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EDITORIAL FOCUS
-ENaC inhibits rat lung fluid absorption in vivo
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
-ENaC (epithelial Na channel) subunit to investigate ENaC involvement in lung fluid absorption in rats by the impermeable tracer technique during baseline and after
-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
-ENaC siRNA-generating plasmid (pSi-4). pSi-4 pretreatment reduced baseline lung fluid absorption by
30%.
-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 0200 µg/kg body wt pSi-4, and
-ENaC mRNA and protein expressions were analyzed. To reach IC50 for
-ENaC mRNA expression, 32 µg/kg body wt pSi-4 was needed, and to reach IC50 for
-ENaC protein expression, 59 µg/kg body wt pSi-4 was needed. We tested for lung tissue specificity and found no changes in
-ENaC expression, at either mRNA or protein level, as well as no changes in
1-Na-K-ATPase protein expression. We isolated alveolar epithelial type II cells 24 h after in vivo pSi-4 pretreatment. In these cells,
-ENaC mRNA was undetectable, demonstrating that alveolar epithelial ENaC expression was attenuated after intratracheal
-ENaC siRNA-generating plasmid DNA instillation. We tested for organ specificity and found no changes in kidney
- and
-ENaC mRNA and protein expression. Thus we provide conclusive evidence that
-adrenoceptor stimulation of lung fluid absorption is critically ENaC dependent, whereas baseline lung fluid absorption seemed less ENaC dependent.
alveolar fluid clearance; amiloride sensitivity;
-adrenoceptor; sodium transport; small interfering RNA; epithelial sodium channel
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