Abstract | BACKGROUND: METHODS: RESULTS:
Formoterol had a minor effect, whereas budesonide concentration-dependently decreased CF transport by MRP1. Remarkably, addition of formoterol to the highest concentration of budesonide increased CF transport. Ipratropium bromide inhibited CF transport at low concentrations and tended to increase CF transport at higher levels. NAC increased CF transport by MRP1 in a concentration-dependent manner. CONCLUSIONS: Our data suggest that, besides their positive effects on respiratory symptoms, budesonide, formoterol, ipratropium bromide, and NAC modulate MRP1 activity in bronchial epithelial cells. Further studies are required to assess whether stimulation of MRP1 activity is beneficial for long-term treatment of COPD.
|
Authors | Margaretha van der Deen, Sandra Homan, Hetty Timmer-Bosscha, Rik J Scheper, Wim Timens, Dirkje S Postma, Elisabeth G de Vries |
Journal | International journal of chronic obstructive pulmonary disease
(Int J Chron Obstruct Pulmon Dis)
Vol. 3
Issue 3
Pg. 469-75
( 2008)
ISSN: 1176-9106 [Print] New Zealand |
PMID | 18990976
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Bronchodilator Agents
- Cholinergic Antagonists
- Ethanolamines
- Expectorants
- Multidrug Resistance-Associated Proteins
- Budesonide
- Ipratropium
- Formoterol Fumarate
- Acetylcysteine
- multidrug resistance-associated protein 1
|
Topics |
- Acetylcysteine
(metabolism, therapeutic use)
- Biological Transport
(drug effects)
- Bronchi
(cytology)
- Bronchodilator Agents
(metabolism, therapeutic use)
- Budesonide
(metabolism, therapeutic use)
- Cholinergic Antagonists
(metabolism, therapeutic use)
- Drug Resistance, Multiple
(physiology)
- Epithelial Cells
(drug effects, physiology)
- Ethanolamines
(metabolism, therapeutic use)
- Expectorants
(metabolism, therapeutic use)
- Flow Cytometry
- Formoterol Fumarate
- Humans
- In Vitro Techniques
- Ipratropium
(metabolism, therapeutic use)
- Multidrug Resistance-Associated Proteins
(drug effects, physiology)
- Oxidative Stress
(drug effects, physiology)
- Pulmonary Disease, Chronic Obstructive
(drug therapy, metabolism)
|