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首页> 外文期刊>Neural regeneration research >Geniposide, the component of the Chinese herbal formula Tongluojiunao, protects amyloid-β (Aβ)1-42-mediated death of hippocampal neurons via the non-classical estrogen signaling pathway
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Geniposide, the component of the Chinese herbal formula Tongluojiunao, protects amyloid-β (Aβ)1-42-mediated death of hippocampal neurons via the non-classical estrogen signaling pathway

机译:ip子苷是中药通络九脑的成分,可通过非经典的雌激素信号通路保护β-淀粉样蛋白(Aβ)1-42介导的海马神经元死亡。

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摘要

Tongluojiunao (TLJN) is an herbal medicine consisting of two main components, geniposide and ginsenoside Rg1. TLJN has been shown to protect primary cultured hippocampal neurons. However, its mechanism of action remains unclear. In the present study, primary cultured hippocampal neurons treated with Aβ1-42 (10 μmol/L) significantly increased the release of lactate dehydrogenase, which was markedly reduced by TLJN (2 μL/mL), specifically by the component geniposide (26 μmol/L), but not ginsenoside Rg1 (2.5 μmol/L). The estrogen receptor inhibitor, ICI182780 (1 μmol/L), did not block TLJN- or geniposide-mediated decrease of lactate dehydrogenase under Aβ1-42-exposed conditions. However, the phosphatidyl inositol 3-kinase or mitogen-activated protein kinase pathway inhibitor, LY294002 (50 μmol/L) or U0126 (10 μmol/L), respectively blocked the decrease of lactate dehydrogenase mediated by TLJN or geniposide. Therefore, these results suggest that the non-classical estrogen pathway (i.e., phosphatidyl inositol 3-kinase or mitogen-activated protein kinase) is involved in the neuroprotective effect of TLJN, specifically its component, geniposide, against Aβ1-42-mediated cell death in primary cultured hippocampal neurons.
机译:通络九脑(TLJN)是一种由子苷和人参皂苷Rg1两个主要成分组成的草药。 TLJN已被证明可以保护原代培养的海马神经元。但是,其作用机理仍不清楚。在本研究中,经Aβ 1 - 42 (10μmol/ L)处理的原代培养海马神经元显着增加了乳酸脱氢酶的释放,而TLJN明显降低了乳酸脱氢酶的释放。 2μL/ mL),特别是by子苷(26μmol/ L),而不是人参皂苷Rg1(2.5μmol/ L)。在暴露于Aβ 1 - 42 的条件下,雌激素受体抑制剂ICI182780(1μmol/ L)不会阻止TLJN或子苷介导的乳酸脱氢酶的减少。然而,磷脂酰肌醇3-激酶或丝裂原激活的蛋白激酶途径抑制剂LY294002(50μmol/ L)或U0126(10μmol/ L)分别阻止了TLJN或子苷介导的乳酸脱氢酶的减少。因此,这些结果表明非经典的雌激素途径(即磷脂酰肌醇3-激酶或丝裂原激活的蛋白激酶)参与了TLJN的神经保护作用,特别是其成分子苷对Aβ 1 的保护作用。 sub>- 42 介导的原代培养海马神经元细胞死亡。

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