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EDITORIAL article

Front. Pharmacol., 30 June 2023
Sec. Ethnopharmacology
This article is part of the Research Topic Natural Products in Regulating Mitochondrial Dysfunction View all 7 articles

Editorial: Natural products in regulating mitochondrial dysfunction

  • 1School of Basic Medical Sciences, Nanchang University, Nanchang, China
  • 2Division of Nephrology, Kidney Research Institute, West China Hospital of Sichuan University, Chengdu, China
  • 3Key Laboratory of Molecular Biology and Gene Engineering of Jiangxi Province, School of Life Sciences, Nanchang University, Nanchang, China
  • 4Graduate School of Agriculture, Hokkaido University, Sapporo, Japan

Mitochondria plays a central role in energy production for all multicellular eukaryotes by synthesizing ATP and maintaining metabolic homeostasis. Actually, these fantastic organelles perform multifunction for the cell beyond simply being a “fuel” (Nunnari and Suomalainen, 2012). Mitochondria not only governs many metabolic processes including oxidative phosphorylation (OXPHOS), electron transport chain (ETC), Krebs cycle, fatty acid oxidation, and many others, but also modulates cell proliferation, cell death, and even inflammatory response (Monzel et al., 2023). Damages caused by mitochondrial DNA (mtDNA) mutations or quality control disorders tend to accumulate in these organelles and led to mitochondrial dysfunction, which is characterized by a loss of efficiency in the electron transport chain and reductions in the synthesis of high-energy molecules. However, recent advances show that mitochondrial dysfunction is being recognized to be even more complex than originally thought (Vafai and Mootha, 2012; Sorrentino et al., 2018). Mitochondrial disease caused by mitochondrial dysfunction is associated with a wide range of human pathologies, such as cancer, metabolic, and cardiovascular diseases, autoimmune diseases, neurobehavioral and psychiatric diseases, neurodegenerative diseases, and so on (Lin and Beal, 2006; Prakash et al., 2017; Chiu et al., 2020).

There is currently no effective treatment for mitochondrial disease, especially for inherited mitochondrial diseases caused by either mtDNA or nuclear DNA mutations. The major management strategy for mitochondrial disease is supportive therapy including nutritional management, exercise, vitamin or amino acid supplements (El-Hattab et al., 2017; Zhong et al., 2022). It is hypothesized that natural products or compounds derived from traditional herbs with antioxidant or metabolic reprogramming capacity could be potential treatment options (Nicolson, 2014; Cho et al., 2019; Mohammadipour, 2022). Thus, it is necessary to explore more mitochondria protective agents, especially natural products, and fully understand the pathophysiology of the disease caused by mitochondrial dysfunction. The present Research Topic aims to provide a platform for communication of current scientific evidence available about the role of natural products in regulating mitochondrial dysfunction.

The present Research Topic features five articles, including one original and four review articles. These articles are dedicated to exploring the mechanism underlying the dysfunction of mitochondria and trying to find the way to ameliorate this disorder by natural products.

Non-alcoholic fatty liver disease (NAFLD) is the most common type of liver disease which finally would lead to liver failure and hepatocellular carcinoma. The mechanism underlying the development and progression of NAFLD is closely related to the dysfunction of mitochondria. Studies suggested that saturated fatty acids or impaired mitochondrial dynamics produce reactive oxygen species and endoplasmatic reticulum stress, which ultimately leads to inflammation, apoptosis, and liver scarring (Longo et al., 2021; Meex and Blaak, 2021). Therefore, targeting mitochondrial dysfunction is probably a potent therapeutic strategy for NAFLD. An original research article (García-Berumen et al.) regarding a novel treatment of NAFLD by restoring mitochondrial function was included in this Research Topic. Avocado oil extracted from the fruit of the avocado tree (Persea americana Mill.) was tested to evaluate its anti-NAFLD effect in vivo. The authors demonstrated that avocado oil alleviates NAFLD by attenuating mitochondrial dysfunction, oxidative stress, and inflammation. In this paper, avocado oil showed a protective effect on mitochondrial respiration, complex III activity, and electron transfer in cytochromes in complex III. The present study indicated that regulating mitochondrial function by natural products would be a potential way to ameliorate related diseases, especially metabolic disorders.

Four review papers (Chen et al.; Liu et al.; Tuo et al.; He et al.) were also included in this Research Topic. Chen et al. analyzed the database and summarized the recent advances in the field of mitochondrial dysfunction treated with natural products, and further discussed the role of natural products in modulating mitochondrial quality control systems and regulating mitochondrial functions. The authors concluded that increased research on mitochondria has facilitated the development of new strategies based on natural products to regulate mitochondrial dysfunction. While, at the same time, there are several challenges including dosage optimization, chemical structure modification, and target specificity lie ahead on the road of natural product development. Liu et al. and He et al. discussed the function of natural products in two typical mitochondrial dysfunction-related diseases (metabolic-associated kidney diseases and Parkinson’s disease), respectively. These two papers indicated that natural products were promising to be developed as drugs for the treatment of both metabolic and non-metabolic disorders by restoring mitochondrial dysfunction. However, the efficacy and dosage of natural products are not stable, and the structure-bioactivity relationship of natural products is complex and uncertain. These shortages would limit the application of natural products in the therapy of metabolic-associated kidney diseases and PD. Tuo et al. presented a scoping review on the role of natural products regulating mitochondrial function in cognitive dysfunction. Fourteen studies published from 15 October 2017 to 15 October 2022 were collected, integrated, analyzed, and summarized to assess the therapeutic effect of natural products on cognitive dysfunction. The authors indicated that natural products can improve or reduce cognitive dysfunction by ameliorating mitochondrial dysfunction. But, the limitation of this paper is that few studies were taken into analysis and the results are not so confirmed. Future work should be done to improve the quantity of samples and the quality of the analysis.

Overall, the studies collected in this Research Topic contribute to emphasizing the function of natural products in the regulation of mitochondrial dysfunction. We hope this series of publications will shed light on the intricate mechanisms involved and the development of novel therapeutic strategies for mitochondrial dysfunction.

Author contributions

All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.

Acknowledgments

The editors would like to express their gratitude to the authors for choosing this Research Topic to share their valuable studies and to Frontiers in Pharmacology for launching this Propolis Research Topic.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Chiu, H. Y., Tay, E. X. Y., Ong, D. S. T., and Taneja, R. (2020). Mitochondrial dysfunction at the center of cancer therapy. Antioxid. Redox Signal 32 (5), 309–330. doi:10.1089/ars.2019.7898

PubMed Abstract | CrossRef Full Text | Google Scholar

Cho, B., Kim, T., Huh, Y. J., Lee, J., and Lee, Y. I. (2019). Amelioration of mitochondrial quality control and proteostasis by natural compounds in Parkinson's disease models. Int. J. Mol. Sci. 20 (20), 5208. doi:10.3390/ijms20205208

PubMed Abstract | CrossRef Full Text | Google Scholar

El-Hattab, A. W., Zarante, A. M., Almannai, M., and Scaglia, F. (2017). Therapies for mitochondrial diseases and current clinical trials. Mol. Genet. Metab. 122 (3), 1–9. doi:10.1016/j.ymgme.2017.09.009

CrossRef Full Text | Google Scholar

Lin, M. T., and Beal, M. F. (2006). Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases. Nature 443 (7113), 787–795. doi:10.1038/nature05292

PubMed Abstract | CrossRef Full Text | Google Scholar

Longo, M., Meroni, M., Paolini, E., Macchi, C., and Dongiovanni, P. (2021). Mitochondrial dynamics and nonalcoholic fatty liver disease (NAFLD): New perspectives for a fairy-tale ending? Metabolism 117, 154708. doi:10.1016/j.metabol.2021.154708

PubMed Abstract | CrossRef Full Text | Google Scholar

Meex, R. C. R., and Blaak, E. E. (2021). Mitochondrial dysfunction is a key pathway that links saturated fat intake to the development and progression of NAFLD. Mol. Nutr. Food Res. 65 (1), e1900942. doi:10.1002/mnfr.201900942

PubMed Abstract | CrossRef Full Text | Google Scholar

Mohammadipour, A. (2022). A focus on natural products for preventing and cure of mitochondrial dysfunction in Parkinson's disease. Metab. Brain Dis. 37 (4), 889–900. doi:10.1007/s11011-022-00931-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Monzel, A. S., Enríquez, J. A., and Picard, M. (2023). Multifaceted mitochondria: Moving mitochondrial science beyond function and dysfunction. Nat. Metab. 5 (4), 546–562. doi:10.1038/s42255-023-00783-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Nicolson, G. L. (2014). Mitochondrial dysfunction and chronic disease: Treatment with natural supplements. Integr. Med. (Encinitas). 13 (4), 35–43.

PubMed Abstract | Google Scholar

Nunnari, J., and Suomalainen, A. (2012). Mitochondria: In sickness and in health. Cell 148 (6), 1145–1159. doi:10.1016/j.cell.2012.02.035

PubMed Abstract | CrossRef Full Text | Google Scholar

Prakash, Y. S., Pabelick, C. M., and Sieck, G. C. (2017). Mitochondrial dysfunction in airway disease. Chest 152 (3), 618–626. doi:10.1016/j.chest.2017.03.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Sorrentino, V., Menzies, K. J., and Auwerx, J. (2018). Repairing mitochondrial dysfunction in disease. Annu. Rev. Pharmacol. Toxicol. 58, 353–389. doi:10.1146/annurev-pharmtox-010716-104908

PubMed Abstract | CrossRef Full Text | Google Scholar

Vafai, S. B., and Mootha, V. K. (2012). Mitochondrial disorders as windows into an ancient organelle. Nature 491 (7424), 374–383. doi:10.1038/nature11707

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhong, G., Venkatesan, J. K., Madry, H., and Cucchiarini, M. (2022). Advances in human mitochondria-based therapies. Int. J. Mol. Sci. 24 (1), 608. doi:10.3390/ijms24010608

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: natural products, mitochondrial dysfunction, metabolism, oxidative stress, mitochondrial disease

Citation: Xie C, Ma L, Wang X and Xiong X (2023) Editorial: Natural products in regulating mitochondrial dysfunction. Front. Pharmacol. 14:1233718. doi: 10.3389/fphar.2023.1233718

Received: 02 June 2023; Accepted: 27 June 2023;
Published: 30 June 2023.

Edited by:

Javier Echeverria, University of Santiago, Chile

Reviewed by:

Luca Rastrelli, University of Salerno, Italy

Copyright © 2023 Xie, Ma, Wang and Xiong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Caifeng Xie, eGllY2FpZmVuZzIwMTNAMTYzLmNvbQ==

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.