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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Multiple types of calcium channels mediate transmitter release during functional recovery of botulinum toxin type A-poisoned mouse motor nerve terminals.
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Multiple types of calcium channels mediate transmitter release during functional recovery of botulinum toxin type A-poisoned mouse motor nerve terminals.

机译:在肉毒杆菌毒素A型中毒的小鼠运动神经末梢功能恢复期间,多种类型的钙通道介导变送器释放。

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The involvement of different types of voltage-dependent calcium channels in nerve-evoked release of neurotransmitter was studied during recovery from neuromuscular paralysis produced by botulinum toxin type A intoxication. For this purpose, a single subcutaneous injection of botulinum toxin (1 IU; DL50) on to the surface of the mouse levator auris longus muscle was performed. The muscles were removed at several time-points after injection (i.e. at one, two, three, four, five, six and 12 weeks). Using electrophysiological techniques, we studied the effect of different types of calcium channel blockers (nitrendipine, omega-conotoxin-GVIA and omega-agatoxin-IVA) on the quantal content of synaptic transmission elicited by nerve stimulation. Morphological analysis using the conventional silver impregnation technique was also made. During the first four weeks after intoxication, sprouts were found at 80% of motor nerve terminals, while at 12 weeks their number was decreased and the nerve terminals were enlarged. The L-type channel blocker nitrendipine (1 microM) inhibited neurotransmitter release by 80% and 30% at two and five weeks, respectively, while no effects were found at later times. The N-type channel blocker omega-conotoxin-GVIA (1 microM) inhibited neurotransmitter release by 50-70% in muscles studied at two to six weeks, respectively, and had no effect 12 weeks after intoxication. The P-type channel blocker omega-agatoxin-IVA (100 nM) strongly reduced nerve-evoked transmitter release (>90%) at all the time-points studied. Identified motor nerve terminals were also sensitive to both nitrendipine and omega-conotoxin-GVIA. This study shows that multiple voltage-dependent calcium channels were coupled to transmitter release during the period of sprouting and consolidation, suggesting that they may be involved in the nerve ending functional recovery process.
机译:在A型肉毒毒素中毒引起的神经肌肉麻痹恢复过程中,研究了不同类型的电压依赖性钙通道在神经诱发的神经递质释放中的参与。为此目的,在小鼠长耳肌表面上皮下注射了肉毒杆菌毒素(1 IU; DL50)。注射后几个时间点(即一,二,三,四,五,六和十二周)取出肌肉。使用电生理技术,我们研究了不同类型的钙通道阻滞剂(硝苯地平,ω-芋螺毒素-GVIA和ω-藻毒素毒素-IVA)对神经刺激引起的突触传递的定量含量的影响。还使用常规的银浸渍技术进行了形态分析。在中毒后的前四周,在80%的运动神经末梢发现了芽,而在第12周时,芽的数量减少了,神经末梢扩大了。 L型通道阻滞剂尼群地平(1 microM)在两周和五周时分别抑制了80%和30%的神经递质释放,但后来没有发现任何作用。 N型通道阻滞剂ω-芋螺毒素-GVIA(1 microM)分别在两到六周的肌肉中抑制了50-70%的神经递质释放,中毒后12周没有作用。在所有研究的时间点,P型通道阻滞剂欧米伽-毒素(IVA)(100 nM)都大大降低了神经诱发的递质释放(> 90%)。识别出的运动神经末梢对尼群地平和ω-芋螺毒素-GVIA均敏感。这项研究表明,在发芽和巩固期间,多个电压依赖性钙通道与递质释放相关,表明它们可能参与了神经末梢功能恢复过程。

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