Literature DB >> 30072093

Mitohormesis, an Antiaging Paradigm.

Clea Bárcena1, Pablo Mayoral1, Pedro M Quirós2.   

Abstract

Mitohormesis is a term used to define a biological response where the induction of a reduced amount of mitochondrial stress leads to an increment in health and viability within a cell, tissue, or organism. The mitochondrial stress response activated by a potentially damaging stimulus requires a coordinated dialogue with the cellular nucleus, known as mitonuclear communication. This interplay induced by the hormetic response in mitochondria relies in a variety of signals among which the most relevant ones are reactive oxygen species (ROS), mitochondrial metabolites, proteotoxic signals, the mitochondria-cytosol stress response, and the release of mitokines. The activation of the mitohormetic response increases lifespan in different animal models, from worms to mammals. Further, mitohormesis also enhances healthspan, particularly improving metabolism and immune system. Although multiple mediators and stress signals have been proposed to activate this protective mechanism, beneficial outcomes of mitohormesis are most probably due to an increase in mitochondrial ROS. Activation of other protective stress mechanisms as mitochondrial unfolded protein response or the increase in the expression of mitokines are also associated with the positive benefits exerted by mitohormesis. Herein, we review the different mitohormetic signals and pathways described from worms to mammals and their effects on health and survival. The identification and description of pathways and molecules implicated in the beneficial effects of mitohormesis will help understand the complex balance between death and survival in the face of mitochondrial damage and will allow to open a novel area of therapies aimed at improving health in humans.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Aging; Hormesis; Mitochondria; Mitokine; ROS; UPR(mt)

Mesh:

Substances:

Year:  2018        PMID: 30072093     DOI: 10.1016/bs.ircmb.2018.05.002

Source DB:  PubMed          Journal:  Int Rev Cell Mol Biol        ISSN: 1937-6448            Impact factor:   6.813


  37 in total

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Review 2.  Mitohormesis, UPRmt, and the Complexity of Mitochondrial DNA Landscapes in Cancer.

Authors:  Timothy C Kenny; Maria L Gomez; Doris Germain
Journal:  Cancer Res       Date:  2019-09-04       Impact factor: 12.701

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Review 4.  Redox Homeostasis Involvement in the Pharmacological Effects of Metformin in Systemic Lupus Erythematosus.

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Review 6.  Kynurenine pathway, NAD+ synthesis, and mitochondrial function: Targeting tryptophan metabolism to promote longevity and healthspan.

Authors:  Raul Castro-Portuguez; George L Sutphin
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7.  The AAA ATPase Afg1 preserves mitochondrial fidelity and cellular health by maintaining mitochondrial matrix proteostasis.

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Journal:  J Cell Sci       Date:  2018-11-21       Impact factor: 5.285

Review 8.  Rescuing mitochondria in traumatic brain injury and intracerebral hemorrhages - A potential therapeutic approach.

Authors:  Meenakshi Ahluwalia; Manish Kumar; Pankaj Ahluwalia; Scott Rahimi; John R Vender; Raghavan P Raju; David C Hess; Babak Baban; Fernando L Vale; Krishnan M Dhandapani; Kumar Vaibhav
Journal:  Neurochem Int       Date:  2021-09-22       Impact factor: 3.921

9.  Downregulation of DUOX1 function contributes to aging-related impairment of innate airway injury responses and accelerated senile emphysema.

Authors:  Caspar Schiffers; Lennart K A Lundblad; Milena Hristova; Aida Habibovic; Christopher M Dustin; Nirav Daphtary; Minara Aliyeva; David J Seward; Yvonne M W Janssen-Heininger; Emiel F M Wouters; Niki L Reynaert; Albert van der Vliet
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2021-05-05       Impact factor: 6.011

Review 10.  The Power of Stress: The Telo-Hormesis Hypothesis.

Authors:  Maria Sol Jacome Burbano; Eric Gilson
Journal:  Cells       Date:  2021-05-11       Impact factor: 6.600

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