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NF‐κB involvement in the induction of high affinity CAT‐2 in lipopolysaccharide‐stimulated rat lungs
Author(s) -
Huang C.J.,
Tsai P.S.,
Lu Y.T.,
Cheng C.R.,
Stevens B. R.,
Skimming J. W.,
Pan W. H. T.
Publication year - 2004
Publication title -
acta anaesthesiologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.738
H-Index - 107
eISSN - 1399-6576
pISSN - 0001-5172
DOI - 10.1111/j.1399-6576.2004.00454.x
Subject(s) - lipopolysaccharide , nitric oxide synthase , nitric oxide , medicine , isozyme , dexamethasone , pharmacology , biosynthesis , enzyme , lung , inflammation , endocrinology , biology , biochemistry
Background: Endotoxemia stimulates nitric oxide (NO) biosynthesis through induction of inducible NO synthase (iNOS). Cellular uptake of l ‐arginine, the sole substrate for iNOS, is an important mechanism regulating NO biosynthesis by iNOS. The isozymes of type‐2 cationic amino acid transporters, including CAT‐2, CAT‐2A, and CAT‐2B, constitute the most important pathways responsible for trans ‐membrane l ‐arginine transportation. Therefore, regulation of CAT‐2 isozymes expression may constitute one of the downstream regulatory pathways that control iNOS activity. We investigated the time course of enzyme induction and the role of nuclear factor‐κB (NF‐κB) in CAT‐2 isozymes expression in lipopolysaccharide‐(LPS) treated rat lungs. Methods: Adult male Sprague–Dawley rats were randomly given intravenous injections of normal saline (N/S), LPS, LPS plus NF‐κB inhibitor pre‐treatment (PDTC, dexamethasone, or salicylate), or an NF‐κB inhibitor alone. The rats were sacrificed at different times after injection and enzyme expression and lung injury were examined. Pulmonary and systemic NO production were also measured. Results: LPS co‐induced iNOS, CAT‐2, and CAT‐2B but not CAT‐2A expression in the lungs. Furthermore, NF‐κB actively participated in LPS‐induction of iNOS, CAT‐2, and CAT‐2B. LPS induced pulmonary and systemic NO overproduction and resulted in lung injuries. Attenuation of LPS‐induced iNOS, CAT‐2, and CAT‐2B induction significantly inhibited NO biosynthesis and lessened lung injury. Conclusion: NF‐κB actively participates in the induction of CAT‐2 and CAT‐2B in intact animals. Our data further support the idea that CAT‐2 and CAT‐2B are crucial in regulating iNOS activity.