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介导大鼠听觉脑干突触传递的钙通道类型的发育变化

Developmental changes in calcium channel types mediating synaptic transmission in rat auditory brainstem.

作者信息

Iwasaki S, Takahashi T

机构信息

Department of Neurophysiology, University of Tokyo Faculty of Medicine, Tokyo 113-0033, Japan.

出版信息

J Physiol. 1998 Jun 1;509 ( Pt 2)(Pt 2):419-23. doi: 10.1111/j.1469-7793.1998.419bn.x.

Abstract
  1. Calcium channel blockers were tested on excitatory postsynaptic currents (EPSCs) at the synapse formed by the calyx of Held on the principal cells in the medial nucleus of trapezoid body (MNTB) in brainstem slices of 4- to 14-day-old rats. 2. At postnatal day 4-9 (P4-9), EPSCs were irreversibly suppressed by the P/Q-type Ca2+ channel blocker omega-agatoxin-IVA (omega-Aga-IVA, 200 nM) and also by the N-type Ca2+ channel blocker omega-conotoxin GVIA (omega-CgTx, 2 microM). A small fraction of EPSCs was resistant to both toxins but abolished by Cd2+ (100 microM). 3. After P7, the omega-CgTx-sensitive EPSC fraction diminished and eventually disappeared after P10. Concomitantly the fraction insensitive to both toxins decreased and became undetectable after P10. 4. In contrast, the omega-Aga-IVA-sensitive EPSC fraction increased with development and became predominant after P10. All through the developmental period examined, the L-type Ca2+ channel blocker nicardipine (10 microM) had no effect. 5. We conclude that presynaptic Ca2+ channel types triggering transmitter release undergo developmental switching during the early postnatal period.
摘要
  1. 在4至14日龄大鼠脑干切片中,对由Held壶腹与梯形体内侧核(MNTB)主细胞形成的突触处的兴奋性突触后电流(EPSC)进行了钙通道阻滞剂测试。2. 在出生后第4至9天(P4 - 9),EPSC被P/Q型钙通道阻滞剂ω - 芋螺毒素IVA(ω - Aga - IVA,200 nM)以及N型钙通道阻滞剂ω - 芋螺毒素GVIA(ω - CgTx,2 μM)不可逆地抑制。一小部分EPSC对两种毒素均有抗性,但可被Cd2 +(100 μM)消除。3. P7之后,ω - CgTx敏感的EPSC部分减少,并在P10之后最终消失。与此同时,对两种毒素均不敏感的部分减少,并在P10之后变得无法检测到。4. 相反,ω - Aga - IVA敏感的EPSC部分随着发育增加,并在P10之后占主导地位。在所研究的整个发育时期,L型钙通道阻滞剂尼卡地平(1 μM)没有作用。5. 我们得出结论,在出生后早期,触发递质释放的突触前钙通道类型会发生发育性转换。

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