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The relationship between desensitization and the metaphilic effect at cholinergic receptors.

作者信息

Rang H P, Ritter J M

出版信息

Mol Pharmacol. 1970 Jul;6(4):383-90.

PMID:5429281
Abstract
摘要

相似文献

1
The relationship between desensitization and the metaphilic effect at cholinergic receptors.脱敏作用与胆碱能受体处的亲代谢效应之间的关系。
Mol Pharmacol. 1970 Jul;6(4):383-90.
2
[Responses of under- and extra-synaptical membranes of muscular fibers to acetylcholine and carbachol].
J Physiol (Paris). 1969;61 Suppl 2:289.
3
[Blocking of the neuromuscular conduction by decamethylene-bis-pyridinium].[十亚甲基双吡啶对神经肌肉传导的阻滞作用]
Farmakol Toksikol. 1970 Sep-Oct;33(5):536-8.
4
Succinylcholine and decamethonium: comparison of depolarization and desensitization.琥珀酰胆碱与十烃季铵:去极化与脱敏作用的比较。
Anesthesiology. 1970 Dec;33(6):611-8. doi: 10.1097/00000542-197012000-00007.
5
Affinity of curare-like compounds and their potency in blocking neuromuscular transmission.箭毒样化合物的亲和力及其阻断神经肌肉传递的效能。
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6
Cholinergic activities of halogeno-acetylcholines.卤代乙酰胆碱的胆碱能活性。
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7
On the mechanism of desensitization at cholinergic receptors.关于胆碱能受体脱敏的机制
Mol Pharmacol. 1970 Jul;6(4):357-82.
8
The effects of succinylcholine, decamethonium, hexacarbacholine, gallamine and dimethyl tubocurarine on the twitch and tonic neuromuscular systems of the cat.琥珀酰胆碱、十烃季铵、己氨胆碱、加拉明和二甲基筒箭毒碱对猫的抽搐和强直性神经肌肉系统的作用。
J Pharmacol Exp Ther. 1966 Nov;154(2):303-9.
9
Cholinergic receptor labelling specific irreversible binding of bromoacetylcholine to cholinergic receptors at neuromuscular junctions.胆碱能受体标记:溴乙酰胆碱与神经肌肉接头处胆碱能受体的特异性不可逆结合。
Eur J Pharmacol. 1974 May;26(2):268-76. doi: 10.1016/0014-2999(74)90237-4.
10
Effects of 2-PAM and TMB-4 on neuromuscular transmission.2-解磷定和4-甲基-2-硫代吗啉代丁酸对神经肌肉传递的影响。
J Pharmacol Exp Ther. 1965 Sep;149(3):311-9.

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Differential Activation and Desensitization States Promoted by Noncanonical 7 Nicotinic Acetylcholine Receptor Agonists.非经典 7 型烟碱型乙酰胆碱受体激动剂诱导的激活和脱敏状态的差异。
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2
Fourth gaddum memorial lecture, school of pharmacy, university of london, january 1973.第四届加德姆纪念讲座,伦敦大学药学院,1973年1月
Br J Pharmacol. 1973 Jul;48(3):475-95. doi: 10.1111/j.1476-5381.1973.tb08355.x.
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Use-dependent inhibition of P2X3 receptors by nanomolar agonist.
纳摩尔浓度激动剂对P2X3受体的使用依赖性抑制
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J Neurosci. 2005 Jun 8;25(23):5563-72. doi: 10.1523/JNEUROSCI.5240-04.2005.
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Two-component desensitization of nicotinic receptors induced by acetylcholine agonists in Lymnaea stagnalis neurones.椎实螺神经元中乙酰胆碱激动剂诱导的烟碱样受体双组分脱敏作用
J Physiol. 1984 Aug;353:375-91. doi: 10.1113/jphysiol.1984.sp015341.
6
Changes in neuromuscular junction endplate current time constants produced by sulfhydryl reagents.巯基试剂引起的神经肌肉接头终板电流时间常数的变化
Proc Natl Acad Sci U S A. 1981 Dec;78(12):7806-9. doi: 10.1073/pnas.78.12.7806.
7
Quinacrine (mepacrine) action at frog end-plate.喹吖因(米帕林)对蛙终板的作用。
J Physiol. 1980 Sep;306:261-81. doi: 10.1113/jphysiol.1980.sp013396.
8
The effects of different recording conditions on the estimates of affinity constants of antagonists for acetylcholine receptors in the guinea-pig ileum.不同记录条件对豚鼠回肠中乙酰胆碱受体拮抗剂亲和常数估计值的影响。
Br J Pharmacol. 1972 Oct;46(2):312-4.
9
A transient state concept of drug receptor interaction.
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10
Action of nicotine on identified cells of the snail brain.尼古丁对蜗牛脑部特定细胞的作用。
Naunyn Schmiedebergs Arch Pharmacol. 1973;280(3):275-94. doi: 10.1007/BF00501352.