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Lipophilic antioxidants prevent lipopolysaccharide-induced mitochondrial dysfunction through mitochondrial biogenesis improvement

  • Pedro Bullón
  • , Lourdes Román-Malo
  • , Fabiola Marín-Aguilar
  • , José Miguel Alvarez-Suarez
  • , Francesca Giampieri
  • , Maurizio Battino*
  • , Mario D. Cordero
  • *Corresponding author for this work
  • Universidad de Sevilla
  • Universita Politecnica Delle Marche
  • Universidad Internacional Iberoamericana (UNINI)
  • Universidad Nacional de Chimborazo
  • Universidad Europea Del Atlántico (UEA)

Research output: Contribution to journalArticlepeer-review

64 Scopus citations

Abstract

Oxidative stress is implicated in several infectious diseases. In this regard, lipopolysaccharide (LPS), an endotoxic component, induces mitochondrial dysfunction and oxidative stress in several pathological events such as periodontal disease or sepsis. In our experiments, LPS-treated fibroblasts provoked increased oxidative stress, mitochondrial dysfunction, reduced oxygen consumption and mitochondrial biogenesis. After comparing coenzyme Q10 (CoQ10) and N-acetylcysteine (NAC), we observed a more significant protection of CoQ10 than of NAC, which was comparable with other lipophilic and hydrophilic antioxidants such as vitamin E or BHA respectively. CoQ10 improved mitochondrial biogenesis by activating PGC-1α and TFAM. This lipophilic antioxidant protection was observed in mice after LPS injection. These results show that mitochondria-targeted lipophilic antioxidants could be a possible specific therapeutic strategy in pharmacology in the treatment of infectious diseases and their complications.

Original languageEnglish
Pages (from-to)1-8
Number of pages8
JournalPharmacological Research
Volume91
DOIs
StatePublished - Jan 2015
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Coenzyme Q
  • Lipopolysaccharide
  • Mitochondria
  • N-acetylcysteine
  • Porphyromonas gingivalis

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