | 2022 Jan |
ISSN | 1873-4596 |
Keywords | Animals, Antioxidants, Biological Products, Humans, Mitochondria, Mitophagy, Oxidative Stress |
Abstract | Mitochondria serve vital roles critical for overall cellular function outside of energy transduction. Thus, mitochondrial decay is postulated to be a key factor in aging and in age-related diseases. Mitochondria may be targets of their own decay through oxidative damage. However, treating animals with antioxidants has been met with only limited success in rejuvenating mitochondrial function or in increasing lifespan. A host of nutritional strategies outside of using traditional antioxidants have been devised to promote mitochondrial function. Dietary compounds are under study that induce gene expression, enhance mitochondrial biogenesis, mitophagy, or replenish key metabolites that decline with age. Moreover, redox-active compounds may now be targeted to mitochondria which improve their effectiveness. Herein we review the evidence that representative dietary effectors modulate mitochondrial function by stimulating their renewal or reversing the age-related loss of key metabolites. While in vitro evidence continues to accumulate that many of these compounds benefit mitochondrial function and/or prevent their decay, the results using animal models and, in some instances human clinical trials, are more mixed and sometimes even contraindicated. Thus, further research on optimal dosage and age of intervention are warranted before recommending potential mitochondrial rejuvenating compounds for human use. |
DOI | 10.1016/j.freeradbiomed.2021.12.008 |
Alternate Journal | Free Radic Biol Med |
PubMed ID | 34890770 |
Grant List | R21 AG060206 / AG / NIA NIH HHS / United States |