首页> 外文期刊>Basic & clinical pharmacology & toxicology. >Effect of tetrandrine on calcium-dependent tumour necrosis factor-alpha production in glia-neurone mixed cultures.
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Effect of tetrandrine on calcium-dependent tumour necrosis factor-alpha production in glia-neurone mixed cultures.

机译:粉防己碱对神经胶质-神经元混合培养物中钙依赖性肿瘤坏死因子-α产生的影响。

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Tumour necrosis factor-alpha is believed to have a deleterious role in the pathophysiology of brain injury. Tetrandrine has protective effect on neuronal cells, however, the mechanisms involved in its action have not been clearly established. The aim of this study was to investigate the role of tetrandrine on calcium-dependent tumour necrosis factor-alpha production in glia-neurone mixed cultures. Glia-neurone mixed cultures were treated by addition of Ca2+ regulating agents for a period of 6 hr. Tetrandrine or/and TMB-8 were added 30 min. before the stimulation. The supernatant tumour necrosis factor-alpha levels were quantified by enzyme-linked immunosorbent assay. Exposure of lipopolysaccharide 10 and 100 ng/ml caused significant increase in tumour necrosis factor-alpha production respectively, with no alteration in cultures treated with 1 ng/ml lipopolysaccharide. Glia-neurone mixed cultures exhibited a marked elevation in tumour necrosis factor-alpha production after exposure to CaCl2, KCl, thapsigargin, BHQ and norepinephrine in the presence of lipopolysaccharide at 1 ng/ml respectively. Tetrandrine 0.3, 1, and 3 microM concentration-dependently reduced tumour necrosis factor-alpha production evoked by CaCl2 or KCl. Tetrandrine preincubation had no significant effect on the response to Ca2+-ATPase inhibitor thapsigargin or BHQ. Norepinephrine-induced tumour necrosis factor-alpha production was significantly reduced by tetrandrine and almost abolished by combination of tetrandrine and intracellular Ca2+ release inhibitor TMB-8. These results suggested that tetrandrine at a concentration of 0.3, 1, or 3 microM inhibited tumour necrosis factor-alpha production induced by Ca2+ entry in glia-neurone mixed cultures.
机译:肿瘤坏死因子-α被认为在脑损伤的病理生理学中具有有害作用。粉防己碱对神经元细胞具有保护作用,但是,尚不清楚其作用所涉及的机制。这项研究的目的是调查粉防己碱在神经胶质-神经元混合培养物中对钙依赖性肿瘤坏死因子-α产生的作用。通过添加Ca 2+调节剂处理胶质神经元混合培养物6小时。加入30min的粉防己碱或/和TMB-8。在刺激之前。通过酶联免疫吸附测定法定量上清液中的肿瘤坏死因子-α水平。脂多糖10和100 ng / ml的暴露分别导致肿瘤坏死因子-α的产生显着增加,而用1 ng / ml脂多糖处理的培养物中无变化。分别在1 ng / ml的脂多糖存在下,暴露于CaCl2,KCl,毒胡萝卜素,BHQ和去甲肾上腺素后,神经胶质神经元混合培养物的肿瘤坏死因子-α产生显着升高。粉防己碱0.3、1和3 microM浓度依赖性地降低了CaCl2或KCl引起的肿瘤坏死因子-α的产生。粉防己碱预温育对Ca2 + -ATPase抑制剂毒胡萝卜素或BHQ的反应无明显影响。粉防己碱可显着降低去甲肾上腺素诱导的肿瘤坏死因子-α的产生,而粉防己碱和细胞内Ca2 +释放抑制剂TMB-8的组合可将其几乎消除。这些结果表明,浓度为0.3、1或3 microM的粉防己碱抑制了由胶质神经元混合培养物中Ca2 +进入引起的肿瘤坏死因子-α的产生。

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