大豆异黄酮对β淀粉样肽诱导的大鼠脑组织炎症相关因子表达的影响
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R735.1

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国家自然科学基金( 30972470);北京市自然科学基金


Effect of soybean isoflavones on the expression of inflammatory mediators in the brain of rats induced by p_amyloid peptides
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    摘要:

    目的研究大豆异黄酮( SIF)对p淀粉样肽1-42( A[31-42)诱导的大鼠脑炎症损伤的作用。方法将健 康雄性Wistar大鼠按体重随机分成对照组、Ap模型组,SIF干预组(SIF+ A[3组)和SIF组(SIF单独处理组)。SIF 干预组和SIF组大鼠每日给予大豆异黄酮(80 m~kg)灌胃处理,共14 d。然后A[3模型组和SIF干预组采用微型注 射泵在大鼠侧脑室区持续注射A[31-42 14 d,建立大鼠脑炎症损伤模型。采用RT-PCR方法和Western blot方法检 测脑组织白介素一1p(11-1p)、诱导型一氧化氮合成酶(iNOS)以及白介素-10(IL-10)基因和蛋白水平的表达。结果 与模型组比较,SIF干预组大鼠脑组织11-1[3、iNOS及IL-10基因和蛋白表达水平显著下调(P<0.05)。结论 大 豆异黄酮可能是通过影响大鼠腑组织炎症相关因子及酶基因/蛋白水平的表达来拮抗A3142介导的脑炎症反应。

    Abstract:

    Objective To investigate the protective mec,hanism of soybean isoflavones ( SIF) against the inflammatory impairment in the brain of rats induced by [3-amyloid peptidel-42 (A[31-42). Methods Based on the body weight of rats, 32 healthy Wistar rats ( male, aged 3 months) were randomly divided into four groups ( control, A[3, SIF +A[3 and SIF groups). The inflammatory impairment model was established by injecting A[3142 (10肛g) into the lateral cerebral ve,ntricle of rats with micropump for 14 days. The rats in SIF + A[3 and SIF groups were treatecl with SIF ( 80 mg/kg bw) per day by gavaging for 14 days before the injection of A[3, while the rats in control group and A[3 group were treated with 0.5 % CMC-Na. On the 15'h day after A[3 injection, the rats were killed for the mRNA and protein expression of interleukin-1[3 ( 11-1 [3) , inducible nitric oxide synthase ( iNOS) and interleukin-10 ( IL-10) in brain tissue tested hy RT- PCR and western blot. Results Comparing with the A[3 group, the mRNA and protein expression of IL-1[3, iNOS and IL- 10 0f SIF treated groups were decreased significantly ( P < 0. 05). Conclusion The expression of IL-1[3, iNOS ancl IL-10 at gene and peotein level could be down-regulated by soy isoflavones, therefore the inflammatory damage induc:ed by A[31- 42 was inhibitd.

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周新,丁冰杰,肖荣,苑林宏,麻微微,余焕玲,席元第,丁娟,封锦芳.大豆异黄酮对β淀粉样肽诱导的大鼠脑组织炎症相关因子表达的影响[J].中国食品卫生杂志,2012,24(1):1-4.

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