| Literature DB >> 25447593 |
Pedro Bullón1, Lourdes Román-Malo2, Fabiola Marín-Aguilar2, José Miguel Alvarez-Suarez3, Francesca Giampieri4, Maurizio Battino5, Mario D Cordero6.
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.Entities:
Keywords: Coenzyme Q(10); Lipopolysaccharide; Mitochondria; N-acetylcysteine; Porphyromonas gingivalis
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Year: 2014 PMID: 25447593 DOI: 10.1016/j.phrs.2014.10.007
Source DB: PubMed Journal: Pharmacol Res ISSN: 1043-6618 Impact factor: 7.658