Title : Effect of methyl derivatives of dopamine on tumor necrosis factor alpha and lipid peroxidation.

Pub. Date : 2007 Dec

PMID : 18077578






6 Functional Relationships(s)
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1 We recently demonstrated that melatonin, N-acetylserotonin (NAS), and N-acetyldopamine (NAD) attenuate the synthesis of lipopolysaccharide (LPS)-stimulated tumor necrosis factor-alpha (TNF-alpha) and the generation of oxidant radicals. N-acetylserotonin tumor necrosis factor Homo sapiens
2 We recently demonstrated that melatonin, N-acetylserotonin (NAS), and N-acetyldopamine (NAD) attenuate the synthesis of lipopolysaccharide (LPS)-stimulated tumor necrosis factor-alpha (TNF-alpha) and the generation of oxidant radicals. N-acetylserotonin tumor necrosis factor Homo sapiens
3 We recently demonstrated that melatonin, N-acetylserotonin (NAS), and N-acetyldopamine (NAD) attenuate the synthesis of lipopolysaccharide (LPS)-stimulated tumor necrosis factor-alpha (TNF-alpha) and the generation of oxidant radicals. N-acetylserotonin tumor necrosis factor Homo sapiens
4 We recently demonstrated that melatonin, N-acetylserotonin (NAS), and N-acetyldopamine (NAD) attenuate the synthesis of lipopolysaccharide (LPS)-stimulated tumor necrosis factor-alpha (TNF-alpha) and the generation of oxidant radicals. N-acetylserotonin tumor necrosis factor Homo sapiens
5 Incubating THP-1-derived monocytes with rising concentrations of NAS, NAD, NMD, or 4-O-MD markedly decreased LPS-stimulated TNF-alpha production, which was dose dependent and on the order of 96%-98%. N-acetylserotonin tumor necrosis factor Homo sapiens
6 Our results indicated that the inhibitory effect of NAS, NAD, NMD, or 4-O-MD on LPS-induced TNF-alpha production and FeCl(2)-stimulated lipid peroxidation is robust and dose dependent. N-acetylserotonin tumor necrosis factor Homo sapiens