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<journal-id journal-id-type="publisher-id">Front. Pharmacol.</journal-id>
<journal-title>Frontiers in Pharmacology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Pharmacol.</abbrev-journal-title>
<issn pub-type="epub">1663-9812</issn>
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<publisher-name>Frontiers Media S.A.</publisher-name>
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<article-id pub-id-type="publisher-id">1200137</article-id>
<article-id pub-id-type="doi">10.3389/fphar.2023.1200137</article-id>
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<subj-group subj-group-type="heading">
<subject>Pharmacology</subject>
<subj-group>
<subject>Editorial</subject>
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<title-group>
<article-title>Editorial: The pharmacological effects and mechanisms of drugs against human diseases by modulating redox homeostasis</article-title>
<alt-title alt-title-type="left-running-head">Zhang et al.</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fphar.2023.1200137">10.3389/fphar.2023.1200137</ext-link>
</alt-title>
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<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Zhang</surname>
<given-names>Ying</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1578891/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Shan</surname>
<given-names>Luchen</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/364585/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Yang</surname>
<given-names>Fuchun</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1942951/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Liu</surname>
<given-names>Zhihao</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/443258/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Xu</surname>
<given-names>Ming</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1937589/overview"/>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Graduate School of Medicine</institution>, <institution>Yamaguchi University</institution>, <addr-line>Yamaguchi</addr-line>, <country>Japan</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Development of Chinese Ministry of Education</institution>, <institution>Institute of New Drug Research</institution>, <institution>Jinan University College of Pharmacy</institution>, <addr-line>Guangzhou</addr-line>, <country>China</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Department of Cancer Biology</institution>, <institution>University of Cincinnati College of Medicine</institution>, <addr-line>Cincinnati</addr-line>, <addr-line>OH</addr-line>, <country>United States</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Department of Clinical Pharmacology</institution>, <institution>College of Pharmacy</institution>, <institution>Dalian Medical University</institution>, <addr-line>Dalian</addr-line>, <country>China</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/16703/overview">Filippo Drago</ext-link>, University of Catania, Italy</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1067980/overview">Holger Steinbrenner</ext-link>, Friedrich Schiller University Jena, Germany</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Luchen Shan, <email>ytysxs@126.com</email>; Fuchun Yang, <email>yangfu@ucmail.uc.edu</email>; Zhihao Liu, <email>liuzhihao12399@126.com</email>; Ming Xu, <email>mingx2003@hotmail.com</email>
</corresp>
</author-notes>
<pub-date pub-type="epub">
<day>14</day>
<month>07</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>14</volume>
<elocation-id>1200137</elocation-id>
<history>
<date date-type="received">
<day>04</day>
<month>04</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>10</day>
<month>07</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2023 Zhang, Shan, Yang, Liu and Xu.</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Zhang, Shan, Yang, Liu and Xu</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>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.</p>
</license>
</permissions>
<related-article id="RA1" related-article-type="commentary-article" journal-id="Front. Pharmacol." xlink:href="https://www.frontiersin.org/researchtopic/46488" ext-link-type="uri">Editorial on the Research Topic <article-title>The pharmacological effects and mechanisms of drugs against human diseases by modulating redox homeostasis</article-title>
</related-article>
<kwd-group>
<kwd>herbal medicine</kwd>
<kwd>redox homeostasis</kwd>
<kwd>pharmacological effects</kwd>
<kwd>reactive oxygen species</kwd>
<kwd>bioactive molecule</kwd>
</kwd-group>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Experimental Pharmacology and Drug Discovery</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<p>Redox homeostasis is a critical process in maintaining proper cell, tissue, and organ functions in the body. In the past decades, research in the field of redox homeostasis has become increasingly popular. With the advancement of science, two new concepts of oxidative eustress and oxidative distress have been proposed (<xref ref-type="bibr" rid="B11">Niki, 2016</xref>). Physiologically, a complex network of antioxidant enzymes, including superoxide dismutase, catalase, and glutathione peroxidase, plays a critical role in maintaining redox homeostasis by neutralizing ROS and preventing oxidative damage, denoted as oxidative eustress (<xref ref-type="bibr" rid="B14">Sies, 2021</xref>). On the other hand, oxidative distress which means supraphysiological oxidative challenges/damages are associated with multiple disorders, such as neurodegenerative diseases including Alzheimer&#x2019;s disease, Parkinson&#x2019;s disease, Huntington&#x2019;s disease (<xref ref-type="bibr" rid="B8">Korovesis et al., 2023</xref>); ischemia diseases (<xref ref-type="bibr" rid="B5">Chen and Li, 2020</xref>); cancers (<xref ref-type="bibr" rid="B9">Lyons et al., 2023</xref>); chronic inflammatory disorders (IBD) (<xref ref-type="bibr" rid="B1">Alemany-Cosme et al., 2021</xref>); and metabolic disorders such as diabetes and NAFLD (<xref ref-type="bibr" rid="B4">Braud et al., 2017</xref>; <xref ref-type="bibr" rid="B13">Rendra et al., 2019</xref>). Interestingly, some ROS, such as H<sub>2</sub>O<sub>2</sub>, as important cell signaling molecules may also help explain the rather limited clinical success of antioxidants (<xref ref-type="bibr" rid="B7">Forman and Zhang, 2021</xref>). Research on the pathogenic mechanisms of ROS and development of ROS-modulating drugs has been become a popular field of study in recent decades. This special Research Topic of articles is dedicated to &#x201c;The pharmacological effects and mechanisms of drugs against human diseases by modulating redox homeostasis.&#x201d; The goal is to cover the latest research on ROS signaling pathways in diseases development and drugs to treat diseases by modulating ROS levels.</p>
<p>A total of eight basic research articles and literature reviews have been published in this Research Topic. These articles cover a variety of drugs used to combat diseases by modulating redox homeostasis.</p>
<p>To continue, four articles report the role of antioxidant drugs in digestive diseases. In nonalcoholic fatty liver disease (NAFLD), a chronic advanced liver disease, ROS production increases due to the accumulation of free fatty acids in the liver (<xref ref-type="bibr" rid="B6">Delli Bovi et al., 2021</xref>). Thus, ROS plays a crucial role in the progression of NAFLD. Moreover, ROS can cause lipid peroxidation, which leads to the accumulation of toxic lipid metabolites, and in turn damages cellular membranes and organelles. Interventions to target ROS production and oxidative stress may be promising strategies for preventing and treating NAFLD. <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fphar.2023.1148814/full">Ding et al.</ext-link> reported that epigallocatechin gallate (EGCG) can alleviate liver injury, lipid accumulation, oxidative stress, hepatic steatosis, and decrease iron overload, while also inhibiting ferroptosis in a murine model of NAFLD. The authors further demonstrated that EGCG exerts protective effects against hepatic lipotoxicity by inhibiting mitochondrial ROS-mediated hepatic ferroptosis. This provided a new perspective on potential prevention and treatment strategies for NAFLD. <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fphar.2023.1157200/full">Wu et al.</ext-link> investigated the effect of bicyclol, a clinical medicine, on NAFLD. The authors conducted proteomics analyses and validation experiments, which confirmed the therapeutic effect of bicyclol on NAFLD, revealing that this effect may be linked to signaling pathways associated with bile acid metabolism, cytochrome P450-mediated metabolism, metal ion metabolism, angiogenesis, and immunological responses. On the other hand, ROS has been implicated in the pathogenesis of many intestinal diseases, including IBD, colorectal cancer, and intestinal ischemia-reperfusion (II/R) injury. <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fphar.2022.1060104/full">Li et al.</ext-link> discovered that II/R could induce an inflammatory response and oxidative stress, which subsequently activated the NOD-, LRR-, and pyrin domain-containing 3 (NLRP3) inflammasome and caused damage to intestinal and lung tissue. However, these pathological effects were significantly attenuated by Corilagin (Cor). The authors further demonstrated that Cor may inhibit ROS-induced NLRP3 inflammasome activation and pyroptosis both <italic>in vivo</italic> and <italic>in vitro</italic>, suggesting the potential therapeutic benefits of Cor in mitigating II/R-induced tissue injury. <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fphar.2023.1127931/full">Arenbaoligao et al.</ext-link> demonstrated that Kumatakenin, a Chinese medicine, can protect against IBD-induced epithelial ferroptosis injury in colonic tissues. Using RNA sequencing and molecular docking methods, the authors verified that Kumatakenin suppresses IBD-induced epithelial ferroptosis by modulating the Eno3-iron regulatory protein axis. These findings provide a scientific rationale for the clinical application of Kumatakenin in the treatment of colitis.</p>
<p>Apart from treating diseases through antioxidant signal pathways, other drugs were designed to increase ROS levels in specific parts of the body, such as anti-cancer, anti-<italic>Escherichia coli</italic> (<italic>E. coli</italic>) bacteria and protective autophagy. Several studies have reported that antioxidant approaches can indeed be used to prevent carcinogenesis (<xref ref-type="bibr" rid="B2">Amstad et al., 1990</xref>; <xref ref-type="bibr" rid="B12">Ray and Husain, 2002</xref>). On the other hand, since cancer cells are more sensitive to oxidative stress than normal cells, some ROS-inducing chemicals are used to treat established tumors (<xref ref-type="bibr" rid="B15">Wang et al., 2021</xref>). <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fphar.2022.1054803/full">Li et al.</ext-link> reported on the anti-cancer effect of <italic>Sanguisorba officinalis</italic> L. (SOL). The authors demonstrated that SOL could increase ROS levels and inhibit the proliferation, migration, and invasion of non-small cell lung cancer cells. Ebselen, a glutathione peroxidase mimic has been confirmed to reduce ROS levels by neutralizing H<sub>2</sub>O<sub>2</sub> (<xref ref-type="bibr" rid="B10">Nakamura et al., 2002</xref>). However, Ebselen can also increase ROS level with a high concentration in yeast cells (<xref ref-type="bibr" rid="B3">Azad et al., 2014</xref>). In this Research Topic, <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fphar.2022.1080281/full">Chen et al.</ext-link> reported on the synergistic anti-bacterial effect of the combination of SBC3 and Ebselen against <italic>E. coli</italic> and other difficult-to-treat Gram-negative bacteria, achieved by increasing ROS levels through the ROS pathway. These two articles provide new perspectives on the potential use of drugs for disease treatment by regulating ROS levels.</p>
<p>In summary, this Research Topic focused on the regulation of oxidative homeostasis as a potential strategy for treating diseases. The information gained from this Research Topic may help identify new biomolecules for disease treatment and drive the development of novel therapeutic drugs.</p>
</body>
<back>
<sec id="s1">
<title>Author contributions</title>
<p>YZ and MX prepared the manuscript, LS, ZL, and FY edited the manuscript.</p>
</sec>
<ack>
<p>We want to express our appreciation to all of authors who contributed to this Research Topic. As Guest-Editors, we are thankful for the substantial input from each author, which helped ensure the success of this Research Topic. We would also like to extend our gratitude to the reviewers for their valuable constructive comments and suggestions. Lastly, we would like to give a special acknowledgement to the members of the Frontiers Editorial Office for their assistance in making this work a triumph.</p>
</ack>
<sec sec-type="COI-statement" id="s2">
<title>Conflict of interest</title>
<p>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.</p>
</sec>
<sec sec-type="disclaimer" id="s3">
<title>Publisher&#x2019;s note</title>
<p>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.</p>
</sec>
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