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1 Department of Animal Physiology, Lund University, S-223 62 Lund, Sweden; and 2 Cardiovascular Research Institute, University of California, San Francisco, California 94143-0130
The in
vivo effect of 48-h glucocorticoid and thyroid hormone
3,3',5-triiodine-L-thyronine (T3)
pretreatment on alveolar epithelial fluid transport was studied in
adult rats. An isosmolar 5% albumin solution was instilled, and
alveolar fluid clearance was studied for 1 h. Compared with controls,
dexamethasone pretreatment increased alveolar fluid clearance by 80%.
T3 pretreatment stimulated alveolar fluid clearance by
65%, and dexamethasone and T3 had additive effects
(132%). Propranolol did not inhibit alveolar fluid clearance in either
group, indicating that stimulation was not secondary to endogenous
-adrenergic stimulation. With the use of bromodeoxyuridine in vivo
labeling, there was no evidence of cell proliferation. Alveolar fluid
clearance was partially inhibited by amiloride in all groups.
Fractional amiloride inhibition was greater in dexamethasone- and
dexamethasone-plus-T3-pretreated rats than in control
animals, but less in T3-pretreated rats. In summary, pretreatment with dexamethasone, T3, or both in combination
upregulate in vivo alveolar fluid clearance similarly to
short-term
-adrenergic stimulation. The effects are mediated partly
by increased amiloride-sensitive Na+ transport, because the
stimulated alveolar fluid clearance was more amiloride sensitive than
in control rats. These observations may have clinical relevance because
glucocorticoid therapy is commonly used with acute lung injury.
acute lung injury; alveolar epithelium; amiloride;
-adrenergic
agonists; glucocorticoids; pulmonary edema; sodium transport
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