» Articles » PMID: 38927274

Harnessing Mitochondrial Stress for Health and Disease: Opportunities and Challenges

Overview
Journal Biology (Basel)
Publisher MDPI
Specialty Biology
Date 2024 Jun 27
PMID 38927274
Authors
Affiliations
Soon will be listed here.
Abstract

Mitochondria, essential organelles orchestrating cellular metabolism, have emerged as central players in various disease pathologies. Recent research has shed light on mitohormesis, a concept proposing an adaptive response of mitochondria to minor disturbances in homeostasis, offering novel therapeutic avenues for mitochondria-related diseases. This comprehensive review explores the concept of mitohormesis, elucidating its induction mechanisms and occurrence. Intracellular molecules like reactive oxygen species (ROS), calcium, mitochondrial unfolded proteins (UPRmt), and integrated stress response (ISR), along with external factors such as hydrogen sulfide (HS), physical stimuli, and exercise, play pivotal roles in regulating mitohormesis. Based on the available evidence, we elucidate how mitohormesis maintains mitochondrial homeostasis through mechanisms like mitochondrial quality control and mitophagy. Furthermore, the regulatory role of mitohormesis in mitochondria-related diseases is discussed. By envisioning future applications, this review underscores the significance of mitohormesis as a potential therapeutic target, paving the way for innovative interventions in disease management.

Citing Articles

Synergistic Cellular Responses Conferred by Concurrent Optical and Magnetic Stimulation Are Attenuated by Simultaneous Exposure to Streptomycin: An Antibiotic Dilemma.

Iversen J, Frohlich J, Tai Y, Franco-Obregon A Bioengineering (Basel). 2024; 11(7).

PMID: 39061719 PMC: 11274164. DOI: 10.3390/bioengineering11070637.

References
1.
Powers S, Jackson M . Exercise-induced oxidative stress: cellular mechanisms and impact on muscle force production. Physiol Rev. 2008; 88(4):1243-76. PMC: 2909187. DOI: 10.1152/physrev.00031.2007. View

2.
Tu B, Kudlicki A, Rowicka M, McKnight S . Logic of the yeast metabolic cycle: temporal compartmentalization of cellular processes. Science. 2005; 310(5751):1152-8. DOI: 10.1126/science.1120499. View

3.
Park D, Kim J, Kim C . The effect of SIRT1 protein knock down on PGC-1α acetylation during skeletal muscle contraction. J Exerc Nutrition Biochem. 2015; 18(1):1-7. PMC: 4241934. DOI: 10.5717/jenb.2014.18.1.1. View

4.
Devi L, Raghavendran V, Prabhu B, Avadhani N, Anandatheerthavarada H . Mitochondrial import and accumulation of alpha-synuclein impair complex I in human dopaminergic neuronal cultures and Parkinson disease brain. J Biol Chem. 2008; 283(14):9089-100. PMC: 2431021. DOI: 10.1074/jbc.M710012200. View

5.
Nicholson C, Lambert J, Molkentin J, Sadoshima J, Calvert J . Thioredoxin 1 is essential for sodium sulfide-mediated cardioprotection in the setting of heart failure. Arterioscler Thromb Vasc Biol. 2013; 33(4):744-51. PMC: 3827725. DOI: 10.1161/ATVBAHA.112.300484. View