TY - JOUR
T1 - Topical salmeterol reduces protein content of nasal lavage fluid in response to allergen and histamine challenge
T2 - Double-blind cross-over placebo-controlled studies in adults
AU - Birchall, Martin A.
PY - 1996
Y1 - 1996
N2 - We have studied the effects of topical intranasal β-2-adrenoceptor agonists on nasal airflow resistance (R(naw)) and secretions. Pretreatment with salmeterol (SM) and salbutamol (SB) was given in two double-blind, placebo-controlled studies. In Protocol 1, 15 patients with allergic rhinitis were challenged with a threshold dose of allergen. R(naw) and lavage fluid total protein, albumin, mucin, lysozyme, tryptase, histamine, and eosinophil cationic protein (ECP) were measured. In Protocol 2, 20 normal subjects were challenged with ascending doses of histamine and R(naw) and lavage fluid total protein and albumin were measured. After allergen challenge, there was a significant, increase in R(naw), total protein, albumin, and tryptase. SM significantly attenuated the rise in total protein (post-allergen challenge mean 218 mcg/mL, 95% c.i. 16-447; SB 344, 45-641; placebo 365, 105-725: P = 0.036). SM significantly reduced albumin concentration at 30 minutes post-drug (post-histamine challenge geometric mean 17.1 mcg/mL, interquartile range 8.2-29.4; SB 25.1, 15.2-43.0; placebo 24.2, 16.6-37.8: P = 0.027). SM has acute effects on the nasal response to allergen in allergic rhinitis and to histamine in normal subjects. These results imply an effect on glands and blood vessels in vivo that may represent part of the drug's clinical activity.
AB - We have studied the effects of topical intranasal β-2-adrenoceptor agonists on nasal airflow resistance (R(naw)) and secretions. Pretreatment with salmeterol (SM) and salbutamol (SB) was given in two double-blind, placebo-controlled studies. In Protocol 1, 15 patients with allergic rhinitis were challenged with a threshold dose of allergen. R(naw) and lavage fluid total protein, albumin, mucin, lysozyme, tryptase, histamine, and eosinophil cationic protein (ECP) were measured. In Protocol 2, 20 normal subjects were challenged with ascending doses of histamine and R(naw) and lavage fluid total protein and albumin were measured. After allergen challenge, there was a significant, increase in R(naw), total protein, albumin, and tryptase. SM significantly attenuated the rise in total protein (post-allergen challenge mean 218 mcg/mL, 95% c.i. 16-447; SB 344, 45-641; placebo 365, 105-725: P = 0.036). SM significantly reduced albumin concentration at 30 minutes post-drug (post-histamine challenge geometric mean 17.1 mcg/mL, interquartile range 8.2-29.4; SB 25.1, 15.2-43.0; placebo 24.2, 16.6-37.8: P = 0.027). SM has acute effects on the nasal response to allergen in allergic rhinitis and to histamine in normal subjects. These results imply an effect on glands and blood vessels in vivo that may represent part of the drug's clinical activity.
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M3 - Article
AN - SCOPUS:0029794247
VL - 10
SP - 251
EP - 256
JO - American Journal of Rhinology and Allergy
JF - American Journal of Rhinology and Allergy
SN - 1945-8924
IS - 4
ER -