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Neuroimmunomodulation ; 11(2): 127-32, 2004.
Article in English | MEDLINE | ID: mdl-14758059

ABSTRACT

OBJECTIVES: Recent reports point to a role for the nitric oxide/nitric oxide synthase (NO/NOS) system in implantation. It has been suggested that inducible NOS expressed at peri-implantation would lead to enhanced NO production, which could promote the attachment of the blastocyst. Short-term administration of NO donors during the pre-implantation period reduced the pregnancy rate in a dose-dependent manner. Thus, it is thought that optimal levels of NO are critical for embryo implantation, so regulation of NOS must be crucial. Taking this into consideration, interleukin-10 (IL-10), synthesized and secreted by the embryo, could be modulating NOS during implantation. In this study we have investigated the in vitro effect of IL-10 on NOS in the uterus. METHODS: To determine the effect of IL-10, slices of uterus from estrogenized mice were pre-incubated for 60 min with different concentrations of IL-10 and NOS activity was measured. RESULTS: IL-10 (50 and 100 ng/ml in vitro) diminished NOS activity. The in vivo administration of lipopolysaccharide (LPS; 8 mg/kg) significantly increased the conversion of arginine into citrulline. This effect was abolished after 60 min of preincubation with IL-10 (100 ng/ml). The stimulatory effect of LPS and estrogen on NOS activity is exerted on the Ca-independent isoform and IL-10 in vitro abolished this increase. We observed that the uterus of pregnant mice on day 5 of gestation synthesized NO. This production was significantly inhibited by preincubation with IL-10 (100 ng/ml). CONCLUSIONS: This report demonstrates that IL-10 is capable of inhibiting NO synthesis in estrogenized, LPS-treated and pregnant rat uterus.


Subject(s)
Interleukin-10/metabolism , Nitric Oxide Synthase/biosynthesis , Nitric Oxide/biosynthesis , Uterus/enzymology , Animals , Arginine/metabolism , Citrulline/biosynthesis , Dose-Response Relationship, Drug , Down-Regulation/drug effects , Down-Regulation/immunology , Estrogens/metabolism , Estrogens/pharmacology , Female , Interleukin-10/immunology , Interleukin-10/pharmacology , Lipopolysaccharides/pharmacology , Mice , Mice, Inbred BALB C , Nitric Oxide Synthase/drug effects , Pregnancy , Uterus/drug effects , Uterus/immunology
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