共 12 条
Lung edema clearance:: 20 years of progress selected contribution:: Long-term effects of β2-adrenergic receptor stimulation on alveolar fluid clearance in mice
被引:34
|作者:
Sartori, C
Fang, X
McGraw, DW
Koch, P
Snider, ME
Folkesson, HG
Matthay, MA
机构:
[1] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[2] CHU Vaudois, Botnar Ctr Clin Res, CH-1011 Lausanne, Switzerland
[3] Univ Cincinnati, Dept Med, Cincinnati, OH 45267 USA
[4] Sepracor Marlborough, Marlborough, MA 01752 USA
[5] NE Ohio Univ, Coll Med, Dept Physiol, Rootstown, OH 44272 USA
关键词:
pulmonary edema;
acute lung injury;
lung fluid balance;
alveolar epithelium;
D O I:
10.1152/japplphysiol.00275.2002
中图分类号:
Q4 [生理学];
学科分类号:
071003 ;
摘要:
Stimulation of active fluid transport with beta-adrenergic receptor (betaAR) agonists can accelerate the resolution of alveolar edema. However, chronic betaAR-agonist administration may cause betaAR desensitization and downregulation that may impair physiological responsiveness to betaAR-agonist stimulation. Therefore, we measured baseline and terbutaline- (10(-3) M) stimulated alveolar fluid clearance in mice that received subcutaneously (miniosmotic pumps) either saline or albuterol (2 mg.kg(-1).day(-1)) for 1, 3, or 6 days. Continuous albuterol administration increased plasma albuterol levels (10(-5) M), an effect that was associated with 1) a significant decrease in betaAR density and 2) attenuation, but not ablation, of maximal terbutaline- induced cAMP production. Forskolin-mediated cAMP-release was unaffected. Continuous albuterol infusion stimulated alveolar fluid clearance on day 1 but did not increase alveolar fluid clearance on days 3 and 6. However, terbutaline- stimulated alveolar fluid clearance in albuterol-treated mice was not reduced compared with saline-treated mice. Despite significant reductions in betaAR density and agonist-mediated cAMP production by long-term betaAR-agonist exposure, maximal betaAR-agonist-mediated increase in alveolar fluid clearance is not diminished in mice.
引用
收藏
页码:1875 / 1880
页数:6
相关论文