LIPID-PEROXIDATION ABNORMALITIES IN HEMODIALYZED PATIENTS

被引:127
|
作者
PAUL, JL
SALL, ND
SONI, T
POIGNET, JL
LINDENBAUM, A
MAN, NK
MOATTI, N
RAICHVARG, D
机构
[1] FAC SCI PHARMACEUT & BIOL CHATENAY MALABRY,BIOCHIM LAB,CHATENAY MALABRY,FRANCE
[2] UNIV CHEIKH ANTA DIOP,BIOCHIM MED LAB,DAKAR,SENEGAMBIA
[3] HOP BECLERE,BIOCHIM LAB,CLAMART,FRANCE
[4] HOP NECKER ENFANTS MALAD,DEPT NEPHROL,INSERM,U90,F-75730 PARIS 15,FRANCE
[5] HOP COCHIN,BIOCHIM LAB,F-75674 PARIS 14,FRANCE
[6] CTR MED E RIST,PARIS,FRANCE
来源
NEPHRON | 1993年 / 64卷 / 01期
关键词
LIPID PEROXIDATION; GLUTATHIONE PEROXIDASE; SUPEROXIDE DISMUTASE; HEMODIALYSIS;
D O I
10.1159/000187287
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
In order to test the existence of a possible oxidative damage during hemodialysis, plasma conjugated dienes (CD), plasma and red blood cell (RBC) thiobarbituric acid (TBA) reactants were investigated in 25 patients receiving regular dialysis treatment (RDT). The RBC TBA reactant concentration was significantly increased in RDT patients in comparison with healthy subjects. The extracellular antioxidant systems were evaluated by the assay of plasma antioxidant activity, plasma tocopherol, urate, transferrin, haptoglobin and ceruloplasmin levels. Except urate and transferrin, none of these parameters were different between the two groups. On the other hand, in RDT patients, RBC superoxide dismutase (SOD) and glutathione peroxidase (GPX) activities were significantly lower than in healthy subjects. There was an inverse correlation between decreased RBC GPX and RBC TBA reactant concentration. These results show in RDT patients the existence of an oxidizing stress, mainly intracellular, which could be due, in part, to a decrease in SOD and GPX activities.
引用
收藏
页码:106 / 109
页数:4
相关论文
共 50 条
  • [21] LIPID-PEROXIDATION IN THE BLOOD OF PATIENTS WITH PRIMARY GLAUCOMA
    BIRICH, TV
    BIRISH, TA
    MARCHENKO, LN
    REMIZONOVA, DB
    FEDULOV, AS
    VESTNIK OFTALMOLOGII, 1986, (01) : 13 - 15
  • [22] LIPID-PEROXIDATION AND ANTIOXIDANT STATUS IN BURN PATIENTS
    GEE, DL
    LITOV, RE
    CLINICAL RESEARCH, 1991, 39 (02): : A658 - A658
  • [23] LIPID-PEROXIDATION IN HOMOCYSTEINAEMIA
    BLOM, HJ
    ENGELEN, DPE
    BOERS, GHJ
    STADHOUDERS, AM
    SENGERS, RCA
    DEABREU, R
    TEPOELEPOTHOFF, MTWB
    TRIJBELS, JMF
    JOURNAL OF INHERITED METABOLIC DISEASE, 1992, 15 (03) : 419 - 422
  • [24] LIPID-PEROXIDATION IN SALMONELLOSIS
    OKONENKO, LB
    LABORATORNOE DELO, 1987, (01): : 55 - 58
  • [25] ROLES OF LIPID-PEROXIDATION
    DIPLOCK
    HIGGS
    PRYOR
    INGOLD
    FINER
    SLATER
    MCMURRAY
    WILLSON
    PACKER
    JACKSON
    CIBA FOUNDATION SYMPOSIA, 1983, 101 : 241 - 246
  • [26] LIPID-PEROXIDATION AND CANCER
    DIANZANI, MU
    CRITICAL REVIEWS IN ONCOLOGY/HEMATOLOGY, 1993, 15 (02) : 125 - 147
  • [27] LIPID-PEROXIDATION IN PATIENTS WITH ESSENTIAL-HYPERTENSION
    UYSAL, M
    BULUR, H
    SENER, D
    OZ, H
    INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS, 1986, 24 (09) : 474 - 476
  • [28] LIPID-PEROXIDATION IN ERYTHROCYTES
    CLEMENS, MR
    WALLER, HD
    CHEMISTRY AND PHYSICS OF LIPIDS, 1987, 45 (2-4) : 251 - 268
  • [29] CHEMISTRY OF LIPID-PEROXIDATION
    PORTER, NA
    METHODS IN ENZYMOLOGY, 1984, 105 : 273 - 282
  • [30] METALS AND LIPID-PEROXIDATION
    SUNDERMAN, FW
    ACTA PHARMACOLOGICA ET TOXICOLOGICA, 1986, 59 : 248 - 255