Effect of propofol on oxidative stress in an in vitro model of anoxia-reoxygenation in the rat brain

被引:43
作者
De La Cruz, JP [1 ]
Villalobos, MA
Sedeño, G
De La Cuesta, FS
机构
[1] Univ Malaga, Sch Med, Dept Therapeut, E-29071 Malaga, Spain
[2] Univ Malaga, Sch Med, Dept Pharmacol, E-29071 Malaga, Spain
[3] Univ Malaga, Sch Med, Dept Human Anat, E-29071 Malaga, Spain
关键词
propofol; ischemia; reperfusion; oxidative stress; glutathione; lipid peroxidation;
D O I
10.1016/S0006-8993(98)00516-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Propofol, an intravenous anaesthetic, is similar in chemical structure to the active nucleus of antioxidant substances such as alpha-tocopherol (vitamin E), The present study was designed to lest whether propofol had antioxidant effects in an in vitro model of anoxia-reoxygenation in slices of rat brain. We used seven experimental groups: (1) control oxygenated tissue (2) tissue subjected to anoxia for 20 min and reoxygenation for 3 h; and tissues processed as described and incubated with (3) Intralipid (commercial solvent for propofol), or propofol at a concentration of (4) 10 mu mol/l, (5) 50 mu mol/l, (6) 150 mu mol/l or (7) 300 mu mol/l. The production of lipid peroxides was quantified as thiobarbituric acid reactive substances (TBARS); tissular glutathione production and the activities of glutathione peroxidase (GSHpx), glutathione reductase (GSSGrd) and glutathione transferase (GSHtf) were also measured. Reoxygenation led to tissular oxidative stress, which was curtailed by propofol. The anaesthetic led to a 47% reduction in TBARS, a 165% increased in the reperfusion-inhibiting glutathione content, a 47% decrease in GSHpx activity, and an 87% increase in GSHtf activity. Intralipid had no effect on any of the parameters studied here. We conclude that propofol has a clear antioxidant effect in rat brain tissue subjected to anoxia-reoxygenation. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:136 / 144
页数:9
相关论文
共 32 条
  • [1] THE WIDELY USED ANESTHETIC AGENT PROPOFOL CAN REPLACE ALPHA-TOCOPHEROL AS AN ANTIOXIDANT
    AARTS, L
    VANDERHEE, R
    DEKKER, I
    DEJONG, J
    LANGEMEIJER, H
    BAST, A
    [J]. FEBS LETTERS, 1995, 357 (01) : 83 - 85
  • [2] ARAI H, 1987, J CLIN BIOCHEM NUTR, V3, P227
  • [3] POSTTREATMENT WITH EPC-K1, AN INHIBITOR OF LIPID-PEROXIDATION AND OF PHOSPHOLIPASE-A2 ACTIVITY, REDUCES FUNCTIONAL DEFICITS AFTER GLOBAL-ISCHEMIA IN RATS
    BLOCK, F
    KUNKEL, M
    SONTAG, KH
    [J]. BRAIN RESEARCH BULLETIN, 1995, 36 (03) : 257 - 260
  • [4] BOSSMAN HB, 1969, STRUCTURE FUNCTION N, V3, P1
  • [5] BRAIN INJURY, EDEMA, AND VASCULAR-PERMEABILITY CHANGES INDUCED BY OXYGEN-DERIVED FREE-RADICALS
    CHAN, PH
    SCHMIDLEY, JW
    FISHMAN, RA
    LONGAR, SM
    [J]. NEUROLOGY, 1984, 34 (03) : 315 - 320
  • [6] COCKSHOTT ID, 1985, POSTGRAD MED J, V61, P45
  • [7] DAVIS RJ, 1987, FASEB J, V46, P799
  • [8] De Alba J., 1997, Methods and Findings in Experimental and Clinical Pharmacology, V19, P116
  • [9] INHIBITION OF FERROUS-INDUCED LIPID-PEROXIDATION BY PYRIMIDO-PYRIMIDINE DERIVATIVES IN HUMAN LIVER MEMBRANES
    DELACRUZ, JP
    CARRASCO, T
    ORTEGA, G
    DELACUESTA, FS
    [J]. LIPIDS, 1992, 27 (03) : 192 - 194
  • [10] Propofol inhibits in vitro platelet aggregation in human whole blood
    DeLaCruz, JP
    Carmona, JA
    Paez, MV
    Blanco, E
    DeLaCuesta, FS
    [J]. ANESTHESIA AND ANALGESIA, 1997, 84 (04) : 919 - 921