Dithranol mediates pro-oxidative inhibition of polymorphonuclear leukocyte migration and lymphocyte proliferation
Autor: | U. Dippenaar, Pauline T. Lukey, Andre E. Nel, H. A. Eftychis, Ronald Anderson, G. H. Findlay, Marie W. Wooten |
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Rok vydání: | 1987 |
Předmět: |
Adult
Neutrophils Dermatology Lymphocyte proliferation Oxidative phosphorylation Pharmacology Lymphocyte Activation Dithranol medicine Humans Cells Cultured Protein Kinase C Protein kinase C Dose-Response Relationship Drug biology Cell growth Chemistry Biological activity Anthralin In vitro N-Formylmethionine Leucyl-Phenylalanine Chemotaxis Leukocyte Biochemistry Catalase Luminescent Measurements Leukocytes Mononuclear biology.protein Oxidation-Reduction medicine.drug |
Zdroj: | British Journal of Dermatology. 117:405-418 |
ISSN: | 1365-2133 0007-0963 |
DOI: | 10.1111/j.1365-2133.1987.tb04920.x |
Popis: | SUMMARY Dithranol (0.01–1 μg/ml), but not the auto-oxidized form, caused a dose-related enhancement of the generation of reactive oxidants by leukoattractant-activated polymorphonuclear leukocytes (PMNL) in vitro. At the same concentrations dithranol inhibited both PMNL migration to leukoattractants and mitogen-stimulated mononuclear leukocyte (MNL) proliferation. Catalase (50–100 units/ml) protected both PMNL migration and MNL proliferation from dithranol whilst ascorbate and cysteine (1 mM), which maintain dithranol in the biologically active reduced state, potentiated the inhibition. To establish the molecular mechanism of the pro-oxidative activity of dithranol its effects on cytosolic protein kinase C (PKC) activity were investigated. Dithranol caused a dose-related activation of PKC by apparent substitution for 1,2-diolein. These results demonstrate that dithranol, but not its auto-oxidation products, activates PKC which in turn initiates the generation of reactive oxidants by PMNL. Since reactive oxidants are immunosuppressive the therapeutic mechanisms of dithranol may be related to pro-oxidative interactions of this agent with skin phagocytes. |
Databáze: | OpenAIRE |
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