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Linked Open Data
β-RA reduces DMQ/CoQ ratio and rescues the encephalopathic phenotype in Coq9R239X mice.
Identificadores del recurso
http://hdl.handle.net/10668/13248
30482867
10.15252/emmm.201809466
1757-4684
PMC6328940
https://doi.org/10.15252/emmm.201809466
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328940/pdf
Procedència
(RISalud-ANDALUCÍA)

Fitxa

Títol:
β-RA reduces DMQ/CoQ ratio and rescues the encephalopathic phenotype in Coq9R239X mice.
Tema:
2,4‐dihydroxybenzoic acid
Q synthome
astrogliosis
mitochondrial encephalopathy
spongiosis
Animals
Brain
Disease Models, Animal
Energy Metabolism
Histocytochemistry
Hydroxybenzoates
Mice
Mitochondrial Encephalomyopathies
Neuroprotective Agents
Salicylic Acid
Survival Analysis
Treatment Outcome
Ubiquinone
Descripció:
Coenzyme Q (CoQ) deficiency has been associated with primary defects in the CoQ biosynthetic pathway or to secondary events. In some cases, the exogenous CoQ supplementation has limited efficacy. In the Coq9R239X mouse model with fatal mitochondrial encephalopathy due to CoQ deficiency, we have tested the therapeutic potential of β-resorcylic acid (β-RA), a structural analog of the CoQ precursor 4-hydroxybenzoic acid and the anti-inflammatory salicylic acid. β-RA noticeably rescued the phenotypic, morphological, and histopathological signs of the encephalopathy, leading to a significant increase in the survival. Those effects were due to the decrease of the levels of demethoxyubiquinone-9 (DMQ9) and the increase of mitochondrial bioenergetics in peripheral tissues. However, neither CoQ biosynthesis nor mitochondrial function changed in the brain after the therapy, suggesting that some endocrine interactions may induce the reduction of the astrogliosis, spongiosis, and the secondary down-regulation of astrocytes-related neuroinflammatory genes. Because the therapeutic outcomes of β-RA administration were superior to those after CoQ10 supplementation, its use in the clinic should be considered in CoQ deficiencies.
Idioma:
Autor/Productor:
Hidalgo-Gutierrez, Agustín
Barriocanal-Casado, Eliana
Bakkali, Mohammed
Diaz-Casado, M Elena
Sanchez-Maldonado, Laura
Romero, Miguel
Sayed, Ramy K
Prehn, Cornelia
Escames, Germaine
Duarte, Juan
Acuña-Castroviejo, Darío
Lopez, Luis C
Drets:
Attribution 4.0 International
http://creativecommons.org/licenses/by/4.0/
open access
Data:
2023-01-25T10:25:16Z
2019
Tipo de recurso:
research article
VoR
Format:
application/pdf

oai_dc

Descarregar XML

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    1. <dc:title>β-RA reduces DMQ/CoQ ratio and rescues the encephalopathic phenotype in Coq9R239X mice.</dc:title>

    2. <dc:creator>Hidalgo-Gutierrez, Agustín</dc:creator>

    3. <dc:creator>Barriocanal-Casado, Eliana</dc:creator>

    4. <dc:creator>Bakkali, Mohammed</dc:creator>

    5. <dc:creator>Diaz-Casado, M Elena</dc:creator>

    6. <dc:creator>Sanchez-Maldonado, Laura</dc:creator>

    7. <dc:creator>Romero, Miguel</dc:creator>

    8. <dc:creator>Sayed, Ramy K</dc:creator>

    9. <dc:creator>Prehn, Cornelia</dc:creator>

    10. <dc:creator>Escames, Germaine</dc:creator>

    11. <dc:creator>Duarte, Juan</dc:creator>

    12. <dc:creator>Acuña-Castroviejo, Darío</dc:creator>

    13. <dc:creator>Lopez, Luis C</dc:creator>

    14. <dc:subject>2,4‐dihydroxybenzoic acid</dc:subject>

    15. <dc:subject>Q synthome</dc:subject>

    16. <dc:subject>astrogliosis</dc:subject>

    17. <dc:subject>mitochondrial encephalopathy</dc:subject>

    18. <dc:subject>spongiosis</dc:subject>

    19. <dc:subject>Animals</dc:subject>

    20. <dc:subject>Brain</dc:subject>

    21. <dc:subject>Disease Models, Animal</dc:subject>

    22. <dc:subject>Energy Metabolism</dc:subject>

    23. <dc:subject>Histocytochemistry</dc:subject>

    24. <dc:subject>Hydroxybenzoates</dc:subject>

    25. <dc:subject>Mice</dc:subject>

    26. <dc:subject>Mitochondrial Encephalomyopathies</dc:subject>

    27. <dc:subject>Neuroprotective Agents</dc:subject>

    28. <dc:subject>Salicylic Acid</dc:subject>

    29. <dc:subject>Survival Analysis</dc:subject>

    30. <dc:subject>Treatment Outcome</dc:subject>

    31. <dc:subject>Ubiquinone</dc:subject>

    32. <dc:description>Coenzyme Q (CoQ) deficiency has been associated with primary defects in the CoQ biosynthetic pathway or to secondary events. In some cases, the exogenous CoQ supplementation has limited efficacy. In the Coq9R239X mouse model with fatal mitochondrial encephalopathy due to CoQ deficiency, we have tested the therapeutic potential of β-resorcylic acid (β-RA), a structural analog of the CoQ precursor 4-hydroxybenzoic acid and the anti-inflammatory salicylic acid. β-RA noticeably rescued the phenotypic, morphological, and histopathological signs of the encephalopathy, leading to a significant increase in the survival. Those effects were due to the decrease of the levels of demethoxyubiquinone-9 (DMQ9) and the increase of mitochondrial bioenergetics in peripheral tissues. However, neither CoQ biosynthesis nor mitochondrial function changed in the brain after the therapy, suggesting that some endocrine interactions may induce the reduction of the astrogliosis, spongiosis, and the secondary down-regulation of astrocytes-related neuroinflammatory genes. Because the therapeutic outcomes of β-RA administration were superior to those after CoQ10 supplementation, its use in the clinic should be considered in CoQ deficiencies.</dc:description>

    33. <dc:date>2023-01-25T10:25:16Z</dc:date>

    34. <dc:date>2023-01-25T10:25:16Z</dc:date>

    35. <dc:date>2019</dc:date>

    36. <dc:type>research article</dc:type>

    37. <dc:type>VoR</dc:type>

    38. <dc:identifier>http://hdl.handle.net/10668/13248</dc:identifier>

    39. <dc:identifier>30482867</dc:identifier>

    40. <dc:identifier>10.15252/emmm.201809466</dc:identifier>

    41. <dc:identifier>1757-4684</dc:identifier>

    42. <dc:identifier>PMC6328940</dc:identifier>

    43. <dc:identifier>https://doi.org/10.15252/emmm.201809466</dc:identifier>

    44. <dc:identifier>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328940/pdf</dc:identifier>

    45. <dc:language>en</dc:language>

    46. <dc:rights>Attribution 4.0 International</dc:rights>

    47. <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>

    48. <dc:rights>open access</dc:rights>

    49. <dc:format>application/pdf</dc:format>

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