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培养的大鼠小脑颗粒神经元中钙离子通道电流的特性分析

Characterization of Ca2+ channel currents in cultured rat cerebellar granule neurones.

作者信息

Pearson H A, Sutton K G, Scott R H, Dolphin A C

机构信息

Department of Pharmacology, Royal Free Hospital School of Medicine, London, UK.

出版信息

J Physiol. 1995 Feb 1;482 ( Pt 3)(Pt 3):493-509. doi: 10.1113/jphysiol.1995.sp020535.

Abstract
  1. High-threshold voltage-gated calcium channel currents (IBa) were studied in cultured rat cerebellar granule neurones using the whole-cell patch clamp technique with 10 mM Ba2+ as the charge carrier. The putative P-type component of whole-cell current was characterized by utilizing the toxin omega-agatoxin IVA (omega-Aga IVA) in combination with other blockers. 2. omega-Aga IVA (100 nM) inhibited the high voltage-activated (HVA) IBa by 40.9 +/- 3.4% (n = 27), and the dissociation constant Kd was 2.7 nM. Maximal inhibition occurred within a 2-3 min time course, and was irreversible. The isolated omega-Aga IVA-sensitive current was non-inactivating. 3. omega-Aga IVA exhibited overlapping selectivity with both N- and L-channel blockers; omega-conotoxin GVIA (omega-CTX GVIA) (1 microM) and the dihydropyridine (-)-202-709 (1 microM), respectively. Together these toxins reduced the omega-Aga IVA-sensitive component to just 4.5 +/- 1.4% (n = 3). Thus only a small proportion of the current can be unequivocally attributed to P-type current. Inhibition of the HVA IBa by omega-Aga IA also reduced the proportion of omega-Aga IVA-sensitive current to 28.0 +/- 3.2% (n = 3). 4. Application of omega-Aga IVA and a synthetic form of funnel-web toxin, N-(7-amino-4-azaheptyl)-L-argininamide (sFTX-3.3; 10 microM), produced an additive block of the HVA IBa. Consequently these two toxins do not act on the same channel in cerebellar granule neurones. 5. omega-Aga IVA inhibition of low voltage-activated (LVA) IBa was studied in the ND7-23 neuronal cell line. omega-Aga IVA (100 nM) reduced the LVA current by 41.3 +/- 3.2% (n = 17) in a fully reversible manner with no shift in the steady-state inactivation of the channel. 6. A component of current insensitive to N-, L- and P-channel blockers remained unclassified in all our studies. This component, and also that remaining following block by omega-Aga IVA and omega-Aga IA, exhibited relatively rapid, although incomplete, inactivation compared to the other currents isolated in this study. 7. In conclusion, omega-Aga IVA inhibits a component of current in cultured cerebellar granule neurones which overlaps almost completely with that inhibited by L- and N-channel blockers. In addition, a large component of whole-cell current in these neurones still remains unclassified.
摘要
  1. 采用全细胞膜片钳技术,以10 mM Ba2+作为载流子,研究了培养的大鼠小脑颗粒神经元中的高阈值电压门控钙通道电流(IBa)。利用毒素ω-芋螺毒素IVA(ω-Aga IVA)与其他阻滞剂相结合,对全细胞电流的假定P型成分进行了表征。2. ω-Aga IVA(100 nM)使高电压激活(HVA)的IBa抑制了40.9±3.4%(n = 27),解离常数Kd为2.7 nM。最大抑制在2 - 3分钟内出现,且不可逆。分离出的ω-Aga IVA敏感电流不发生失活。3. ω-Aga IVA与N型和L型通道阻滞剂表现出重叠的选择性;分别为ω-芋螺毒素GVIA(ω-CTX GVIA)(1 μM)和二氢吡啶(-)-202 - 709(1 μM)。这些毒素共同作用使ω-Aga IVA敏感成分仅降至4.5±1.4%(n = 3)。因此,只有一小部分电流可明确归因于P型电流。ω-Aga IA对HVA IBa的抑制也使ω-Aga IVA敏感电流的比例降至28.0±3.2%(n = 3)。4. 应用ω-Aga IVA和一种合成形式的漏斗网毒素N-(7-氨基-4-氮杂庚基)-L-精氨酰胺(sFTX-3.3;10 μM)对HVA IBa产生了相加性阻断。因此,这两种毒素在小脑颗粒神经元中作用于不同的通道。5. 在ND7-23神经元细胞系中研究了ω-Aga IVA对低电压激活(LVA)IBa的抑制作用。ω-Aga IVA(100 nM)以完全可逆的方式使LVA电流降低了41.3±3.2%(n = 17),且通道的稳态失活无偏移。6. 在我们所有的研究中,对N型、L型和P型通道阻滞剂不敏感的电流成分仍未分类。与本研究中分离出的其他电流相比,该成分以及在被ω-Aga IVA和ω-Aga IA阻断后剩余的成分表现出相对快速但不完全的失活。7. 总之,ω-Aga IVA抑制培养的小脑颗粒神经元中的一部分电流,该电流几乎与被L型和N型通道阻滞剂抑制的电流完全重叠。此外,这些神经元中全细胞电流的很大一部分仍未分类。

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