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Dual effect of calmidazolium (R 24571) on transmitter release at the frog neuromuscular junction.

作者信息

Sahaf Z Y, Publicover S J

出版信息

Brain Res. 1985 Nov 25;348(1):192-6. doi: 10.1016/0006-8993(85)90379-8.

DOI:10.1016/0006-8993(85)90379-8
PMID:2998560
Abstract

The effect of the non-phenothiazine calmodulin-inhibitor R 24571 on transmitter release at the frog neuromuscular junction has been investigated. MEPP frequency was reduced by 25-40% at low concentrations of the drug (2-5 X 10(-7) M) but increased at higher concentrations. These effects were independent of [Ca2+]o. EPP quantal content was increased at low levels of release (quantal content 0.5-1.5) and was unaffected at higher levels (quantal content 30-40). It is concluded that R 24571 has both inhibitory and stimulatory effects, but that evoked release of transmitter is insensitive to the inhibitory action of the drug.

摘要

相似文献

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Dual effect of calmidazolium (R 24571) on transmitter release at the frog neuromuscular junction.
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引用本文的文献

1
Calmodulin increases transmitter release by mobilizing quanta at the frog motor nerve terminal.钙调蛋白通过动员蛙运动神经末梢的量子来增加递质释放。
Br J Pharmacol. 2002 Nov;137(5):719-27. doi: 10.1038/sj.bjp.0704923.
2
Postsynaptic inhibitory effects of phenothiazines at cholinergic synapses may not involve calmodulin.吩噻嗪类药物在胆碱能突触处的突触后抑制作用可能与钙调蛋白无关。
Naunyn Schmiedebergs Arch Pharmacol. 1986 Aug;333(4):454-6. doi: 10.1007/BF00500024.
3
Trifluoperazine-sensitive activation of the spontaneous transmitter release at the frog motor endplates by low doses of procaine.
低剂量普鲁卡因对蛙运动终板自发性递质释放的三氟拉嗪敏感激活作用。
Naunyn Schmiedebergs Arch Pharmacol. 1987 Sep;336(3):257-61. doi: 10.1007/BF00172675.