Cyclolinteinone, a sesterterpene from sponge Cacospongia linteiformis, prevents inducible nitric oxide synthase and inducible cyclo-oxygenase protein expression by blocking nuclear factor-κB activation in J774 macrophages
We investigated the effect of cyclolinteinone, a sesterterpene from Caribbean sponge Cacospongia linteiformis, mis, on inducible NO synthase (iNOS) and cyclo-oxygenase-2 (COX-?) protein expression in lipopolysaccharide (LPS)-stimulated J774 macrophages. Incubation of J774 cells with LPS (1 mu g/ml) caused an increase of both iNOS and COX-2 protein expression, which was prevented in a concentration-dependent fashion by cyclolinteinone (12.5, 25 and 50 mu M). Electrophoretic mobility-shift assay indicated that cyclolinteinone blocked the activation of nuclear factor-kappa B (NF-KB), a transcription factor necessary for either iNOS or COX-2 induction. Cyclolinteinone also blocked disappearance of I,B-cr from cytosolic fraction and nuclear translocation of NF-KB subunits p50 and p65. These results show that cyclolinteinone down-regulates iNOS and COX-2 protein expression by inhibiting NF-KB activation and suggest that it may represent a novel anti-inflammatory compound capable of controlling the excessive production of prostaglandins and nitric oxide occurring in several inflammatory diseases.
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
AUPHAN, N
DIDONATO, JA
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
DIDONATO, JA
ROSETTE, C
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
ROSETTE, C
HELMBERG, A
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
HELMBERG, A
KARIN, M
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
AUPHAN, N
DIDONATO, JA
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
DIDONATO, JA
ROSETTE, C
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
ROSETTE, C
HELMBERG, A
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA
HELMBERG, A
KARIN, M
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UNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USAUNIV CALIF SAN DIEGO, SCH MED,CTR GENET MOLEC,DEPT PHARMACOL, PROGRAM BIOMED SCI, LA JOLLA, CA 92093 USA