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河豚毒素诱导的钙峰:正常和去传入浦肯野细胞的体外和体内研究

Tetrodotoxin induced calcium spikes: in vitro and in vivo studies of normal and deafferented Purkinje cells.

作者信息

Aubry A, Batini C, Billard J M, Kado R T, Morain P

机构信息

Laboratoire de Physiologie de la Motricité, URA 385, CNRS, Université Pierre et Marie Curie, CHU Pitié-Salpétrière, Paris, France.

出版信息

Exp Brain Res. 1991;84(2):297-302. doi: 10.1007/BF00231449.

Abstract

Tetrodotoxin (TTX) is widely used to block the sodium dependent action potential in excitable cells to study their other ionic properties. TTX applied outside, selectively blocks voltage dependent sodium channels and is thought to have no other effects. We report here that TTX, applied to slices of rat cerebellum, suppressed sodium spikes of the Purkinje cells and induced firing in bursts of slower spikes. This activity was blocked by cobalt (2 mM) or cadmium (0.2 mM) in the medium as well as by hyperpolarizing currents showing that the slow spikes were due to voltage dependent calcium channels. The membrane potential was not significantly changed by TTX and the spikes during the bursts had the same threshold potentials and peak spike amplitudes as the voltage and Ca2+ dependent dendritic spikes evoked by injected current before adding TTX. This indicated that no marked changes in the membrane conductances were produced by the TTX. Unlike the burst firing induced by removing extracellular sodium, the TTX induced bursts were not followed by a large hyperpolarization. The same kind of results were obtained with extracellular recording in the in-vivo preparation with TTX applied topically or by pressure near the recording sites. TTX induced burst firing was not due to blocking afferent inhibitory input to the PC, since bicuculline (10(-6) M) applied without TTX, produced only increased firing of fast action potentials and no bursts. The bursts could be arrested within 1 to 2 min by intravenously administering 2 mg/kg sodium pentobarbital, the blockage lasted from 5 to 15 min.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

河豚毒素(TTX)被广泛用于阻断可兴奋细胞中依赖钠的动作电位,以研究其其他离子特性。在细胞外部施加TTX可选择性阻断电压依赖性钠通道,并且一般认为没有其他作用。我们在此报告,将TTX应用于大鼠小脑切片时,可抑制浦肯野细胞的钠峰,并诱导出较慢的峰发放。这种活动在培养基中被钴(2 mM)或镉(0.2 mM)以及超极化电流所阻断,表明慢峰是由电压依赖性钙通道引起的。TTX对膜电位没有显著影响,并且发放期间的峰与添加TTX之前由注入电流诱发的电压和Ca2+依赖性树突峰具有相同的阈值电位和峰峰幅度。这表明TTX没有引起膜电导的明显变化。与去除细胞外钠诱导的爆发性发放不同,TTX诱导的爆发性发放之后没有出现大幅度的超极化。在体内实验中,通过在记录部位附近局部应用或通过压力施加TTX进行细胞外记录,也获得了相同的结果。TTX诱导的爆发性发放不是由于阻断了对浦肯野细胞的传入抑制性输入,因为在没有TTX的情况下应用荷包牡丹碱(10(-6) M),只会增加快速动作电位的发放,而不会产生爆发性发放。静脉注射2 mg/kg戊巴比妥钠可在1至2分钟内使爆发性发放停止,阻断持续5至15分钟。(摘要截短至250字)

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