SULFIDOPEPTIDE LEUKOTRIENES IN ASTHMA

被引:63
作者
ARM, JP [1 ]
LEE, TH [1 ]
机构
[1] UMDS,GUYS HOSP,DEPT ALLERGY & ALLIED RESP DISORDERS,NATL ASTHMA CAMPAIGN,4TH FLOOR,HUNTS HOUSE,LONDON SE1 9RT,ENGLAND
关键词
ASTHMA; LEUKOTRIENES;
D O I
10.1042/cs0840501
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
No single mediator is responsible for the clinical and pathological events in bronchial asthma. Nevertheless, there is now substantial evidence that the sulphidopeptide leukotrienes play an important role in the pathophysiology of the disease. They are potent in eliciting bronchoconstriction, mucus production and vasodilatation, and may enhance the airways hyperresponsiveness that is characteristic of the disease. The sulphidopeptide leukotrienes are present in the airways of asthmatic patients and their release has been demonstrated in acute severe asthma. They are released during asthmatic attacks provoked by a range of stimuli. The evidence from studies using sulphidopeptide leukotriene antagonists and 5-LO inhibitors suggests strongly that sulphidopeptide leukotrienes contribute to the resting asthmatic airways tone and to the asthmatic responses elicited by exercise, allergen, aspirin and cold, dry air challenges. These mediators may also contribute to the airways hyperresponsiveness induced by allergen challenge of sensitized subjects. Preliminary results indicate that the administration of leukotriene receptor antagonists and 5-LO inhibitors may benefit patients with chronic asthma. Further studies are now needed to define better the role of these novel drugs in the management of the disease.
引用
收藏
页码:501 / 510
页数:10
相关论文
共 131 条
[31]   LEUKOTRIENES ARE POTENT CONSTRICTORS OF HUMAN BRONCHI [J].
DAHLEN, SE ;
HEDQVIST, P ;
HAMMARSTROM, S ;
SAMUELSSON, B .
NATURE, 1980, 288 (5790) :484-486
[32]   LEUKOTRIENES PROMOTE PLASMA LEAKAGE AND LEUKOCYTE ADHESION IN POST-CAPILLARY VENULES - INVIVO EFFECTS WITH RELEVANCE TO THE ACUTE INFLAMMATORY RESPONSE [J].
DAHLEN, SE ;
BJORK, J ;
HEDQVIST, P ;
ARFORS, KE ;
HAMMARSTROM, S ;
LINDGREN, JA ;
SAMUELSSON, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (06) :3887-3891
[33]  
DAVIDSON AB, 1987, AM REV RESPIR DIS, V135, P333
[34]   REQUIREMENT OF A 5-LIPOXYGENASE-ACTIVATING PROTEIN FOR LEUKOTRIENE SYNTHESIS [J].
DIXON, RAF ;
DIEHL, RE ;
OPAS, E ;
RANDS, E ;
VICKERS, PJ ;
EVANS, JF ;
GILLARD, JW ;
MILLER, DK .
NATURE, 1990, 343 (6255) :282-284
[35]   COMPARATIVE AIRWAY AND VASCULAR ACTIVITIES OF LEUKOTRIENE-C-1 AND LEUKOTRIENE-D INVIVO AND INVITRO [J].
DRAZEN, JM ;
AUSTEN, KF ;
LEWIS, RA ;
CLARK, DA ;
GOTO, G ;
MARFAT, A ;
COREY, EJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (07) :4354-4358
[36]   RECOVERY OF LEUKOTRIENE-E4 FROM THE URINE OF PATIENTS WITH AIRWAY-OBSTRUCTION [J].
DRAZEN, JM ;
OBRIEN, J ;
SPARROW, D ;
WEISS, ST ;
MARTINS, MA ;
ISRAEL, E ;
FANTA, CH .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 146 (01) :104-108
[37]  
DRAZEN JM, 1983, LEUKOTRIENES PROSTAC, P125
[38]   NOVEL TRANS-CELLULAR INTERACTION - CONVERSION OF GRANULOCYTE-DERIVED LEUKOTRIENE A4 TO CYSTEINYL-CONTAINING LEUKOTRIENES BY HUMAN-PLATELETS [J].
EDENIUS, C ;
HEIDVALL, K ;
LINDGREN, JA .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 178 (01) :81-86
[39]  
EVANS JM, 1988, BR J CLIN PHARM, V26, P667
[40]  
FEINMARK SJ, 1986, J BIOL CHEM, V261, P6466