The idebenone metabolite QS10 restores electron transfer in complex I and coenzyme Q defects
Idebenone is a hydrophilic short-chain coenzyme (Co) Q analogue, which has been used as a potential bypass of defective complex I in both Leber Hereditary Optic Neuropathy and OPA1-dependent Dominant Optic Atrophy. Based on its potential antioxidant effects, it has also been tested in degenerative d...
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creator | Giorgio, Valentina Schiavone, Marco Galber, Chiara Carini, Marco Da Ros, Tatiana Petronilli, Valeria Argenton, Francesco Carelli, Valerio Acosta Lopez, Manuel J. Salviati, Leonardo Prato, Maurizio Bernardi, Paolo |
description | Idebenone is a hydrophilic short-chain coenzyme (Co) Q analogue, which has been used as a potential bypass of defective complex I in both Leber Hereditary Optic Neuropathy and OPA1-dependent Dominant Optic Atrophy. Based on its potential antioxidant effects, it has also been tested in degenerative disorders such as Friedreich's ataxia, Huntington's and Alzheimer's diseases. Idebenone is rapidly modified but the biological effects of its metabolites have been characterized only partially. Here we have studied the effects of quinones generated during in vivo metabolism of idebenone with specific emphasis on 6-(9-carboxynonyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone (QS10). QS10 partially restored respiration in cells deficient of complex I or of CoQ without inducing the mitochondrial permeability transition, a detrimental effect of idebenone that may offset its potential benefits [Giorgio et al. (2012) Biochim. Biophys. Acta 1817: 363–369]. Remarkably, respiration was largely rotenone-insensitive in complex I deficient cells and rotenone-sensitive in CoQ deficient cells. These findings indicate that, like idebenone, QS10 can provide a bypass to defective complex I; and that, unlike idebenone, QS10 can partially replace endogenous CoQ. In zebrafish (Danio rerio) treated with rotenone, QS10 was more effective than idebenone in allowing partial recovery of respiration (to 40% and 20% of the basal respiration of untreated embryos, respectively) and allowing zebrafish survival (80% surviving embryos at 60 h post-fertilization, a time point at which all rotenone-treated embryos otherwise died). We conclude that QS10 is potentially more active than idebenone in the treatment of diseases caused by complex I defects, and that it could also be used in CoQ deficiencies of genetic and acquired origin.
[Display omitted]
•Idebenone is a short-chain quinone used to bypass defective mitochondrial complex I.•The QS10 metabolite can partially replace endogenous coenzyme Q but also mediate electron transfer in the presence of rotenone.•QS10 but not idebenone rescues zebrafish from rotenone toxicity. |
doi_str_mv | 10.1016/j.bbabio.2018.04.006 |
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[Display omitted]
•Idebenone is a short-chain quinone used to bypass defective mitochondrial complex I.•The QS10 metabolite can partially replace endogenous coenzyme Q but also mediate electron transfer in the presence of rotenone.•QS10 but not idebenone rescues zebrafish from rotenone toxicity.</description><identifier>ISSN: 0005-2728</identifier><identifier>EISSN: 1879-2650</identifier><identifier>DOI: 10.1016/j.bbabio.2018.04.006</identifier><identifier>PMID: 29694828</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adenosine Triphosphate - metabolism ; Animals ; Antioxidants - chemistry ; Antioxidants - pharmacology ; Ataxia - metabolism ; Ataxia - pathology ; Cell Respiration ; Cells, Cultured ; Complex I ; Electron transfer ; Electron Transport ; Electron Transport Complex I - deficiency ; Electron Transport Complex I - metabolism ; Embryo, Nonmammalian - cytology ; Embryo, Nonmammalian - drug effects ; Embryo, Nonmammalian - metabolism ; Idebenone ; Mice ; Mitochondria, Liver - drug effects ; Mitochondria, Liver - metabolism ; Mitochondrial Diseases - metabolism ; Mitochondrial Diseases - pathology ; Muscle Weakness - metabolism ; Muscle Weakness - pathology ; Respiration ; Ubiquinone ; Ubiquinone - analogs & derivatives ; Ubiquinone - chemistry ; Ubiquinone - deficiency ; Ubiquinone - metabolism ; Ubiquinone - pharmacology ; Zebrafish - embryology ; Zebrafish - metabolism</subject><ispartof>Biochimica et biophysica acta. Bioenergetics, 2018-09, Vol.1859 (9), p.901-908</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-1c6765874ebd2e89fa564a765101b682e09796880aa806119cdd9f69d2c4a4173</citedby><cites>FETCH-LOGICAL-c434t-1c6765874ebd2e89fa564a765101b682e09796880aa806119cdd9f69d2c4a4173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S000527281830080X$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29694828$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Giorgio, Valentina</creatorcontrib><creatorcontrib>Schiavone, Marco</creatorcontrib><creatorcontrib>Galber, Chiara</creatorcontrib><creatorcontrib>Carini, Marco</creatorcontrib><creatorcontrib>Da Ros, Tatiana</creatorcontrib><creatorcontrib>Petronilli, Valeria</creatorcontrib><creatorcontrib>Argenton, Francesco</creatorcontrib><creatorcontrib>Carelli, Valerio</creatorcontrib><creatorcontrib>Acosta Lopez, Manuel J.</creatorcontrib><creatorcontrib>Salviati, Leonardo</creatorcontrib><creatorcontrib>Prato, Maurizio</creatorcontrib><creatorcontrib>Bernardi, Paolo</creatorcontrib><title>The idebenone metabolite QS10 restores electron transfer in complex I and coenzyme Q defects</title><title>Biochimica et biophysica acta. Bioenergetics</title><addtitle>Biochim Biophys Acta Bioenerg</addtitle><description>Idebenone is a hydrophilic short-chain coenzyme (Co) Q analogue, which has been used as a potential bypass of defective complex I in both Leber Hereditary Optic Neuropathy and OPA1-dependent Dominant Optic Atrophy. Based on its potential antioxidant effects, it has also been tested in degenerative disorders such as Friedreich's ataxia, Huntington's and Alzheimer's diseases. Idebenone is rapidly modified but the biological effects of its metabolites have been characterized only partially. Here we have studied the effects of quinones generated during in vivo metabolism of idebenone with specific emphasis on 6-(9-carboxynonyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone (QS10). QS10 partially restored respiration in cells deficient of complex I or of CoQ without inducing the mitochondrial permeability transition, a detrimental effect of idebenone that may offset its potential benefits [Giorgio et al. (2012) Biochim. Biophys. Acta 1817: 363–369]. Remarkably, respiration was largely rotenone-insensitive in complex I deficient cells and rotenone-sensitive in CoQ deficient cells. These findings indicate that, like idebenone, QS10 can provide a bypass to defective complex I; and that, unlike idebenone, QS10 can partially replace endogenous CoQ. In zebrafish (Danio rerio) treated with rotenone, QS10 was more effective than idebenone in allowing partial recovery of respiration (to 40% and 20% of the basal respiration of untreated embryos, respectively) and allowing zebrafish survival (80% surviving embryos at 60 h post-fertilization, a time point at which all rotenone-treated embryos otherwise died). We conclude that QS10 is potentially more active than idebenone in the treatment of diseases caused by complex I defects, and that it could also be used in CoQ deficiencies of genetic and acquired origin.
[Display omitted]
•Idebenone is a short-chain quinone used to bypass defective mitochondrial complex I.•The QS10 metabolite can partially replace endogenous coenzyme Q but also mediate electron transfer in the presence of rotenone.•QS10 but not idebenone rescues zebrafish from rotenone toxicity.</description><subject>Adenosine Triphosphate - metabolism</subject><subject>Animals</subject><subject>Antioxidants - chemistry</subject><subject>Antioxidants - pharmacology</subject><subject>Ataxia - metabolism</subject><subject>Ataxia - pathology</subject><subject>Cell Respiration</subject><subject>Cells, Cultured</subject><subject>Complex I</subject><subject>Electron transfer</subject><subject>Electron Transport</subject><subject>Electron Transport Complex I - deficiency</subject><subject>Electron Transport Complex I - metabolism</subject><subject>Embryo, Nonmammalian - cytology</subject><subject>Embryo, Nonmammalian - drug effects</subject><subject>Embryo, Nonmammalian - metabolism</subject><subject>Idebenone</subject><subject>Mice</subject><subject>Mitochondria, Liver - drug effects</subject><subject>Mitochondria, Liver - metabolism</subject><subject>Mitochondrial Diseases - metabolism</subject><subject>Mitochondrial Diseases - pathology</subject><subject>Muscle Weakness - metabolism</subject><subject>Muscle Weakness - pathology</subject><subject>Respiration</subject><subject>Ubiquinone</subject><subject>Ubiquinone - analogs & derivatives</subject><subject>Ubiquinone - chemistry</subject><subject>Ubiquinone - deficiency</subject><subject>Ubiquinone - metabolism</subject><subject>Ubiquinone - pharmacology</subject><subject>Zebrafish - embryology</subject><subject>Zebrafish - metabolism</subject><issn>0005-2728</issn><issn>1879-2650</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kFFLHDEQx4NYvNP6DUTy6MtuJ7lcNnkRRGx7IJRS-1YI2WQWc-wmZ7JXaj99I6c-9iUhw--fmfkRcsGgZcDkp23b97YPqeXAVAuiBZBHZMlUpxsu13BMlgCwbnjH1YKclrKFGhN8dUIWXEstFFdL8uvhEWnw2GNMEemEs-3TGGak338woBnLnOpBcUQ35xTpnG0sA2YaInVp2o34h26ojb6-MP59nmqSehwqXj6SD4MdC56_3mfk5-e7h9uvzf23L5vbm_vGiZWYG-ZkJ9eqE9h7jkoPdi2FraW6Zy8VR9CdlkqBtQokY9p5rwepPXfCCtatzsjV4d9dTk_7OrKZQnE4jjZi2hfDYcUEZ1rIiooD6nIqJeNgdjlMNj8bBubFq9mag1fz4tWAMNVrjV2-dtj3E_r30JvIClwfAKx7_g6YTXEBo0MfclVhfAr_7_APyJeJ0w</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Giorgio, Valentina</creator><creator>Schiavone, Marco</creator><creator>Galber, Chiara</creator><creator>Carini, Marco</creator><creator>Da Ros, Tatiana</creator><creator>Petronilli, Valeria</creator><creator>Argenton, Francesco</creator><creator>Carelli, Valerio</creator><creator>Acosta Lopez, Manuel J.</creator><creator>Salviati, Leonardo</creator><creator>Prato, Maurizio</creator><creator>Bernardi, Paolo</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20180901</creationdate><title>The idebenone metabolite QS10 restores electron transfer in complex I and coenzyme Q defects</title><author>Giorgio, Valentina ; Schiavone, Marco ; Galber, Chiara ; Carini, Marco ; Da Ros, Tatiana ; Petronilli, Valeria ; Argenton, Francesco ; Carelli, Valerio ; Acosta Lopez, Manuel J. ; Salviati, Leonardo ; Prato, Maurizio ; Bernardi, Paolo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-1c6765874ebd2e89fa564a765101b682e09796880aa806119cdd9f69d2c4a4173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adenosine Triphosphate - metabolism</topic><topic>Animals</topic><topic>Antioxidants - chemistry</topic><topic>Antioxidants - pharmacology</topic><topic>Ataxia - metabolism</topic><topic>Ataxia - pathology</topic><topic>Cell Respiration</topic><topic>Cells, Cultured</topic><topic>Complex I</topic><topic>Electron transfer</topic><topic>Electron Transport</topic><topic>Electron Transport Complex I - deficiency</topic><topic>Electron Transport Complex I - metabolism</topic><topic>Embryo, Nonmammalian - cytology</topic><topic>Embryo, Nonmammalian - drug effects</topic><topic>Embryo, Nonmammalian - metabolism</topic><topic>Idebenone</topic><topic>Mice</topic><topic>Mitochondria, Liver - drug effects</topic><topic>Mitochondria, Liver - metabolism</topic><topic>Mitochondrial Diseases - metabolism</topic><topic>Mitochondrial Diseases - pathology</topic><topic>Muscle Weakness - metabolism</topic><topic>Muscle Weakness - pathology</topic><topic>Respiration</topic><topic>Ubiquinone</topic><topic>Ubiquinone - analogs & derivatives</topic><topic>Ubiquinone - chemistry</topic><topic>Ubiquinone - deficiency</topic><topic>Ubiquinone - metabolism</topic><topic>Ubiquinone - pharmacology</topic><topic>Zebrafish - embryology</topic><topic>Zebrafish - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Giorgio, Valentina</creatorcontrib><creatorcontrib>Schiavone, Marco</creatorcontrib><creatorcontrib>Galber, Chiara</creatorcontrib><creatorcontrib>Carini, Marco</creatorcontrib><creatorcontrib>Da Ros, Tatiana</creatorcontrib><creatorcontrib>Petronilli, Valeria</creatorcontrib><creatorcontrib>Argenton, Francesco</creatorcontrib><creatorcontrib>Carelli, Valerio</creatorcontrib><creatorcontrib>Acosta Lopez, Manuel J.</creatorcontrib><creatorcontrib>Salviati, Leonardo</creatorcontrib><creatorcontrib>Prato, Maurizio</creatorcontrib><creatorcontrib>Bernardi, Paolo</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochimica et biophysica acta. Bioenergetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Giorgio, Valentina</au><au>Schiavone, Marco</au><au>Galber, Chiara</au><au>Carini, Marco</au><au>Da Ros, Tatiana</au><au>Petronilli, Valeria</au><au>Argenton, Francesco</au><au>Carelli, Valerio</au><au>Acosta Lopez, Manuel J.</au><au>Salviati, Leonardo</au><au>Prato, Maurizio</au><au>Bernardi, Paolo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The idebenone metabolite QS10 restores electron transfer in complex I and coenzyme Q defects</atitle><jtitle>Biochimica et biophysica acta. Bioenergetics</jtitle><addtitle>Biochim Biophys Acta Bioenerg</addtitle><date>2018-09-01</date><risdate>2018</risdate><volume>1859</volume><issue>9</issue><spage>901</spage><epage>908</epage><pages>901-908</pages><issn>0005-2728</issn><eissn>1879-2650</eissn><abstract>Idebenone is a hydrophilic short-chain coenzyme (Co) Q analogue, which has been used as a potential bypass of defective complex I in both Leber Hereditary Optic Neuropathy and OPA1-dependent Dominant Optic Atrophy. Based on its potential antioxidant effects, it has also been tested in degenerative disorders such as Friedreich's ataxia, Huntington's and Alzheimer's diseases. Idebenone is rapidly modified but the biological effects of its metabolites have been characterized only partially. Here we have studied the effects of quinones generated during in vivo metabolism of idebenone with specific emphasis on 6-(9-carboxynonyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone (QS10). QS10 partially restored respiration in cells deficient of complex I or of CoQ without inducing the mitochondrial permeability transition, a detrimental effect of idebenone that may offset its potential benefits [Giorgio et al. (2012) Biochim. Biophys. Acta 1817: 363–369]. Remarkably, respiration was largely rotenone-insensitive in complex I deficient cells and rotenone-sensitive in CoQ deficient cells. These findings indicate that, like idebenone, QS10 can provide a bypass to defective complex I; and that, unlike idebenone, QS10 can partially replace endogenous CoQ. In zebrafish (Danio rerio) treated with rotenone, QS10 was more effective than idebenone in allowing partial recovery of respiration (to 40% and 20% of the basal respiration of untreated embryos, respectively) and allowing zebrafish survival (80% surviving embryos at 60 h post-fertilization, a time point at which all rotenone-treated embryos otherwise died). We conclude that QS10 is potentially more active than idebenone in the treatment of diseases caused by complex I defects, and that it could also be used in CoQ deficiencies of genetic and acquired origin.
[Display omitted]
•Idebenone is a short-chain quinone used to bypass defective mitochondrial complex I.•The QS10 metabolite can partially replace endogenous coenzyme Q but also mediate electron transfer in the presence of rotenone.•QS10 but not idebenone rescues zebrafish from rotenone toxicity.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>29694828</pmid><doi>10.1016/j.bbabio.2018.04.006</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine Triphosphate - metabolism Animals Antioxidants - chemistry Antioxidants - pharmacology Ataxia - metabolism Ataxia - pathology Cell Respiration Cells, Cultured Complex I Electron transfer Electron Transport Electron Transport Complex I - deficiency Electron Transport Complex I - metabolism Embryo, Nonmammalian - cytology Embryo, Nonmammalian - drug effects Embryo, Nonmammalian - metabolism Idebenone Mice Mitochondria, Liver - drug effects Mitochondria, Liver - metabolism Mitochondrial Diseases - metabolism Mitochondrial Diseases - pathology Muscle Weakness - metabolism Muscle Weakness - pathology Respiration Ubiquinone Ubiquinone - analogs & derivatives Ubiquinone - chemistry Ubiquinone - deficiency Ubiquinone - metabolism Ubiquinone - pharmacology Zebrafish - embryology Zebrafish - metabolism |
title | The idebenone metabolite QS10 restores electron transfer in complex I and coenzyme Q defects |
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