1. Leishmania (L.) amazonensis-induced inhibition of nitric oxide synthesis in host macrophages.
- Author
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Balestieri FM, Queiroz AR, Scavone C, Costa VM, Barral-Netto M, and Abrahamsohn Ide A
- Subjects
- Animals, Cells, Cultured, Lipopolysaccharides pharmacology, Macrophages drug effects, Macrophages metabolism, Mice, Nitric Oxide Synthase genetics, Nitric Oxide Synthase metabolism, Nitric Oxide Synthase Type II, RNA, Messenger genetics, RNA, Messenger metabolism, Leishmania pathogenicity, Leishmaniasis parasitology, Macrophages parasitology, Nitric Oxide biosynthesis
- Abstract
Inhibition of lipopolysaccharide (LPS)-induced nitric oxide (NO) production was demonstrated in J774-G8 macrophages infected with Leishmania (L.) amazonensis promastigotes. The downmodulation of NO production observed in infected and LPS-stimulated J774-G8 cells correlated with a reduction in inducible nitric oxide synthase (iNOS) activity. Reduction in iNOS activity was not paralleled by decreased iNOS mRNA expression, suggesting that the parasite affects post-transcriptional events of NO synthesis. Supplementation with L-arginine or tetrahydrobiopterin did not increase NO production, suggesting that inhibition is not due to an insufficiency of substrate or co-factor. Treatment with anti-IL-10, anti-IL-4 or anti-TGF-beta neutralizing antibodies also failed to increase NO production, indicating that these cytokines are not involved in the observed parasite-induced inhibition of NO synthesis. However, treatment of the cultures with IFN-gamma resulted in a marked increase in NO production by infected LPS-stimulated cells. These results show that although L.(L.) amazonensis infection inhibits iNOS activity and NO production by J774-G8 cells, activation by IFN-gamma is capable of overriding the suppression of NO synthesis.
- Published
- 2002
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