Functional roles of nasal nitric oxide in nasal patency and mucociliary function

被引:12
作者
Imada, M
Nonaka, S
Kobayashi, Y
Iwamoto, J
机构
[1] Asahikawa Med Coll, Dept Otorhinolaryngol, Asahikawa, Hokkaido 0788302, Japan
[2] Asahikawa Med Coll, Div Appl Physiol, Asahikawa, Hokkaido 078, Japan
关键词
flutropium bromide; saccharin time; sodium nitroprusside;
D O I
10.1080/00016480260092327
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
The purpose of this study was twofold: (i) to clarify whether it is possible to change the amount of nasal nitric oxide (NO) artificially; and (ii) to confirm that the artificially altered nasal NO has biological properties such as vasodilatation and mucociliary function. We measured nasal NO and nasal airway resistance (NAR) in healthy subjects before and after topical administration of sodium nitroprusside (SNP), an NO donor. We also measured nasal NO and saccharin transport time after administration of SNP or L-N-G-nitroarginine methylester (L-NAME), a NO synthase inhibitor. In addition, we examined the effect of SNP and L-NAME on nasal NO and saccharin transport time after pretreatment with flutropium bromide (FB), an anticholinergic agent. Administration of SNP elicited increases in nasal NO and NAR in a dose-dependent manner. Nasal NO decreased significantly after topical administration of L-NAME. Saccharin transport time, an indicator of mucociliary function, was shortened after topical administration of SNP and prolonged after administration of L-NAME. Moreover, these phenomena were observed even after pretreatment with F B. These results suggest that artificially altered nasal NO may affect NAR and mucociliary function.
引用
收藏
页码:513 / 519
页数:7
相关论文
共 23 条
[1]  
ALVING K, 1993, EUR RESPIR J, V6, P1368
[2]  
Clement P A, 1984, Rhinology, V22, P151
[3]   Expression of nitric oxide synthase human nasal mucosa [J].
Furukawa, K ;
Harrison, DG ;
Saleh, D ;
Shennib, H ;
Chagnon, FP ;
Giaid, A .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (02) :847-850
[4]   TOPICAL NITROPRUSSIDE MAY REDUCE HISTAMINE-INDUCED PLASMA EXUDATION IN HUMAN NASAL AIRWAYS [J].
GREIFF, L ;
ANDERSSON, M ;
SVENSSON, C ;
NILSSON, M ;
ERJEFALT, I ;
ERJEFALT, JS ;
PERSSON, CGA .
ALLERGY, 1995, 50 (07) :593-597
[5]   DISTRIBUTION OF NADPH-DIAPHORASE POSITIVE NERVE-FIBERS IN THE RAT NASAL-MUCOSA [J].
HANAZAWA, T ;
MOTOSUGI, H ;
KONNO, A ;
KANEKO, T ;
TANAKA, K ;
CHIBA, T .
NEUROSCIENCE LETTERS, 1993, 159 (1-2) :71-74
[6]   Distribution and origin of nitric oxide synthase-containing nerve fibers in human nasal mucosa [J].
Hanazawa, T ;
Tanaka, K ;
Chiba, T ;
Konno, A .
ACTA OTO-LARYNGOLOGICA, 1997, 117 (05) :735-737
[7]   Measurement of nitric oxide in human nasal airway [J].
Imada, M ;
Iwamoto, J ;
Nonaka, S ;
Kobayashi, Y ;
Unno, T .
EUROPEAN RESPIRATORY JOURNAL, 1996, 9 (03) :556-559
[8]  
IWAMOTO J, 1998, NAG S SPORTS SCI, P21
[9]   MODULATION OF AIRWAY EPITHELIAL-CELL CILIARY BEAT FREQUENCY BY NITRIC-OXIDE [J].
JAIN, B ;
RUBINSTEIN, I ;
ROBBINS, RA ;
LEISE, KL ;
SISSON, JH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 191 (01) :83-88
[10]   Nitric oxide (NO) production in the upper airways is decreased in chronic sinusitis [J].
Lindberg, S ;
Cervin, A ;
Runer, T .
ACTA OTO-LARYNGOLOGICA, 1997, 117 (01) :113-117