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α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)可预防培养的小脑颗粒细胞神经元中谷氨酸诱导的神经毒性和细胞凋亡。

AMPA prevents glutamate-induced neurotoxicity and apoptosis in cultured cerebellar granule cell neurons.

作者信息

Banaudha K, Marini A M

机构信息

Department of Neurology, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA.

出版信息

Neurotox Res. 2000;2(1):51-61. doi: 10.1007/BF03033327.

Abstract

Exposure of cultured cerebellar neurons to alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) in the presence of aniracetam protects all of the vulnerable neurons against the excitotoxic actions of glutamate acting on N-methyl-D-aspartate receptors. The protective effect of AMPA was both time- and concentration-dependent. Aniracetam alone did not protect the neurons against the excitotoxic effects of glutamate. Pretreatment of cerebellar neurons with the AMPA antagonist, 6-cyano-7-nitroquinoxaline-2,3-dione blocked the neuroprotective effect mediated by AMPA indicating that the neuroprotective effect is mediated specifically by AMPA receptors. An excitotoxic concentration of glutamate, which killed between 60-80% of granule cell neurons on day 8 in vitro, mediated its toxic effect via a time-dependent apoptotic pathway. Pretreatment of cerebellar granule cell neurons with AMPA (500 microM) completely blocked glutamate-mediated apoptosis. Our results suggest that AMPA receptors may play an important role in neuronal survival.

摘要

在茴拉西坦存在的情况下,将培养的小脑神经元暴露于α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)中,可保护所有易损神经元免受谷氨酸作用于N-甲基-D-天冬氨酸受体所产生的兴奋性毒性作用。AMPA的保护作用具有时间和浓度依赖性。单独使用茴拉西坦不能保护神经元免受谷氨酸的兴奋性毒性作用。用AMPA拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮预处理小脑神经元可阻断AMPA介导的神经保护作用,这表明神经保护作用是由AMPA受体特异性介导的。谷氨酸的兴奋性毒性浓度在体外第8天可杀死60%-80%的颗粒细胞神经元,其毒性作用通过时间依赖性凋亡途径介导。用AMPA(500微摩尔)预处理小脑颗粒细胞神经元可完全阻断谷氨酸介导的凋亡。我们的结果表明,AMPA受体可能在神经元存活中起重要作用。

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