Hemodynamic and biochemical effects of 100% oxygen breathing in humans

被引:51
作者
Milone, SD
Newton, GE
Parker, JD
机构
[1] Univ Toronto, Dept Pharmacol, Toronto, ON, Canada
[2] Mt Sinai Hosp, Dept Med, Div Cardiol, Toronto, ON M5G 1X5, Canada
关键词
oxygen; nitroglycerin; free radicals; blood pressure; heart rate; plethysmography;
D O I
10.1139/cjpp-77-2-124
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
High concentrations of inspired oxygen have been reported to have significant hemodynamic effects that may be related to increased free radical production. If oxygen therapy increases free radical production, it may also modify hemodynamic responses to a nitric oxide donor. Twenty-nine healthy male volunteers were studied using randomized, double-blind, placebo-controlled, crossover designs to determine whether oxygen therapy is associated with hemodynamic and forearm vascular effects. We measured hemodynamic parameters and forearm vascular responses before and 1 h after exposure to 100% oxygen versus medical air. Plasma 8-iso-PGF(2 alpha) and plasma vitamin C were measured to assess the biochemical effects of oxygen administration. Hemodynamic measurements were also made following the acute administration of sublingual nitroglycerin. Oxygen therapy caused no significant change in blood pressure, plasma 8-iso-PGF(2 alpha), or vitamin C. Oxygen did cause a significant reduction in heart rate and forearm blood flow, and an increase in peripheral vascular resistance. Oxygen caused no change in the hemodynamic response to nitroglycerin. Therefore, in healthy young adults, therapy with 100% oxygen does not affect blood pressure, despite causing an increase in vascular resistance, is not associated with evidence of increased free radical injury, and does not affect the hemodynamic responses to nitroglycerin.
引用
收藏
页码:124 / 130
页数:7
相关论文
共 50 条
  • [31] FORMATION OF F-2-ISOPROSTANES DURING OXIDATION OF HUMAN LOW-DENSITY-LIPOPROTEIN AND PLASMA BY PEROXYNITRITE
    MOORE, KP
    DARLEYUSMAR, V
    MORROW, J
    ROBERTS, LJ
    [J]. CIRCULATION RESEARCH, 1995, 77 (02) : 335 - 341
  • [32] INCREASE IN CIRCULATING PRODUCTS OF LIPID-PEROXIDATION (F-2-ISOPROSTANES) IN SMOKERS - SMOKING AS A CAUSE OF OXIDATIVE DAMAGE
    MORROW, JD
    FREI, B
    LONGMIRE, AW
    GAZIANO, JM
    LYNCH, SM
    SHYR, Y
    STRAUSS, WE
    OATES, JA
    ROBERTS, LJ
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (18) : 1198 - 1203
  • [33] FORMATION OF NOVEL NON-CYCLOOXYGENASE-DERIVED PROSTANOIDS (F2-ISOPROSTANES) IN CARBON-TETRACHLORIDE HEPATOTOXICITY - AN ANIMAL-MODEL OF LIPID-PEROXIDATION
    MORROW, JD
    AWAD, JA
    KATO, T
    TAKAHASHI, K
    BADR, KF
    ROBERTS, LJ
    BURK, RF
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (06) : 2502 - 2507
  • [34] MOTCHNIK PA, 1994, METHOD ENZYMOL, V234, P269
  • [35] EVIDENCE FOR ENHANCED VASCULAR SUPEROXIDE ANION PRODUCTION IN NITRATE TOLERANCE - A NOVEL MECHANISM UNDERLYING TOLERANCE AND CROSS-TOLERANCE
    MUNZEL, T
    SAYEGH, H
    FREEMAN, BA
    TARPEY, MM
    HARRISON, DG
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (01) : 187 - 194
  • [36] Narkiewicz K, 1998, CIRCULATION, V97, P943
  • [37] HYPERBARIC-OXYGEN THERAPY INCREASES FREE-RADICAL LEVELS IN THE BLOOD OF HUMANS
    NARKOWICZ, CK
    VIAL, JH
    MCCARTNEY, PW
    [J]. FREE RADICAL RESEARCH COMMUNICATIONS, 1993, 19 (02): : 71 - 80
  • [38] PACEASCIAK CR, 1987, CLIN INVEST MED, V10, P117
  • [39] PELLETIER O, 1970, AM J CLIN NUTR, V23, P520
  • [40] Modulation of oxidant stress in vivo in chronic cigarette smokers
    Reilly, M
    Delanty, N
    Lawson, JA
    FitzGerald, GA
    [J]. CIRCULATION, 1996, 94 (01) : 19 - 25