Developmental regulation of T-, N- and L-type calcium currents in mouse embryonic sensory neurones

被引:20
作者
Desmadryl, G
Hilaire, C
Vigues, S
Diochot, S
Valmier, J
机构
[1] Inst Biol, CNRS, ERS 155, F-34060 Montpellier, France
[2] INSERM, U432, F-34095 Montpellier 5, France
关键词
dihydropyridines; omega-conotoxin GVIA; LVA barium current; HVA barium current; DRG neurones;
D O I
10.1046/j.1460-9568.1998.00055.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated the development of a low (T-type) and two high voltage-activated (N- and L-type) calcium channel currents in large diameter dorsal root ganglion neurones acutely isolated from embryonic mice using the whole-cell patch-clamp technique. The low and high voltage-activated barium currents (LVA and HVA) were identified by their distinct threshold of activation and their sensitivity to pharmacological agents, dihydropyridines and omega-conotoxin-GVIA, at embryonic day 13(E13), E15 and E17-18, respectively, before, during and after synaptogenesis. The amplitude and density of LVA currents, measured during a -40 mV pulse from a holding potential of -100 mV, increased significantly between E13 and E15, and remained constant between E15 and E17-18, The density of global HVA current, elicited by O mV pulse, increased between E13 and E15/E17-18. The density of the N-type current studied by the application of omega-conotoxin-GVIA (1 mu M) increased significantly between E13 and E15/E17-18. The use of the dihydropyridine nitrendipine (1 mu M) revealed that the density of L-type current remained constant at each stage of development. Nevertheless, application of dihydropyridine Bay K 8644 (3 mu M) demonstrated a significant slowing of the deactivation tail current between embryonic days 13 and 15, which may reflect a qualitative maturation of this Class of calcium channel current, The temporal relationship between the changes in calcium channel pattern and the period of target innervation suggests possible roles of T-, N- and L-type currents during developmental key events such as natural neurone death and onset of synapse formation.
引用
收藏
页码:545 / 552
页数:8
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