Inhibitory effects of nitric oxide and interleukin-10 on production of tumor necrosis factor alpha, interleukin-1 beta, and interleukin-6 in mouse alveolar macrophages
Hb. Qiu et al., Inhibitory effects of nitric oxide and interleukin-10 on production of tumor necrosis factor alpha, interleukin-1 beta, and interleukin-6 in mouse alveolar macrophages, ACT PHAR SI, 20(3), 1999, pp. 271-275
AIM: To observe the effects of nitric oxide and interleukin-10 (IL-10) on i
nflammatory reaction in mouse alveolar macrophages ( AM). METHODS: AM from
mice were stimulated by lipopolysaccharides (LPS) 10 mg . L-1 and nitric-ox
ide synthase inhibitor, S-methylisothiorea sulfate (SMT) or nitric-oxide do
nor, S-nitroso-N-acetyl-D, L-penicillamine ( SNAP). The production of tumor
necrosis factor alpha (TNF alpha), IL-1 beta, IL-6, and IL-10 by AM were m
easured by ELISA. RESULTS: After LPS-stimulation, TNF alpha, IL-1 beta, and
IL-6 peaked at 6, 12, and 24 h, respectively by AM. SMT inhibited LPS-indu
ced nitric oxide release and increased IL-1 beta and IL-6 secretions in AM,
but the TNF alpha levels remained unchanged. SNAP had inhibitory effects o
n IL-1 beta and IL-6 secretions ina concentration-dependent manner, but exe
rted no effect on TNF alpha release. TNF alpha, IL-1 beta, and IL-6 secreti
ons were inhibited by recombinant IL-10, but the cytokines release was upre
gulated by anti-IL-10 monoclonal antibody. CONCLUSION: Both endogenous and
exogenous nitric oxide and IL-10 had inhibitory effects on the LPS-induced
TNF alpha, IL-1 beta, and IL-6 secretions in mouse AM.