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首页> 外文期刊>Journal of Traditional Chinese Medical Sciences >Glycyrrhiza uralensis flavonoids inhibit brain microglial cell TNF-α secretion, p-IκB expression, and increase brain-derived neurotropic factor (BDNF) secretion
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Glycyrrhiza uralensis flavonoids inhibit brain microglial cell TNF-α secretion, p-IκB expression, and increase brain-derived neurotropic factor (BDNF) secretion

机译:乌拉尔甘草类黄酮抑制脑小胶质细胞TNF-α分泌,p-IκB表达并增加脑源性神经营养因子(BDNF)的分泌

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摘要

Objective Asthma sufferers exhibit high prevalence of anxiety/depression. Elevated tumor-necrosis factor-alpha (TNF-α) levels in peripheral system and central nervous system (CNS) are associated with anxiety/depression, whereas brain-derived neurotropic factor (BDNF) has anti-depressant effects. An anti-asthma herbal medicine intervention ASHMI inhibits peripheral TNF-α secretion in an animal model of asthma. We hypothesize that ASHMI and its compounds may have modulatory effects on CNS TNF-α and BDNF production. We sought to determine the effect of ASHMI and individual herb constituents on brain microglial cell TNF-α production, and identify the active compounds that suppress TNF-α and increase BDNF. Methods BV-2 mouse microglial cells were pre-treated with ASHMI or extracts of Ganoderma lucidum ( G. lucidum) , Sophora flavescens Ait ( S. flavescens) , and Glycyrrhiza uralensis Fischer ( G. uralensis) , the herbal constituents in ASHMI, or individual compounds isolated from G. uralensis at different concentrations and then stimulated with LPS. TNF-α levels in culture supernatants were measured by ELISA. The effect of active compounds on NFκB signaling pathway and on BDNF production were determined by western blotting and ELISA, respectively. Results ASHMI produced dose-dependent inhibition of TNF-α secretion by cultured-mouse microglia BV2 cells. Of the three herb extracts in ASHMI, only G. uralensis significantly and dose-dependently inhibited TNF-α production. Among the 5 flavonoids isolated from G. uralensis , isoliquiritigenin was the most effective. Isoliquiritigenin suppression of TNF-α production was associated with attenuation of p-NF-κB expression, and was accompanied by increased BDNF secretion. Conclusion ASHMI and its effective flavonoid, isoliquiritigenin, inhibited TNF-α production by LPS stimulated microglial cells and elevated BDNF levels, which may prove to have anti-CNS inflammatory and anti-anxiety effects.
机译:目的哮喘患者表现出很高的焦虑/抑郁感。周围系统和中枢神经系统(CNS)的肿瘤坏死因子-α(TNF-α)水平升高与焦虑/抑郁相关,而脑源性神经营养因子(BDNF)具有抗抑郁作用。抗哮喘草药干预ASHMI可以抑制哮喘动物模型中外周TNF-α的分泌。我们假设ASHMI及其化合物可能对CNSTNF-α和BDNF产生有调节作用。我们试图确定ASHMI和单个草药成分对脑小胶质细胞TNF-α产生的影响,并确定抑制TNF-α和增加BDNF的活性化合物。方法用ASHMI或灵芝提取物flavescens Ait(flavescens)和Glycyrrhiza uralensis Fischer提取物(G. uralensis)或ASHMI预处理BV-2小鼠小胶质细胞。从甘草中分离出不同浓度的各种化合物,然后用LPS刺激。通过ELISA测量培养上清液中的TNF-α水平。分别通过蛋白质印迹和ELISA确定活性化合物对NFκB信号传导途径和对BDNF产生的影响。结果ASHMI产生了小鼠小胶质细胞BV2细胞对TNF-α分泌的剂量依赖性抑制作用。在ASHMI中的三种草药提取物中,仅G. uralensis显着且剂量依赖性地抑制TNF-α的产生。在从甘草中分离出的5种黄酮中,异黄体生成素最有效。异寡糖原蛋白抑制TNF-α的产生与p-NF-κB表达的减弱有关,并伴有BDNF分泌增加。结论ASHMI及其有效的类黄酮异黄体生成素可抑制LPS刺激的小胶质细胞产生的TNF-α,并增加BDNF的水平,这可能证明具有抗中枢神经系统的炎症和抗焦虑作用。

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