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丙酮酸和苹果酸对谷氨酸介导的神经毒性的保护作用。

Protection by pyruvate and malate against glutamate-mediated neurotoxicity.

作者信息

Ruiz F, Alvarez G, Pereira R, Hernández M, Villalba M, Cruz F, Cerdán S, Bogónez E, Satrústegui J

机构信息

Departamento de Biología Molecular, Centro de Biología Molecular Severo Ochoa, Universidad Autónoma de Madrid, Spain.

出版信息

Neuroreport. 1998 May 11;9(7):1277-82.

PMID:9631412
Abstract

Pyruvate and malate (P/M) increase the contribution of mitochondria to neuronal calcium homeostasis. We have now found that cortical neuronal cultures utilize pyruvate preferentially over glucose. The supply of pyruvate and malate protects hippocampal and cortical neurons against delayed cell death occurring 24 h after glutamate exposure. High [Ca2+]i levels attained during and after glutamate exposure were reduced when neurons were incubated in the presence of P/M. At the single cell level, this was reflected in a decrease in the number of neurons that respond to glutamate with high rises in [Ca2+]i. The results suggest that the ability to prevent large increases in [Ca2+]i may underlie the beneficial effects of pyruvate and malate during glutamate excitotoxicity.

摘要

丙酮酸和苹果酸(P/M)增加了线粒体对神经元钙稳态的贡献。我们现在发现,皮质神经元培养物优先利用丙酮酸而非葡萄糖。丙酮酸和苹果酸的供应可保护海马体和皮质神经元免受谷氨酸暴露后24小时发生的延迟性细胞死亡。当神经元在P/M存在的情况下孵育时,谷氨酸暴露期间及之后达到的高[Ca2+]i水平会降低。在单细胞水平上,这表现为对谷氨酸产生[Ca2+]i大幅升高反应的神经元数量减少。结果表明,防止[Ca2+]i大幅增加的能力可能是丙酮酸和苹果酸在谷氨酸兴奋性毒性期间发挥有益作用的基础。

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