Oxidative stress-related parameters in the liver of non-alcoholic fatty liver disease patients
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2004-03Metadata
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Videla Cabrera, Luis
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Oxidative stress-related parameters in the liver of non-alcoholic fatty liver disease patients
Author
- Videla Cabrera, Luis;
- Rodrigo Salinas, Ramón;
- Orellana Bown, Myriam;
- Fernandez, Virginia;
- Tapia Opazo, Gladys;
- Quiñones Sepúlveda, Luis;
- Varela Figueroa, Nelson;
- Contreras, Jorge;
- Lazarte, Raúl;
- Csendes Juhasz, Attila;
- Rojas Caro, Jorge;
- Maluenda, Fernando;
- Burdiles Pinto, Patricio;
- Díaz Jeraldo, Juan;
- Smok Sahid, Gladys;
- Thielemann, Lilian;
- Poniachik Teller, Jaime;
Abstract
Oxidative stress is implicated in the pathogenesis of non-alcoholic fatty liver disease (NAFLD).
In the present study, hepatic and plasma oxidative stress-related parameters were measured and
correlated with clinical and histological findings in 31 NAFLD patients showing increased bodymass
index. Liver protein carbonyl content was enhanced by 403% in patients with steatosis (n=15)
compared with control values (n=12), whereas glutathione content, superoxide dismutase (SOD)
activity and the ferric reducing ability of plasma (FRAP) were decreased by 57 %, 48% and 21%
(P<0.05) respectively. No changes in microsomal p-nitrophenol hydroxylation and the total
content of cytochrome P450 (CYP) or CYP2E1 were observed. Patients with steatohepatitis
(n=16) exhibited protein carbonyl content comparable with that of controls, whereas glutathione
content, SOD and catalase activities were decreased by 27%, 64% and 48% (P<0.05). In
addition, FRAP values in patients with steatohepatitis were reduced by 33% and 15% (P<0.05)
when compared with controls and patients with steatosis respectively, whereas p-nitrophenol
hydroxylation (52 %) and CYP2E1 content (142 %) were significantly increased (P<0.05) compared
with controls. It is concluded that oxidative stress is developed in the liver of NAFLD patients with
steatosis and is exacerbated further in patients with steatohepatitis, which is associated
with CYP2E1 induction. Substantial protein oxidation is followed by proteolysis of the modified
proteins, which may explain the co-existence of a diminished antioxidant capacity and protein
oxidation in the liver of patients with steatohepatitis.
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Clinical Science (2004) 106, 261–268 (Printed in Great Britain)
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