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参与 microRNA 124-CREB 通路:益智标准提取物(BESEB CDRI-08)增强平行记忆的平行机制。

Participation of microRNA 124-CREB pathway: a parallel memory enhancing mechanism of standardised extract of Bacopa monniera (BESEB CDRI-08).

机构信息

Department of Animal Science, School of Life Sciences, Bharathidasan University, Tiruchirappalli 620024, India.

出版信息

Neurochem Res. 2012 Oct;37(10):2167-77. doi: 10.1007/s11064-012-0840-z. Epub 2012 Jul 27.

Abstract

Bacosides, the effective component of standardised leaf extract of Bacopa monniera (BESEB CDRI-08) has been reported to have memory enhancing effect. Our previous reports suggested that BESEB CDRI-08 (BME) improves memory in postnatal rats by enhancing serotonin [5-hydroxytryptamine (5-HT)] metabolism, its transportation and subsequently activates 5-HT(3A) receptor during hippocampus-dependent learning. In this study, we examine whether the up-regulated 5-HT(3A) receptor activity by BME modulate microRNA 124-CREB pathway to enhance synaptic plasticity. Wistar rat pups received single dose of vehicle solution (0.5 % gum acacia + 0.9 % saline)/BME (80 mg/kg)/mCPBG (10 mg/kg)/BME + mCPBG during the postnatal days (PND) 15-29. On PND 30, individuals were trained at brightness discrimination task and 24 h later, they were tested on the task. The BME treated group exhibited significantly lower percentage of errors during retention than acquisition. In addition, pre-miR-124 expression in hippocampus was significantly down-regulated in the BME and mCPBG + BME treated groups combined with a significant increase in the plasticity related genes, cAMP response element-binding protein, its phosphorylation and postsynaptic density protein 95. Our results suggest that this may be one of the mechanisms of bacosides present in BME for the memory enhancement.

摘要

Bacosides 是益智草(Bacopa monniera)标准化叶提取物(BESEB CDRI-08)的有效成分,已被报道具有增强记忆的作用。我们之前的报告表明,BESEB CDRI-08(BME)通过增强 5-羟色胺(5-HT)代谢、转运,随后在海马依赖性学习过程中激活 5-HT(3A)受体,从而改善产后大鼠的记忆。在这项研究中,我们研究了 BME 上调的 5-HT(3A)受体活性是否通过调节 microRNA 124-CREB 通路来增强突触可塑性。Wistar 幼鼠在产后第 15-29 天接受单剂量的载体溶液(0.5%树胶阿拉伯胶+0.9%生理盐水)/BME(80mg/kg)/mCPBG(10mg/kg)/BME+mCPBG。在 PND 30 天,个体在亮度辨别任务中接受训练,24 小时后在任务中进行测试。BME 处理组在保留期间的错误百分比明显低于获得期间。此外,BME 和 mCPBG+BME 处理组的海马体中的前 microRNA-124 表达明显下调,与可塑性相关基因 cAMP 反应元件结合蛋白、其磷酸化和突触后密度蛋白 95 的显著增加相结合。我们的结果表明,这可能是 BME 中存在的 bacosides 增强记忆的机制之一。

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