Abstract

In aging and neurodegenerative diseases, loss of distinct type of neurons characterizes disease-specific pathological and clinical features, and mitochondria play a pivotal role in neuronal survival and death. Mitochondria are now considered as the organelle to modulate cellular signal pathways and functions, not only to produce energy and reactive oxygen species. Oxidative stress, deficit of neurotrophic factors, and multiple other factors impair mitochondrial function and induce cell death. Multi-functional plant polyphenols, major groups of phytochemicals, are proposed as one of most promising mitochondria-targeting medicine to preserve the activity and structure of mitochondria and neurons. Polyphenols can scavenge reactive oxygen and nitrogen species and activate redox-responsible transcription factors to regulate expression of genes, coding antioxidants, anti-apoptotic Bcl-2 protein family, and pro-survival neurotrophic factors. In mitochondria, polyphenols can directly regulate the mitochondrial apoptosis system either in preventing or promoting way. Polyphenols also modulate mitochondrial biogenesis, dynamics (fission and fusion), and autophagic degradation to keep the quality and number. This review presents the role of polyphenols in regulation of mitochondrial redox state, death signal system, and homeostasis. The dualistic redox properties of polyphenols are associated with controversial regulation of mitochondrial apoptosis system involved in the neuroprotective and anti-carcinogenic functions. Mitochondria-targeted phytochemical derivatives were synthesized based on the phenolic structure to develop a novel series of neuroprotective and anticancer compounds, which promote the bioavailability and effectiveness. Phytochemicals have shown the multiple beneficial effects in mitochondria, but further investigation is required for the clinical application.

Highlights

  • More than 1.5 billion years ago, mitochondria originate from bacterial endosymbions within some ancestral type of eukaryotic cells containing the nucleus, cytoskeleton, and endomembrane system, but lacking mitochondria [1]

  • Mitochondria are implicated in regulation of cellular redox potency, which is important for normal physiological processes [2], the deregulation of which is associated with the pathogenesis of aging, neurodegenerative diseases, such as Parkinson’s and Alzheimer’s disease (PD, AD), cardiovascular diseases, inflammation, and metabolic disorders

  • Apoptosis is initiated with mitochondrial membrane permeability transition (MPT), a sudden increase in membrane permeability, followed by opening of the non-specific mega-channel called the mitochondrial permeability transition pore, and release of apoptosis-executing molecules, such as cytochrome c (Cytc), second mitochondria-derived activator of caspases (Smac)/Diablo, apoptosis-inducing factor (AIF), and endonuclease G, from the matrix to the cytoplasm

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Summary

Introduction

More than 1.5 billion years ago, mitochondria originate from bacterial endosymbions within some ancestral type of eukaryotic cells containing the nucleus, cytoskeleton, and endomembrane system, but lacking mitochondria [1]. The function of the TSPO and TspO is conserved through revolution, suggesting that TSPO may be developed from TspO the ancient bacterial receptor/stress sensor to play roles in the outer mitochondrial membrane (OMM) of eukaryotes [5,6] These results suggest that mitochondria have their own death system to decide the fate of host cells and function as a foe within. Novel antioxidant-independent neuroprotective functions have been confirmed: direct regulation of the MPT, modulation of cellular signal pathways, and induction of genes coding anti-apoptotic Bcl-2 protein family and NTFs, especially brain-derived and glial cell line-derived neurotrophic factor (BDNF, GDNF) [16,17,18]. Oxidative Stress and Mitochondrial Dysfunction are the Major Pathogenic Factors in Neurodegeneration

Production of Reactive Oxidative Species and Mitochondrial Dysfunction
Structure and Regulation of Mitochondrial Apoptosis System
H H H Gallate
Polyphenols Influence Mitochondrial Fission and Fusion
Polyphenols Affect Mitophagy and Control Mitochondrial Quality
Synthesis of Mitochondria-Targeting Polyphenols
Discussion
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