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OBJECTIVE To investigate the protective effect of Noble dendrobium polysaccharides(NDP) on inflammatory factors,which are produced and released by 1ipopolysaecharide(LPS)-activated rat cerebral microglia,and to explore the protective mechanisms of NDP against LPS-induced neuron damage.METHODS The whole brains of 1 or 2-day-old mice was dissected,and microglia were isolated and cultured.Before exposure to LPS neurotoxicity,cells were treated with NDP(24 h),and the microglia-conditioned medium(MCM) collected.Primary neuronal cultures were supplemented with the 24 h MCM.The morphology and density of neuronal synapses were observed by immunofluorescence;the production of NO was detected with the Griess reagent;the level of tumor necrosis factor-α(TNF-α) was assessed by ELISA;the degree of neuronal apoptosis was examined with Hoechst 33258.RESULTS The hippocampal neurons were apparently damaged by the supernatant of activated MCM,and the morphology of the neurons changed significantly.Compared to control group,the level of NO was elevated and the expression level of TNF-α protein was significantly increased,and the apoptosis was induced in neurons.NDP improved synaptic morphology and increase synapses density,depress the high-level of NO,inhibited the up-expression of TNF-α protein by LPS,and decreased neuronal apoptosis.CONCLUSION NDP may significantly inhibit the activation of microglia induced by LPS and reduce the release of inflammatory factors.These results showed that NDP exert neuroprotection through depressing the actived microglia.
OBJECTIVE To investigate the protective effect of Noble dendrobium polysaccharides (NDP) on inflammatory factors, which were produced and released by 1ipopolysaecharide (LPS) -activated rat cerebral microglia, and to explore the protective mechanisms of NDP against LPS-induced neuron damage. METHODS The whole brains of 1 or 2-day-old mice were dissected, and microglia were isolated and cultured. Before exposure to LPS neurotoxicity, cells were treated with NDP (24 h), and the microglia-conditioned medium (MCM) collected. Primary neuronal cultures were supplemented with the 24 h MCM.The morphology and density of neuronal synapses were observed by immunofluorescence; the production of NO was detected with the Griess reagent; the level of tumor necrosis factor-α (TNF-α) was assessed by ELISA; the degree of neuronal apoptosis was examined with Hoechst 33258.RESULTS The hippocampal neurons were apparently damaged by the supernatant of activated MCM, and the morphology of the neurons changed significantly.Com pared to control group, the level of NO was elevated and the expression level of TNF-α protein was significantly increased, and the apoptosis was induced in neurons. NPD improved synaptic morphology and increase synapses density, depress the high-level of NO, inhibited the up-expression of TNF-alpha protein by LPS, and decreased neuronal apoptosis. CONCLUSION NDP may significantly inhibit the activation of microglia induced by LPS and reduce the release of inflammatory factors. These results showed that NDP exert neuroprotection through depressing the actived microglia.