SUBSTANCE-P AND NEUROKININ-A IN HUMAN NASAL-MUCOSA

被引:149
作者
BARANIUK, JN
LUNDGREN, JD
OKAYAMA, M
GOFF, J
MULLOL, J
MERIDA, M
SHELHAMER, JH
KALINER, MA
机构
[1] NIAID, CLIN INVEST LAB, ALLERG DIS SECT, BETHESDA, MD 20892 USA
[2] NIH, CTR CLIN, DEPT MED, DIV CRIT CARE, BETHESDA, MD 20892 USA
[3] GEORGETOWN UNIV, DIV VIROL, WASHINGTON, DC 20057 USA
[4] GEORGETOWN UNIV HOSP, DEPT OTOLARYNGOL, WASHINGTON, DC 20007 USA
[5] GEORGETOWN UNIV HOSP, DEPT PEDIAT, WASHINGTON, DC 20007 USA
关键词
D O I
10.1165/ajrcmb/4.3.228
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The tachykinins substance P (SP) and neurokinin A (NKA) were studied in human inferior turbinate nasal mucosa by radioimmunoassay, immunohistochemistry, and autoradiography and for their effect upon mucus release in an in vitro culture system in order to infer their potential functions in the upper respiratory tract. Similar amounts of SP (1.03 +/- 0.12 pmol/g wet weight; mean +/- SEM; n = 26) and NKA (0.76 +/- 0.23; n = 7) were found. NKA and SP immunoreactive nerve fibers were found in the walls of arterioles, venules, and sinusoids and as individual fibers in gland acini, near the basement membrane, and in the epithelium. [I-125]SP bound to arterioles, venules, and glands. [I-125]NKA bound only to arterioles. In short-term explant culture of fragments of human nasal mucosa, both 1-mu-M SP and 1-mu-M NKA stimulated release of [H-3]glucosamine-labeled respiratory glycoconjugates. These results indicate that SP and NKA have similar distributions in nociceptive sensory nerves in human nasal mucosa. The distribution of [I-125]SP binding sites is consistent with a role for SP as a vasodilator and mucous secretagogue. The presence of [I-125] NKA binding sites on vessels suggests a primary role for NKA in regulating vasomotor tone.
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页码:228 / 236
页数:9
相关论文
共 46 条
[1]  
AURSUDKIJ B, 1988, J PHYSL, V398
[2]  
BARNES PJ, 1986, BR J PHARM, V89
[3]   INFLAMMATORY EDEMA INDUCED BY SYNERGISM BETWEEN CALCITONIN GENE-RELATED PEPTIDE (CGRP) AND MEDIATORS OF INCREASED VASCULAR-PERMEABILITY [J].
BRAIN, SD ;
WILLIAMS, TJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1985, 86 (04) :855-860
[4]   SUBSTANCE-P REGULATES THE VASODILATOR ACTIVITY OF CALCITONIN GENE-RELATED PEPTIDE [J].
BRAIN, SD ;
WILLIAMS, TJ .
NATURE, 1988, 335 (6185) :73-75
[5]   AUTORADIOGRAPHIC MAPPING OF SUBSTANCE-P RECEPTORS IN LUNG [J].
CASTAIRS, JR ;
BARNES, PJ .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1986, 127 (03) :295-296
[7]   FINE STRUCTURE OF BLOOD VESSELS OF HUMAN NASAL RESPIRATORY MUCOSA [J].
CAUNA, N ;
HINDERER, KH .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1969, 78 (04) :865-&
[8]   POTENT STIMULATION OF GLYCOPROTEIN-SECRETION IN CANINE TRACHEA BY SUBSTANCE-P [J].
COLES, SJ ;
NEILL, KH ;
REID, LM .
JOURNAL OF APPLIED PHYSIOLOGY, 1984, 57 (05) :1323-1327
[9]   MEASUREMENT OF CATECHOLAMINES, INDOLEAMINES, THYROTROPIN-RELEASING-HORMONE AND SUBSTANCE-P IN RAT AND HUMAN SPINAL-CORD USING A COMMON EXTRACTION METHOD [J].
COOPER, CL ;
MARSDEN, CA ;
BENNETT, GW .
JOURNAL OF NEUROSCIENCE METHODS, 1987, 22 (01) :31-39
[10]   COMPARISON OF NEUROKININ-A AND SUBSTANCE-P ON CARDIOVASCULAR AND AIRWAY FUNCTION IN MAN [J].
EVANS, TW ;
DIXON, CM ;
CLARKE, B ;
CONRADSON, TB ;
BARNES, PJ .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1988, 25 (02) :273-275