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Acta Academiae Medicinae Sinicae ; (6): 781-785, 2006.
Article in Chinese | WPRIM | ID: wpr-313685

ABSTRACT

<p><b>OBJECTIVE</b>To explore roles of extracellular signal-regulated kinase (ERK) 1/2, p38 mitogen activated protein kinase (p38 MAPK) and nuclear factor (NF) -KB in expression of inducible nitric oxide synthase (iNOS) in rat alveolar macrophages induced by high mobility group box 1 (HMGB1 ).</p><p><b>METHODS</b>Primary rat alveolar macrophages (PRAMs) cultured in vitro were incubated with PD98059 ( inhibitor against ERK), SB203580 (inhibitor against p38 MAPK) , PDTC (inhibitor against NF-kappaB), or PD98059 plus SB203580 for 2 hours, respectively. HMGB1 was added into the cultures and incubated with cells for 6 hours. Total RNA of PRAMs was extracted and iNOS mRNA expression was semi-quantified with reverse transcription-polymerase chain reaction ( RT-PCR). Greiss reaction was applied to determine nitrite/nitrate (NO2-/NO3- ) concentration in PRAMs culture supernatants.</p><p><b>RESULTS</b>Expression of iNOS mRNA and NO production in PRAMs culture supernatants were down-regulated by inhibition of ERK or p38 MAPK by PD98059 or SB203580, respectively (P <0. 05). Moreover, inhibition of iNOS expression and NO production was observed after simultaneous pretreatment with PD98059 and SB203580 (P < 0. 05). Expression of iNOS mRNA in PRAMs and NO production in PRAMs culture supernatants were down-regulated by inhibition of NF-kappaB by PDTC (P <0. 05).</p><p><b>CONCLUSION</b>Cellular signal molecules of ERK, p38 MAPK, and NF-kappaB all participate in the expression of iNOS and NO production in PRAMs induced by HMGB1.</p>


Subject(s)
Animals , Male , Rats , Cells, Cultured , Extracellular Signal-Regulated MAP Kinases , Physiology , Flavonoids , Pharmacology , HMGB1 Protein , Pharmacology , Imidazoles , Pharmacology , Macrophages, Alveolar , Metabolism , NF-kappa B , Physiology , Nitric Oxide Synthase Type II , Proline , Pharmacology , Pyridines , Pharmacology , RNA, Messenger , Rats, Sprague-Dawley , Signal Transduction , Thiocarbamates , Pharmacology , p38 Mitogen-Activated Protein Kinases , Physiology
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