Bradaïa A, Trouslard J
Laboratoire de Neurophysiologie Cellulaire et Intégrée, UMR 7519 CNRS/ULP, 21 rue R. Descartes, 67084 Strasbourg Cedex, France.
J Physiol. 2002 Nov 1;544(3):727-39. doi: 10.1113/jphysiol.2002.028894.
Using patch clamp recordings on neonatal rat spinal cord slices, we have looked for the presence of alpha-bungarotoxin-sensitive nicotinic ACh receptors (nAChRs) on sympathetic preganglionic neurones (SPNs) surrounding the central canal of the spinal cord (lamina X) and examined whether they were implicated in a fast cholinergic synaptic transmission. SPNs were identified either by their morphology using biocytin in the recording electrode and/or by antidromic stimulation of the ventral rootlets. The selective alpha7-containing nAChR (alpha7nAChR) agonist choline (10 mM) induced a fast, rapidly desensitizing inward current, which was fully blocked by alpha-bungarotoxin (alpha-BgT; 50 nM) and strychnine (1 microM), two antagonists of alpha7nAChRs. The I-V relationship of the choline-induced current showed a strong inward-going rectification. Electrically evoked excitatory postsynaptic currents (eEPSCs) could be recorded. At -60 mV, eEPSCs peaked at -26.2 pA and decayed monoexponentially with a mean time constant of 8.5 ms. The current-voltage relationship for eEPSCs exhibited a strong inward rectification and a reversal potential close to 0 mV, compatible with a non-selective cationic current. The appearance of eEPSCs was entirely suppressed by the application of 100 microM ACh or nicotine. Choline (10 mM) and 1,1-dimethyl-4-phenylpiperazinium iodide (DMPP; 100 microM) both reduced the amplitude of eEPSCs, whereas cytisine (100 microM) had no effect. Strychnine (1 microM) and alpha-BgT (50 nM) both suppressed the eEPSCs. Blocking the P2X purinergic and 5-HT(3) receptors had no effect on eEPSCs. DMPP induced four types of current, which differed in their onset and desensitization rate. The most frequently encountered responses were insensitive to the action of strychnine and alpha-BgT, and were reproduced by ACh and nicotine but not by cytisine. We conclude that SPNs of the lamina X express several classes of nAChRs and in particular alpha-BgT-sensitive nAChRs. This is the first demonstration in a mammalian spinal cord preparation of a fast cholinergic neurotransmission in which alpha-BgT-sensitive nicotinic receptors are involved.
利用新生大鼠脊髓切片的膜片钳记录技术,我们探寻了脊髓中央管(X层)周围交感神经节前神经元(SPN)上是否存在α-银环蛇毒素敏感的烟碱型乙酰胆碱受体(nAChR),并研究了它们是否参与快速胆碱能突触传递。通过在记录电极中使用生物胞素观察其形态和/或通过对腹侧神经根进行逆向刺激来识别SPN。选择性含α7的nAChR(α7nAChR)激动剂胆碱(10 mM)诱导出一种快速、迅速脱敏的内向电流,该电流被α7nAChR的两种拮抗剂α-银环蛇毒素(α-BgT;50 nM)和士的宁(1 μM)完全阻断。胆碱诱导电流的I-V关系显示出强烈的内向整流。可以记录电诱发的兴奋性突触后电流(eEPSC)。在-60 mV时,eEPSC峰值为-26.2 pA,并以单指数形式衰减,平均时间常数为8.5 ms。eEPSC的电流-电压关系表现出强烈的内向整流,反转电位接近0 mV,与非选择性阳离子电流一致。应用100 μM乙酰胆碱或尼古丁可完全抑制eEPSC的出现。胆碱(10 mM)和1,1-二甲基-4-苯基哌嗪碘化物(DMPP;100 μM)均降低了eEPSC的幅度,而金雀花碱(100 μM)则无作用。士的宁(1 μM)和α-BgT(50 nM)均抑制了eEPSC。阻断P2X嘌呤能受体和5-HT(3)受体对eEPSC无影响。DMPP诱导出四种类型的电流,它们在起始和脱敏速率上有所不同。最常见的反应对士的宁和α-BgT的作用不敏感,可被乙酰胆碱和尼古丁重现,但不能被金雀花碱重现。我们得出结论,X层的SPN表达多种类型的nAChR,尤其是α-BgT敏感的nAChR。这是在哺乳动物脊髓制备中首次证明涉及α-BgT敏感烟碱型受体的快速胆碱能神经传递。