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Radioprotective effect of ursolic acid in radiation-induced impairment of neurogenesis, learning and memory in adolescent BALB/c mouse

机译:熊酸在辐射诱导的辐射诱导神经发生,学习和记忆中的辐射保护作用,青少年BALB / C小鼠的损伤

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The effect of acute irradiation with 5 Gy or fractionated exposure with 0.5 Gy continuously for 10 days (a total dose of 5 Gy) was evaluated in an immature BALB/c mouse model. Radioprotective effect of ursolic acid (at 25 mg/kg/daily administered 1 h after acute or each of fractionated irradiations, and continuously for 30 days) was also investigated. We found that both acute and fractionated irradiation at a total dose of 5 Gy did not induce any mortality within 30 days after exposure to postnatal day 26 (P26) BALB/c mice, but reduced animal weigh gain in the first few weeks. At 90 days after irradiation, the weight of animals with acute irradiation was still significantly lower than the control group; no significant difference though was observed for those fractionatedly exposed mice compared to the control group. Behavioral tests indicated that acute irradiation at 5 Gy induced deficits in learning and memory in the contextual fear conditioning test. The memory for novel object recognition was also impaired. Similar changes were not observed in mice with fractionated irradiation. Immunohistochemical study demonstrated clearly that acute and fractionated irradiations induced impairment of neurogenesis in the subgranular zone (SGZ) of the dentate gyrus although fractionated exposure induced much lesser loss of newly generated neurons. Ursolic acid administered at 25 mg/kg/daily for 30 days after irradiation greatly improved acute irradiation-induced deficits in contextual learning and memory and in novel object recognition memory although it exacerbated radiation-induced reduction of neurogenesis in SGZ.
机译:在未成熟的BALB / C小鼠模型中,评价急性辐照5μm或分馏出0.5Gy的曝光效果10天(总剂量为5GY)。还研究了熊磷酸的辐射保护作用(急性或每种分级照射后25mg / kg /每日施用1小时,并连续30天)。我们发现,急性和分馏的辐照在暴露于产后第26天(P26)BALB / C小鼠后30天内没有在30天内诱导任何死亡率,但在最初几周内减少了动物称重增益。辐照后90天,急性辐照动物的重量仍明显低于对照组;与对照组相比,对于那些分级暴露的小鼠没有观察到显着差异。行为试验表明,在语境恐惧调理试验中,5 GY的急性辐照诱导学习和记忆中的缺陷。新的对象识别的记忆也被损害。小鼠中未观察到类似的变化,分离辐射。免疫组织化学研究显然明确表明,急性和分馏的照射诱导神经发生在齿状区(SGZ)中神经发生的损害,尽管分馏出暴露诱导新产生的神经元的损失更小。在照射后,在25mg / kg /每日施用30天,在辐射大大提高了急性辐照引起的上下文学习和记忆中的缺陷,并且在新的对象识别记忆中,尽管它加剧了辐射诱导的辐射诱导的神经发生在SGZ中的降低。

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