Oxidative stress in severe pulmonary hypertension

被引:283
作者
Bowers, R
Cool, C
Murphy, RC
Tuder, RM
Hopken, MW
Flores, SC
Voelkel, NF
机构
[1] Univ Colorado, Hlth Sci Ctr, Pulm Hypertens Ctr, Div Pulm Sci & Crit Care Med,Natl Jewish Med & Re, Denver, CO 80262 USA
[2] Johns Hopkins Univ, Dept Pathol, Cardiopulm Sect, Baltimore, MD 21205 USA
关键词
nitrotyrosine; superoxide dismutase; 5-oxo-eicosatetraenoic acid; pulmonary hypertension;
D O I
10.1164/rccm.200301-147OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Severe pulmonary hypertension (PH) occurs in a primary or "unexplained" form and in a group of secondary forms associated with a number of diseases. Because the lung tissue from patients with severe PH demonstrates complex vascular lesions, which contain inflammatory cells, we wondered whether the lung tissue from patients with severe PH was "under oxidative stress." We used immunohistochemistry to localize nitrotyrosine and 8-hydroxy guanosine in the lung tissue sections from patients with primary and secondary PH. In some lung tissue extracts, the eicosanoid metabolites 5-oxo-eicosatetraenoic acid, leukotriene B-4 5-hydroxyeicosatetraenoic acid (HETE), 12-HETE, and 15-HETE were measured using mass spectroscopy, and superoxide dismutase amount and activity were measured. Nitrotyrosine expression was ubiquitous in all PH lungs, and 5-oxo-eicosatetraenoic acid and HETE levels were elevated in the lungs of patients with severe PH but not in those lungs that were from the patients with severe PH treated chronically with prostacyclin. We conclude that indeed the lungs from patients with severe PH are under oxidative stress and that chronic prostacyclin infusion has an antiinflammatory effect on the lung tissue.
引用
收藏
页码:764 / 769
页数:6
相关论文
共 40 条
[1]   Endothelial NADPH oxidase as the source of oxidants in lungs exposed to ischemia or high K+ [J].
Al-Mehdi, AB ;
Zhao, GC ;
Dodia, C ;
Tozawa, K ;
Costa, K ;
Muzykantov, V ;
Ross, C ;
Blecha, F ;
Dinauer, M ;
Fisher, AB .
CIRCULATION RESEARCH, 1998, 83 (07) :730-737
[2]  
ANREADIS AA, 2003, FREE RADIC BIOL MED, V35, P213
[3]   Nitric oxide deficiency in fenfluramine- and dexfenfluramine-induced pulmonary hypertension [J].
Archer, SL ;
Djaballah, K ;
Humbert, M ;
Weir, EK ;
Fartoukh, M ;
DalL'Ava-Santucci, J ;
Mercier, JC ;
Simonneau, G ;
Dinh-Xuan, AT .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 158 (04) :1061-1067
[4]   Physiological functions of thioredoxin and thioredoxin reductase [J].
Arnér, ESJ ;
Holmgren, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (20) :6102-6109
[5]  
Baldus S, 2001, J CLIN INVEST, V108, P1759
[6]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[7]   PATHOLOGICAL IMPLICATIONS OF NITRIC-OXIDE, SUPEROXIDE AND PEROXYNITRITE FORMATION [J].
BECKMAN, JS ;
CROW, JP .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1993, 21 (02) :330-334
[8]   A novel glutathione containing eicosanoid (FOG7) chemotactic for human granulocytes [J].
Bowers, RC ;
Hevko, J ;
Henson, PM ;
Murphy, RC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (39) :29931-29934
[9]   Role of oxidants in NF-κB activation and TNF-α gene transcription induced by hypoxia and endotoxin [J].
Chandel, NS ;
Trzyna, WC ;
McClintock, DS ;
Schumacker, PT .
JOURNAL OF IMMUNOLOGY, 2000, 165 (02) :1013-1021
[10]   The arachidonate 12/15 lipoxygenases -: A review of tissue expression and biologic function [J].
Conrad, DJ .
CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, 1999, 17 (1-2) :71-89