http://www.cnr.it/ontology/cnr/individuo/prodotto/ID12838
Mitochondrial dysfunction in rat with nonalcoholic fatty liver Involvement of complex I, reactive oxygen species and cardiolipin (Articolo in rivista)
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- Label
- Mitochondrial dysfunction in rat with nonalcoholic fatty liver Involvement of complex I, reactive oxygen species and cardiolipin (Articolo in rivista) (literal)
- Anno
- 2007-01-01T00:00:00+01:00 (literal)
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- Petrosillo G; Portincasa P; Grattagliano I; Casanova G; Matera M; Ruggiero FM; Ferri D; Paradies G. (literal)
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- Rivista
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Department of Biochemistry and Molecular Biology and CNR Institute of Biomembranes and Bioenergetics, University of Bari, Bari, Italy
Section of Internal Medicine, Department of Internal and Public Medicine, University of Bari, Bari, Italy
Department of Zoology, Laboratory of Histology and Comparative Anatomy, University of Bari, Bari, Italy (literal)
- Titolo
- Mitochondrial dysfunction in rat with nonalcoholic fatty liver Involvement of complex I, reactive oxygen species and cardiolipin (literal)
- Abstract
- Mitochondrial dysfunction and oxidative stress play a central role in the pathophysiology of nonalcoholic fatty liver disease (NAFLD). This study
aimed to elucidate the mechanism(s) responsible for mitochondrial dysfunction in nonalcoholic fatty liver. Fatty liver was induced in rats with a
choline-deficient (CD) diet for 30 days.We examined the effect of CD diet on various parameters related to mitochondrial function such as complex I
activity, oxygen consumption, reactive oxygen species (ROS) generation and cardiolipin content and oxidation. The activity of complex I was
reduced by 35% in mitochondria isolated from CD livers compared with the controls. These changes in complex I activity were associated with
parallel changes in state 3 respiration. Hydrogen peroxide (H2O2) generation was significantly increased in mitochondria isolated fromCDlivers. The
mitochondrial content of cardiolipin, a phospholipid required for optimal activity of complex I, decreased by 38% as function of CD diet, while there
was a significantly increase in the level of peroxidized cardiolipin. The lower complex I activity in mitochondria from CD livers could be completely
restored to the level of control livers by exogenously added cardiolipin. This effect of cardiolipin could not be replaced by other phospholipids nor by
peroxidized cardiolipin. It is concluded that CD diet causes mitochondrial complex I dysfunction which can be attributed to ROS-induced cardiolipin
oxidation. These findings provide new insights into the alterations underlying mitochondrial dysfunction in NAFLD. (literal)
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