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Catechol, a facilitatory drug that demonstrates only a prejunctional site of action.

作者信息

Gallagher J P, Blaber L C

出版信息

J Pharmacol Exp Ther. 1973 Jan;184(1):129-35.

PMID:4686002
Abstract
摘要

相似文献

1
Catechol, a facilitatory drug that demonstrates only a prejunctional site of action.儿茶酚,一种仅显示节前作用位点的促进性药物。
J Pharmacol Exp Ther. 1973 Jan;184(1):129-35.
2
The facilitatory effects of catechol and phenol at the neuromuscular junction of the cat.儿茶酚和苯酚对猫神经肌肉接头的促进作用。
Neuropharmacology. 1971 Mar;10(21):153-9. doi: 10.1016/0028-3908(71)90036-0.
3
Mechanisms of dual action of nicotine on end-plate membranes.尼古丁对终板膜双重作用的机制。
J Pharmacol Exp Ther. 1972 Sep;182(3):427-41.
4
The effect of facilitatory concentrations of decamethonium on the storage and release of transmitter at the neuromuscular junction of the cat.十烃季铵的促进浓度对猫神经肌肉接头处递质储存和释放的影响。
J Pharmacol Exp Ther. 1970 Dec;175(3):664-72.
5
[Calcium current of nerve ending in the frog].[青蛙神经末梢的钙电流]
Dokl Akad Nauk SSSR. 1985;282(3):744-6.
6
Prejunctional and postjunctional cholinoceptors at the neuromuscular junction.神经肌肉接头处的接头前和接头后胆碱能受体。
Anesth Analg. 1980 Dec;59(12):935-43.
7
The action of tubocurarine at the neuromuscular junction [proceedings].筒箭毒碱在神经肌肉接头处的作用[会议论文集]
J Physiol. 1978 Nov;284:171P-172P.
8
Facilitatory sites of action of theophylline in isolated cat tenuissimus muscle.氨茶碱在离体猫薄肌中的易化作用位点。
Neuropharmacology. 1973 Sep;12(9):885-95. doi: 10.1016/0028-3908(73)90041-5.
9
Competitive block and ion channel block as mechanisms of antagonist action on the skeletal muscle end-plate.竞争性阻断和离子通道阻断作为拮抗剂作用于骨骼肌终板的机制。
Adv Biochem Psychopharmacol. 1980;21:67-80.
10
[Comparative sensitivity of neuro-muscular synapses of different muscles toward d-tubocurarine chloride and alpha-truxillic acid].
Farmakol Toksikol. 1967 Mar-Apr;30(2):152-6.

引用本文的文献

1
Nicotinic antagonist-produced frequency-dependent changes in acetylcholine release from rat motor nerve terminals.烟碱拮抗剂对大鼠运动神经末梢乙酰胆碱释放产生频率依赖性变化。
J Physiol. 1994 May 1;476(3):517-29. doi: 10.1113/jphysiol.1994.sp020151.
2
Microelectrode recording of the effects of agonists and antagonists on alpha-adrenoceptors on rat somatic nerve terminals.微电极记录激动剂和拮抗剂对大鼠躯体神经末梢α-肾上腺素能受体的作用。
Br J Pharmacol. 1983 Sep;80(1):41-6. doi: 10.1111/j.1476-5381.1983.tb11047.x.
3
The effect of the convulsant agent, catechol, on neurotransmitter uptake and release in rat brain slices.
惊厥剂儿茶酚对大鼠脑片神经递质摄取和释放的影响。
Br J Pharmacol. 1981 Nov;74(3):715-21. doi: 10.1111/j.1476-5381.1981.tb10483.x.
4
Some characteristics of the long-latency component of the evoked muscle response induced by administration of catechol to the anaesthetized rat: a neurophysiological and neuropharmacological investigation.对麻醉大鼠注射儿茶酚胺所诱发的肌肉反应的长潜伏期成分的一些特征:一项神经生理学和神经药理学研究。
Br J Pharmacol. 1984 Sep;83(1):83-8. doi: 10.1111/j.1476-5381.1984.tb10122.x.
5
Effects of the facilitatory compounds catechol, guanidine, noradrenaline and phencyclidine on presynaptic currents of mouse motor nerve terminals.易化性化合物儿茶酚、胍、去甲肾上腺素和苯环利定对小鼠运动神经末梢突触前电流的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1988 Aug;338(2):133-7. doi: 10.1007/BF00174860.
6
Non involvement of gamma-aminobutyric acid in catechol-induced seizures.γ-氨基丁酸不参与儿茶酚胺诱发的癫痫发作。
Br J Pharmacol. 1986 Jan;87(1):167-73. doi: 10.1111/j.1476-5381.1986.tb10168.x.
7
Sites and mechanisms of action of catechol (1,2-dihydroxybenzene) in the rat olfactory cortex slice.儿茶酚(1,2 - 二羟基苯)在大鼠嗅觉皮质切片中的作用位点及作用机制。
Br J Pharmacol. 1986 Jun;88(2):433-40. doi: 10.1111/j.1476-5381.1986.tb10221.x.
8
Catechol: a potent and specific inhibitor of the fast potassium channel in frog primary afferent neurones.儿茶酚:青蛙初级传入神经元快速钾通道的一种强效特异性抑制剂。
J Physiol. 1986 Apr;373:115-27. doi: 10.1113/jphysiol.1986.sp016038.
9
A pharmacological study of the spontaneous convulsive activity induced by 1,2-dihydroxybenzene (catechol) in the anaesthetized mouse.对麻醉小鼠中由1,2 - 二羟基苯(儿茶酚)诱导的自发惊厥活动的药理学研究。
Br J Pharmacol. 1977 Nov;61(3):433-9. doi: 10.1111/j.1476-5381.1977.tb08437.x.