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Am J Physiol Lung Cell Mol Physiol 290: L649-L660, 2006. First published October 28, 2005; doi:10.1152/ajplung.00205.2005
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EDITORIAL FOCUS

RNA interference for {alpha}-ENaC inhibits rat lung fluid absorption in vivo

Tianbo Li and Hans G. Folkesson

Department of Physiology and Pharmacology, Northeastern Ohio Universities College of Medicine, Rootstown, Ohio

Submitted 4 May 2005 ; accepted in final form 20 October 2005

We used siRNA against the {alpha}-ENaC (epithelial Na channel) subunit to investigate ENaC involvement in lung fluid absorption in rats by the impermeable tracer technique during baseline and after beta-adrenoceptor stimulation by terbutaline. Terbutaline stimulation of lung fluid absorption increased fluid absorption by 165% in pSi-0-pretreated rat lungs (irrelevant siRNA-generating plasmid). Terbutaline failed to increase lung fluid absorption in rats given the specific {alpha}-ENaC siRNA-generating plasmid (pSi-4). pSi-4 pretreatment reduced baseline lung fluid absorption by ~30%. {alpha}-ENaC was undetectable in pSi-4-pretreated lungs, regardless of condition but was normal in pSi-0-pretreated lungs. We carried out a dose-response analysis where rats were given 0–200 µg/kg body wt pSi-4, and {alpha}-ENaC mRNA and protein expressions were analyzed. To reach IC50 for {alpha}-ENaC mRNA expression, 32 µg/kg body wt pSi-4 was needed, and to reach IC50 for {alpha}-ENaC protein expression, 59 µg/kg body wt pSi-4 was needed. We tested for lung tissue specificity and found no changes in beta-ENaC expression, at either mRNA or protein level, as well as no changes in {alpha}1-Na-K-ATPase protein expression. We isolated alveolar epithelial type II cells 24 h after in vivo pSi-4 pretreatment. In these cells, {alpha}-ENaC mRNA was undetectable, demonstrating that alveolar epithelial ENaC expression was attenuated after intratracheal {alpha}-ENaC siRNA-generating plasmid DNA instillation. We tested for organ specificity and found no changes in kidney {alpha}- and beta-ENaC mRNA and protein expression. Thus we provide conclusive evidence that beta-adrenoceptor stimulation of lung fluid absorption is critically ENaC dependent, whereas baseline lung fluid absorption seemed less ENaC dependent.

alveolar fluid clearance; amiloride sensitivity; beta-adrenoceptor; sodium transport; small interfering RNA; epithelial sodium channel



Address for reprint requests and other correspondence: H. G. Folkesson, Dept. of Physiology and Pharmacology, Northeastern Ohio Universities College of Medicine, 4209 State Route 44, PO Box 95, Rootstown, OH 44272-0095 (e-mail: hgfolkes{at}neoucom.edu)




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