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多奈哌齐对暴露于 N-甲基-D-天冬氨酸(NMDA)毒性的原代培养大鼠皮质神经元的保护作用。

Protective effect of donepezil in primary-cultured rat cortical neurons exposed to N-methyl-d-aspartate (NMDA) toxicity.

作者信息

Akasofu Shigeru, Kimura Manami, Kosasa Takashi, Ogura Hiroo, Sawada Kohei

机构信息

Tsukuba Research Laboratories, Eisai Co., Ltd. 5-1-3 Tokodai, Tsukuba-shi, Ibaraki 300-2635, Japan.

出版信息

Eur J Pharmacol. 2006 Jan 20;530(3):215-22. doi: 10.1016/j.ejphar.2005.11.057.

Abstract

Donepezil has a neuroprotective effect against oxygen-glucose deprivation injury and glutamate toxicity in cultured cortical neurons. In this study, we further characterized the neuroprotective properties of donepezil in rat cortical cell cultures using glutamate receptor-specific agonists (N-methyl-d-aspartate (NMDA), alpha-amino-3-hydroxy-5-methylisoxazolepropionate (AMPA) and kainate). Pretreatment with donepezil (1 microM) for 12 h significantly decreased the lactate dehydrogenase (LDH) release in response to NMDA (100 microM) by 43.8%, and reduced the LDH release in response to kainate (100 microM) and AMPA (100 microM) by 11.9% and 7.5% (without statistical significance), respectively. Donepezil appeared to inhibit LDH release in a concentration-dependent manner at 0.1-10 microM. Cortical neurons exposed to NMDA retained a normal morphological appearance in the presence of 10 microM donepezil. In binding assay for glutamate receptors, donepezil at 100 microM only slightly inhibited binding to the glycine and polyamine sites on NMDA receptor complex. On the other hand, 12 h pretreatment with donepezil at 10 and 100 microM significantly decreased the NMDA-induced increase of intracellular calcium concentration ([Ca2+]i). In conclusion, our results show that donepezil has protective activity against NMDA toxicity in cortical neurons, and this neuroprotection seems to be partially mediated by inhibition of the increase of [Ca2+]i.

摘要

多奈哌齐对培养的皮质神经元的氧-葡萄糖剥夺损伤和谷氨酸毒性具有神经保护作用。在本研究中,我们使用谷氨酸受体特异性激动剂(N-甲基-D-天冬氨酸(NMDA)、α-氨基-3-羟基-5-甲基异恶唑丙酸(AMPA)和海人酸)进一步表征了多奈哌齐在大鼠皮质细胞培养物中的神经保护特性。用多奈哌齐(1μM)预处理12小时可使对NMDA(100μM)反应的乳酸脱氢酶(LDH)释放显著降低43.8%,并使对海人酸(100μM)和AMPA(100μM)反应的LDH释放分别降低11.9%和7.5%(无统计学意义)。多奈哌齐在0.1-10μM时似乎以浓度依赖性方式抑制LDH释放。在存在10μM多奈哌齐的情况下,暴露于NMDA的皮质神经元保持正常形态外观。在谷氨酸受体结合试验中,100μM的多奈哌齐仅轻微抑制与NMDA受体复合物上甘氨酸和多胺位点的结合。另一方面,用10和100μM的多奈哌齐预处理12小时可显著降低NMDA诱导的细胞内钙浓度([Ca2+]i)升高。总之,我们的结果表明,多奈哌齐对皮质神经元中的NMDA毒性具有保护活性,并且这种神经保护作用似乎部分是通过抑制[Ca2+]i升高来介导的。

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