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强心苷哇巴因可增强成年大鼠海马神经元的兴奋性毒性损伤。

The cardiac glycoside ouabain potentiates excitotoxic injury of adult neurons in rat hippocampus.

作者信息

Brines M L, Dare A O, de Lanerolle N C

机构信息

Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.

出版信息

Neurosci Lett. 1995 May 26;191(3):145-8. doi: 10.1016/0304-3940(95)11577-j.

Abstract

We demonstrate that the enzyme family responsible for the restoration of the transmembrane cation balance, namely the sodium pump (Na+, K(+)-ATPase), plays a critical role in whether glutamate injures adult neurons in vivo. Partial inhibition of the sodium pump by the cardiac glycoside ouabain in young adult rats is not itself damaging. This treatment, however, markedly potentiates ordinarily subtoxic dosages of the glutamate analog kainic acid to produce limbic seizures and widespread neurodegeneration within the hippocampus in a pattern closely resembling that observed for human temporal lobe epilepsy.

摘要

我们证明,负责恢复跨膜阳离子平衡的酶家族,即钠泵(Na⁺,K⁺ - ATP酶),在谷氨酸是否会在体内损伤成年神经元方面起着关键作用。在成年幼鼠中,强心苷哇巴因对钠泵的部分抑制作用本身并无损害。然而,这种处理显著增强了通常亚毒性剂量的谷氨酸类似物 kainic 酸的作用,从而引发边缘叶癫痫发作,并在海马体内造成广泛的神经退行性变,其模式与人类颞叶癫痫中观察到的情况极为相似。

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