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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Veröffentlicht in:Biochimica et biophysica acta. Bioenergetics 2018-09, Vol.1859 (9), p.901-908
Hauptverfasser: 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
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container_issue 9
container_start_page 901
container_title Biochimica et biophysica acta. Bioenergetics
container_volume 1859
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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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. 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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 &amp; 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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 &amp; 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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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