Paraoxonase-1 is associated with oxidative stress, fibrosis and FAS expression in chronic liver diseases

被引:81
作者
Ferre, Natalia
Marsillach, Judit
Camps, Jordi
Mackness, Bharti
Mackness, Michael
Riu, Francesc
Blai, C.
Tous, Monica
Joven, Jorge
机构
[1] Hosp Clin Univ, IDIBAPS, DNA Unit, Ctr Diagnost Biomed, E-08036 Barcelona, Spain
[2] Hosp Univ Sant Joan, Ctr Recerca Biomed, Inst Recerca Ciencies Salut, Reus 43201, Spain
[3] Manchester Royal Infirm, Dept Med, Manchester M13 9WL, Lancs, England
关键词
apoptosis; FAS; lipid peroxidation; liver disease; paraoxonases;
D O I
10.1016/j.jhep.2005.12.018
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: We previously reported that paraoxonase-1 activity measurement may be useful for the evaluation of liver diseases. Because oxidative stress plays a role in liver apoptosis, and lipid peroxides are hydrolyzed by paraoxonase-1, we have extended our studies to explore the relationships between this enzyme and oxidative stress, fibrosis and apoptosis. Methods: We measured paraoxonase-1 activity and concentration, soluble FAS concentration, serum fibrosis markers, and total peroxides in a group of patients with minimal hepatic changes (n = 25), chronic hepatitis (n = 51), or liver cirrhosis (n = 17). We also measured the Knodell activity index in liver biopsies and performed FAS and PON1 immunostaining. Results: Patients with liver diseases showed an increase in soluble FAS, fibrosis markers and paraoxonase-1 concentrations, as well as a decrease in PON1 activity. Paroxonase-1 activity and concentration were correlated with soluble FAS (r = -0.43, P < 0.001 and r = 0.27, P = 0.007, respectively). Paraoxonase-1 concentration showed a significant inverse association with FAS immunostaining (P = 0.013) and a direct association with PON1 immunostaining (P < 0.001). Conclusions: These results suggest an active role of PON1 in the regulation of oxidative stress, fibrosis and hepatic cell apoptosis in chronic liver diseases. (c) 2006 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:51 / 59
页数:9
相关论文
共 45 条
[1]   Human serum paraoxonase (PON 1) is inactivated by oxidized low density lipoprotein and preserved by antioxidants [J].
Aviram, M ;
Rosenblat, M ;
Billecke, S ;
Erogul, J ;
Sorenson, R ;
Bisgaier, CL ;
Newton, RS ;
La Du, B .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (7-8) :892-904
[2]   Prolonged infusion of angiotensin II into normal rats induces stellate cell activation and proinflammatory events in liver [J].
Bataller, R ;
Gäbele, E ;
Schoonhoven, R ;
Morris, T ;
Lehnert, M ;
Yang, L ;
Brenner, DA ;
Rippe, RA .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2003, 285 (03) :G642-G651
[3]  
BOWCOCK AM, 1986, AM J HUM GENET, V39, P699
[4]   LINKAGE OF CYSTIC-FIBROSIS TO THE PRO-ALPHA-2(I) COLLAGEN GENE, COL1A2, ON CHROMOSOME-7 [J].
BUCHWALD, M ;
ZSIGA, M ;
MARKIEWICZ, D ;
PLAVSIC, N ;
KENNEDY, D ;
ZENGERLING, S ;
WILLARD, HF ;
TSIPOURAS, P ;
SCHMIEGELOW, K ;
SCHWARTZ, M ;
EIBERG, H ;
MOHR, J ;
BARKER, D ;
DONISKELLER, H ;
TSUI, LC .
CYTOGENETICS AND CELL GENETICS, 1986, 41 (04) :234-239
[5]   Inhibition of hepatic cell nuclear DNA fragmentation by zinc in carbon tetrachloride-treated rats [J].
Cabré, M ;
Ferré, N ;
Folch, J ;
Paternain, JL ;
Hernàndez, M ;
del Castillo, D ;
Joven, J ;
Camps, J .
JOURNAL OF HEPATOLOGY, 1999, 31 (02) :228-234
[6]   Paraoxonase-1 promoter haplotypes and serum paraoxonase: a predominant role for polymorphic position-107, implicating the Sp1 transcription factor [J].
Deakin, S ;
Leviev, I ;
Brulhart-Meynet, MC ;
James, RW .
BIOCHEMICAL JOURNAL, 2003, 372 (372) :643-649
[7]   Simvastatin modulates expression of the PON1 gene and increases serum paraoxonase -: A role for sterol regulatory element-binding protein-2 [J].
Deakin, S ;
Leviev, I ;
Guernier, S ;
James, RW .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2003, 23 (11) :2083-2089
[8]   Enzymatically active paraoxonase-1 is located at the external membrane of producing cells and released by a high affinity, saturable, desorption mechanism [J].
Deakin, S ;
Leviev, I ;
Gomaraschi, M ;
Calabresi, L ;
Franceschini, G ;
James, RW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (06) :4301-4308
[9]   Hepatocyte apoptosis and Fas expression are prominent features of human nonalcoholic steatohepatitis [J].
Feldstein, AE ;
Canbay, A ;
Angulo, P ;
Taniai, M ;
Burgart, LJ ;
Lindor, KD ;
Gores, GJ .
GASTROENTEROLOGY, 2003, 125 (02) :437-443
[10]   SREBP contributes to induction of collagen VI transcription by serum starvation [J].
Ferrari, A ;
Maretto, S ;
Girotto, D ;
Volpin, D ;
Bressan, GM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 313 (03) :600-605