The permeation and activation properties of brain sodium channels change during development

被引:5
作者
Castillo, C
Thomhill, WB
Zhu, J
Recio-Pinto, E
机构
[1] Inst Estudios Avanzados, Caracas 1015 A, Venezuela
[2] Fordham Univ, Dept Biol Sci, Bronx, NY 10458 USA
[3] NYU, Sch Med, Dept Anesthesiol, New York, NY 10016 USA
来源
DEVELOPMENTAL BRAIN RESEARCH | 2003年 / 144卷 / 01期
关键词
voltage-dependent sodium channel; sialylation; glycosylation; channel function during development; rat forebrain;
D O I
10.1016/S0165-3806(03)00164-0
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
BTX-modified sodium channels from 15-day embryonic (E15) rat forebrains were studied in planar lipid bilayers. Compared to postnatal sodium channels. E15 channels had a lower maximal single channel conductance, whereas their permeation pathway sensed a comparable surface charge density and had a similar apparent binding affinity for sodium ions. The steady-state activation curve of E15 channels was significantly more hyperpolarized and had a shallower slope than postnatal channels. The apparent BTX binding affinity was significantly lower for E15 channels than for postnatal channels. Finally, E15 channel alpha-subunits displayed a lower apparent molecular weight. and a lower sialylation level than postnatal sodium channel alpha-subunits. Together with previous studies, our data suggested that the observed functional differences between E15 and postnatal voltage-dependent sodium channels cannot be explained solely by the observed differences in channel sialylation, and hence they also appeared to reflect the presence of other channel structural differences. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:99 / 106
页数:8
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