Background: NADPH-oxidase-2 up-regulation has been suggested in liver damage perpetuation via an oxidative stress-mediated mechanism. n-6/n-3 polyunsaturated fatty acids ratio derangement has been reported in liver disease. Aim: To explore polyunsaturated fatty acids balance and its interplay with platelet oxidative stress in liver cirrhosis. Methods: A cross-sectional study in 51 cirrhotic patients and sex- and age-matched controls was performed. Serum polyunsaturated fatty acids and oxidative stress markers (urinary isoprostanes and serum soluble NADPH-oxidase-2-derived peptide) were measured. The effect on platelet oxidative stress of n-6/n-3 polyunsaturated fatty acids ratio in vitro and in vivo (1-week supplementation with 3 g/daily n-3-polyunsaturated fatty acids) was tested. Results: Compared to controls, cirrhotic patients had significantly higher n-6/n-3 polyunsaturated fatty acids ratio. n-6/n-3 polyunsaturated fatty acids ratio correlated significantly with disease severity and oxidative stress markers. In vitro experiments showed that in Child-Pugh C patients' platelets incubation with low n-6/n-3 polyunsaturated fatty acids ratio resulted in dose-dependent decrease of radical oxigen species (-39%), isoprostanes (-25%) and NADPH-oxidase-2 regulation (-51%). n-3 polyunsaturated fatty acids supplemented patients showed significant oxidative stress indexes reduction. Conclusions: In cirrhosis, n-6/n-3 polyunsaturated fatty acids imbalance up-regulates platelet NADPH-oxidase-2 with ensuing oxidative stress. Further study to evaluate if n-3 supplementation may reduce disease progression is warranted.

Polyunsaturated fatty acids balance affects platelet NOX2 activity in patients with liver cirrhosis / S. Basili, V. Raparelli, L. Napoleone, M. Del Ben, M. Merli, O. Riggio, C. Nocella, R. Carnevale, P. Pignatelli, F. Violi, F. Angelico, D. Amoroso, S. Bartimoccia, V.L. Burgio, C. Calabrese, A. Carboni, O. De Felice, S. Di Santo, V. Giannelli, C. Lucidi, C. Nigro, F.S. Pignataro, M. Proietti, R. Russo, G. Talerico. - In: DIGESTIVE AND LIVER DISEASE. - ISSN 1590-8658. - 46:7(2014 Jul), pp. 632-638. [10.1016/j.dld.2014.02.021]

Polyunsaturated fatty acids balance affects platelet NOX2 activity in patients with liver cirrhosis

M. Proietti
Membro del Collaboration Group
;
2014

Abstract

Background: NADPH-oxidase-2 up-regulation has been suggested in liver damage perpetuation via an oxidative stress-mediated mechanism. n-6/n-3 polyunsaturated fatty acids ratio derangement has been reported in liver disease. Aim: To explore polyunsaturated fatty acids balance and its interplay with platelet oxidative stress in liver cirrhosis. Methods: A cross-sectional study in 51 cirrhotic patients and sex- and age-matched controls was performed. Serum polyunsaturated fatty acids and oxidative stress markers (urinary isoprostanes and serum soluble NADPH-oxidase-2-derived peptide) were measured. The effect on platelet oxidative stress of n-6/n-3 polyunsaturated fatty acids ratio in vitro and in vivo (1-week supplementation with 3 g/daily n-3-polyunsaturated fatty acids) was tested. Results: Compared to controls, cirrhotic patients had significantly higher n-6/n-3 polyunsaturated fatty acids ratio. n-6/n-3 polyunsaturated fatty acids ratio correlated significantly with disease severity and oxidative stress markers. In vitro experiments showed that in Child-Pugh C patients' platelets incubation with low n-6/n-3 polyunsaturated fatty acids ratio resulted in dose-dependent decrease of radical oxigen species (-39%), isoprostanes (-25%) and NADPH-oxidase-2 regulation (-51%). n-3 polyunsaturated fatty acids supplemented patients showed significant oxidative stress indexes reduction. Conclusions: In cirrhosis, n-6/n-3 polyunsaturated fatty acids imbalance up-regulates platelet NADPH-oxidase-2 with ensuing oxidative stress. Further study to evaluate if n-3 supplementation may reduce disease progression is warranted.
isoprostanes; liver cirrhosis; diet; pufa; nadph oxidase; polyunsaturated fatty acids; oxidative stress; cirrhosis
Settore MED/09 - Medicina Interna
lug-2014
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/748202
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