TY - JOUR
T1 - Rapid effect of inhaled fluticasone propionate on airway responsiveness to adenosine 5 '-monophosphate in mild asthma
AU - Ketchell, R I
AU - Jensen, M W
AU - Lumley, P
AU - Wright, A M
AU - Allenby, M I
AU - O'Connor, B J
PY - 2002/10/1
Y1 - 2002/10/1
N2 - Inhaled adenosine 5'-monophosphate (AMP) has an "indirect" bronchoconstrictive effect through mast cell degranulation and mediator release, whereas inhaled histamine has a "direct" effect on smooth muscle. Prolonged treatment with inhaled glucocorticosteroids attenuates airway responsiveness (AR) to AMP and histamine. We investigated the early effects of inhaled fluticasone propionate (FP) therapy on AR in 3 consecutive double-blind, randomized, placebo-controlled crossover studies in steroid-naive subjects with mild asthma. In one study, each of 12 subjects received FP 1000 mug or matched placebo for 7 inhalations at. 12 hourly intervals; AR to AMP and FEV1 were measured 2 hours after the 3rd and 7th inhalations. In a second study, each of 12 subjects received FP 100, 250, or 1000 mug or matched placebo for 3 inhalations at 12 hourly intervals; AR to AMP and FEV1 were measured 2 hours after the 1st and 3rd inhalations. In a third study, each of 8 subjects received a single inhalation of FP 1000 mug or matched placebo; AR to histamine was measured 2 hours later. In the first study, FP 1000 mug significantly attenuated AR to AMP by 2.7 and 2.5 doubling doses after 3 and 7 inhalations, respectively (P less than or equal to .0001). In the second study, FP 100, 250, and 1000 mug significantly attenuated AR to AMP by 1.9, 2.2, and 2.7 doubling doses, respectively, after I inhalation and by 2.4, 2.2, and 3.2 doubling doses, respectively, after 3 inhalations (P :.0001); a small but significant increase in FEV1 (>0.15 L) was observed after 3 inhalations but not after I inhalation of FP irrespective of dose (P less than or equal to .05). In the third study, a single inhalation of FP 1000 mug had no effect on AR to histamine. We have demonstrated a reduction in AR to AMP but not AR to histamine within 2 hours of a single inhalation of FP. This reflects a rapid, topical anti-inflammatory action of inhaled FP by a mechanism of action that remains unknown.
AB - Inhaled adenosine 5'-monophosphate (AMP) has an "indirect" bronchoconstrictive effect through mast cell degranulation and mediator release, whereas inhaled histamine has a "direct" effect on smooth muscle. Prolonged treatment with inhaled glucocorticosteroids attenuates airway responsiveness (AR) to AMP and histamine. We investigated the early effects of inhaled fluticasone propionate (FP) therapy on AR in 3 consecutive double-blind, randomized, placebo-controlled crossover studies in steroid-naive subjects with mild asthma. In one study, each of 12 subjects received FP 1000 mug or matched placebo for 7 inhalations at. 12 hourly intervals; AR to AMP and FEV1 were measured 2 hours after the 3rd and 7th inhalations. In a second study, each of 12 subjects received FP 100, 250, or 1000 mug or matched placebo for 3 inhalations at 12 hourly intervals; AR to AMP and FEV1 were measured 2 hours after the 1st and 3rd inhalations. In a third study, each of 8 subjects received a single inhalation of FP 1000 mug or matched placebo; AR to histamine was measured 2 hours later. In the first study, FP 1000 mug significantly attenuated AR to AMP by 2.7 and 2.5 doubling doses after 3 and 7 inhalations, respectively (P less than or equal to .0001). In the second study, FP 100, 250, and 1000 mug significantly attenuated AR to AMP by 1.9, 2.2, and 2.7 doubling doses, respectively, after I inhalation and by 2.4, 2.2, and 3.2 doubling doses, respectively, after 3 inhalations (P :.0001); a small but significant increase in FEV1 (>0.15 L) was observed after 3 inhalations but not after I inhalation of FP irrespective of dose (P less than or equal to .05). In the third study, a single inhalation of FP 1000 mug had no effect on AR to histamine. We have demonstrated a reduction in AR to AMP but not AR to histamine within 2 hours of a single inhalation of FP. This reflects a rapid, topical anti-inflammatory action of inhaled FP by a mechanism of action that remains unknown.
UR - http://www.scopus.com/inward/record.url?scp=0036793972&partnerID=8YFLogxK
U2 - 10.1067/mai.2002.128486
DO - 10.1067/mai.2002.128486
M3 - Article
SN - 1097-6825
VL - 110
SP - 603
EP - 606
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 4
ER -