Suppr超能文献

发育中神经元内钠内流引发的电压依赖性钠通道下调。

Down-regulation of voltage-dependent sodium channels initiated by sodium influx in developing neurons.

作者信息

Dargent B, Couraud F

机构信息

Laboratoire de Biochimie, Centre National de la Recherche Scientifique UA 1179, Faculté de Médecine-Secteur Nord, Marseille, France.

出版信息

Proc Natl Acad Sci U S A. 1990 Aug;87(15):5907-11. doi: 10.1073/pnas.87.15.5907.

Abstract

To address the issue of whether regulatory feedback exists between the electrical activity of a neuron and ion-channel density, we investigated the effect of Na(+)-channel activators (scorpion alpha toxin, batrachotoxin, and veratridine) on the density of Na+ channels in fetal rat brain neurons in vitro. A partial but rapid (t1/2, 15 min) disappearance of surface Na+ channels was observed as measured by a decrease in the specific binding of [3H]saxitoxin and 125I-labeled scorpion beta toxin and a decrease in specific 22Na+ uptake. Moreover, the increase in the number of Na+ channels that normally occurs during neuronal maturation in vitro was inhibited by chronic channel activator treatment. The induced disappearance of Na+ channels was abolished by tetrodotoxin, was found to be dependent on the external Na+ concentration, and was prevented when either choline (a nonpermeant ion) or Li+ (a permeant ion) was substituted for Na+. Amphotericin B, a Na+ ionophore, and monensin were able to mimick the effect of Na(+)-channel activators, while a KCl depolarization failed to do this. This feedback regulation seems to be a neuronal property since Na(+)-channel density in cultured astrocytes was not affected by channel activator treatment or by amphotericin B. The present evidence suggests that an increase in intracellular Na+ concentration, whether elicited by Na(+)-channel activators or mediated by a Na+ ionophore, can induce a decrease in surface Na+ channels and therefore is involved in down-regulation of Na(+)-channel density in fetal rat brain neurons in vitro.

摘要

为了解决神经元电活动与离子通道密度之间是否存在调节反馈的问题,我们研究了Na(+)通道激活剂(蝎毒α毒素、箭毒蛙毒素和藜芦碱)对体外培养的胎鼠脑神经元中Na+通道密度的影响。通过[3H]石房蛤毒素和125I标记的蝎毒β毒素特异性结合的减少以及特异性22Na+摄取的减少来测量,观察到表面Na+通道部分但快速(t1/2,15分钟)消失。此外,慢性通道激活剂处理抑制了体外神经元成熟过程中正常发生的Na+通道数量增加。河豚毒素消除了诱导的Na+通道消失,发现其依赖于细胞外Na+浓度,并且当用胆碱(一种非渗透性离子)或Li+(一种渗透性离子)替代Na+时可防止这种情况。两性霉素B,一种Na+离子载体,和莫能菌素能够模拟Na(+)通道激活剂的作用,而KCl去极化则不能。这种反馈调节似乎是神经元的特性,因为培养的星形胶质细胞中的Na(+)通道密度不受通道激活剂处理或两性霉素B的影响。目前的证据表明,细胞内Na+浓度的增加,无论是由Na(+)通道激活剂引起还是由Na+离子载体介导,都可导致表面Na+通道减少,因此参与体外培养的胎鼠脑神经元中Na(+)通道密度的下调。

相似文献

2
Sodium channel internalization in developing neurons.
Neuron. 1994 Sep;13(3):683-90. doi: 10.1016/0896-6273(94)90035-3.

引用本文的文献

2
Voltage-gated sodium channels in excitable cells as drug targets.可兴奋细胞中的电压门控钠通道作为药物靶点。
Nat Rev Drug Discov. 2025 May;24(5):358-378. doi: 10.1038/s41573-024-01108-x. Epub 2025 Feb 3.
10
Channelopathies: summary of the hot topic keynotes session.通道病:热门话题主旨演讲概要。
Neurotoxicology. 2011 Oct;32(5):661-5. doi: 10.1016/j.neuro.2011.06.002. Epub 2011 Jul 2.

本文引用的文献

10
Functional properties of the subtype of insulin receptor found on neurons.
J Neurochem. 1988 Sep;51(3):878-87. doi: 10.1111/j.1471-4159.1988.tb01824.x.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验