BLOCKADE OF EOSINOPHIL MIGRATION BY 5-LIPOXYGENASE AND CYCLOOXYGENASE INHIBITION IN EXPLANTED GUINEA-PIG TRACHEALIS

被引:11
作者
MUNOZ, NM
LEFF, AR
机构
[1] UNIV CHICAGO, DEPT MED, PULM & CRIT CARE MED SECT, CHICAGO, IL 60637 USA
[2] UNIV CHICAGO, DEPT PHARMACOL & PHYSIOL SCI, CHICAGO, IL 60637 USA
[3] UNIV CHICAGO, DIV BIOL SCI, COMM CLIN PHARMACOL, CHICAGO, IL 60637 USA
[4] UNIV CHICAGO, DIV BIOL SCI, COMM CELL PHYSIOL, CHICAGO, IL 60637 USA
关键词
AIRWAY CONTRACTION; CHEMOTAXIS; CYCLOOXYGENASE;
D O I
10.1152/ajplung.1995.268.3.L446
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We studied the effects of 5-lipoxygenase inhibition with A63162 and cyclooxygenase inhibition with indomethacin (INDO) on 1) eosinophil chemotaxis and 2) airway narrowing caused by 10(-6) M formyl-Met-Leu-Phe (fMLP) in tracheal explants from guinea pigs. Airway narrowing was assessed by calibrated micrometry, and eosinophil migration from the lamina propria was expressed as number of eosinophils contained per 1 cm tracheal segment. After 120 min, treatment with fMLP caused an increase in luminal eosinophils from 6,804 +/- 1,786 to 303,347 +/- 75,609 cells (P < 0.001); airway diameter narrowed by 20.4 +/- 1.4%. In six preparations, A63162 inhibited airway narrowing caused by fMLP by 54.9 +/- 6.1%; INDO had a similar effect on airway diameter. However, maximal inhibition of eosinophil migration was greater after 10(-6) M A63162 (38,393 +/- 7,434 cells; P < 0.001 vs. fMLP alone) than after treatment with 10(-5) M INDO (123,547 +/- 19,499 cells; P < 0.05). We demonstrate a method that permits simultaneous measurements of eosinophil migration and airway smooth muscle contraction in a guinea pig tracheal explant preparation. Our data suggest that eosinophil chemotaxis and changes in internal airway diameter are caused by activation of both 5-lipoxygenase and cyclooxygenase pathways and that cell migration is independent of the physical consequences of airway smooth muscle contraction.
引用
收藏
页码:L446 / L454
页数:9
相关论文
共 19 条
[2]   LTB4, A POTENT CHEMOTACTIC FACTOR FOR PURIFIED GUINEA-PIG EOSINOPHILS - INTERFERENCE OF PAF-ACETHER ANTAGONISTS [J].
COEFFIER, E ;
JOSEPH, D ;
VARGAFTIG, BB .
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1991, 13 (2-3) :273-280
[3]   DEVELOPMENT OF A PROLONGED EOSINOPHIL-RICH INFLAMMATORY LEUKOCYTE INFILTRATION IN THE GUINEA-PIG ASTHMATIC RESPONSE TO OVALBUMIN INHALATION [J].
DUNN, CJ ;
ELLIOTT, GA ;
OOSTVEEN, JA ;
RICHARDS, IM .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1988, 137 (03) :541-547
[4]   ONLY THE CHEMOTACTIC SUB-POPULATION OF HUMAN-BLOOD MONOCYTES EXPRESSES RECEPTORS FOR THE CHEMOTACTIC PEPTIDE N-FORMYLMETHIONYL-LEUCYL-PHENYLALANINE [J].
FALK, W ;
HARVATH, L ;
LEONARD, EJ .
INFECTION AND IMMUNITY, 1982, 36 (02) :450-454
[5]   THE EOSINOPHIL AND THE PATHOPHYSIOLOGY OF ASTHMA [J].
FRIGAS, E ;
GLEICH, GJ .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1986, 77 (04) :527-537
[6]  
GALLIN JI, 1988, METHOD ENZYMOL, V162, P59
[7]  
HENOCQ E, 1986, LANCET, V1, P1378
[8]  
Luna L.G., 1968, MANUAL HISTOLOGIC ST, P111
[9]  
Luna LG, 1992, HISTOPATHOLOGIC METH, P255
[10]   EFFECT OF AIRWAY INFLAMMATION ON SMOOTH-MUSCLE SHORTENING AND CONTRACTILITY IN GUINEA-PIG TRACHEALIS [J].
MITCHELL, RW ;
NDUKWU, IM ;
ARBETTER, K ;
SOLWAY, J ;
LEFF, AR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (06) :L549-L554