毒蕈碱型乙酰胆碱受体相互作用：激动剂和拮抗剂的竞争结合研究 - Suppr

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超能文献

Muscarinic acetylcholine receptors interactions: competition binding studies with agonists and antagonists.

作者信息

Kloog Y, Sokolovsky M

出版信息

Brain Res. 1977 Sep 23;134(1):167-72. doi: 10.1016/0006-8993(77)90936-2.

DOI:10.1016/0006-8993(77)90936-2

PMID:912416

Abstract

摘要

相似文献

Muscarinic acetylcholine receptors interactions: competition binding studies with agonists and antagonists.毒蕈碱型乙酰胆碱受体相互作用：激动剂和拮抗剂的竞争结合研究

Brain Res. 1977 Sep 23;134(1):167-72. doi: 10.1016/0006-8993(77)90936-2.

Effects of oxotremorine demonstrate presynaptic muscarinic and dopaminergic receptors on motor nerve terminals.氧化震颤素对运动神经末梢的作用表明存在突触前毒蕈碱能和多巴胺能受体。

Nature. 1979 Apr 12;278(5705):645-6. doi: 10.1038/278645a0.

Oxotremorine-tolerance: muscarinic blockade or homeostatic adaptation?氧化震颤素耐受性：毒蕈碱阻断还是稳态适应？

Acta Physiol Acad Sci Hung. 1979;53(1):55-9.

Muscarinic activity of some secondary and tertiary amines and quaternary ammonium salts structurally related to oxotremorine.一些与氧化震颤素结构相关的仲胺、叔胺和季铵盐的毒蕈碱活性。

Eur J Pharmacol. 1983 Mar 4;87(4):387-96. doi: 10.1016/0014-2999(83)90077-8.

In vivo regulation of muscarinic cholinergic receptors in embryonic chick brain.胚胎鸡脑内毒蕈碱型胆碱能受体的体内调节

Mol Pharmacol. 1982 Mar;21(2):280-6.

Muscarinic receptor subsensitivity in the longitudinal muscle of the rat ileum following chronic anticholinesterase treatment with diisopropylfluorophosphate.用二异丙基氟磷酸进行慢性抗胆碱酯酶治疗后大鼠回肠纵肌中的毒蕈碱受体敏感性降低。

Biochem Pharmacol. 1980 May 15;29(10):1391-7. doi: 10.1016/0006-2952(80)90435-9.

Types of muscarinic response in Xenopus oocytes.非洲爪蟾卵母细胞中的毒蕈碱反应类型。

Life Sci. 1980 Oct 13;27(15):1423-8. doi: 10.1016/0024-3205(80)90407-5.

N-Ethylmaleimide-induced alteration in the interaction of agonists with muscarinic cholinergic receptors of rat brain.

J Pharmacol Exp Ther. 1983 Jan;224(1):118-26.

Relative affinities of drugs acting at cholinoceptors in displacing agonist and antagonist radioligands: the NMS/Oxo-M ratio as an index of efficacy at cortical muscarinic receptors.作用于胆碱能受体的药物在置换激动剂和拮抗剂放射性配体方面的相对亲和力：NMS/Oxo-M 比值作为皮质毒蕈碱受体效能的指标。

Br J Pharmacol. 1988 Feb;93(2):437-45. doi: 10.1111/j.1476-5381.1988.tb11451.x.

Pharmacological evidence of muscarinic-cholinergic sensitization following chronic stress.

Psychopharmacology (Berl). 2001 May;155(2):144-7. doi: 10.1007/s002130100690.

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Prediction of protein-ligand binding affinity via deep learning models.通过深度学习模型预测蛋白质-配体结合亲和力。

Brief Bioinform. 2024 Jan 22;25(2). doi: 10.1093/bib/bbae081.

The interaction of amine local anaesthetics with muscarinic receptors.胺类局部麻醉药与毒蕈碱受体的相互作用。

Br J Pharmacol. 1980;71(1):327-35. doi: 10.1111/j.1476-5381.1980.tb10943.x.

Regional distribution of the muscarinic cholinoceptor and acetylcholinesterase in guinea pig brain.豚鼠脑内毒蕈碱型胆碱能受体和乙酰胆碱酯酶的区域分布

Neurochem Res. 1980 Aug;5(8):809-15. doi: 10.1007/BF00965781.

Aging and rat brain muscarinic receptors as measured by quinuclidinyl benzilate binding.通过奎宁环基苯甲酸酯结合法测定衰老与大鼠脑毒蕈碱受体

Neurochem Res. 1980 Mar;5(3):301-8. doi: 10.1007/BF00964618.

Binding of [3H]-pilocarpine to membranes from rat cerebral cortex.[3H]-毛果芸香碱与大鼠大脑皮质膜的结合

Naunyn Schmiedebergs Arch Pharmacol. 1981 Sep;317(2):126-30. doi: 10.1007/BF00500067.

Actions of various muscarinic agonists on membrane potential, potassium efflux, and contraction of longitudinal muscle of guinea-pig intestine.各种毒蕈碱激动剂对豚鼠肠纵肌膜电位、钾外流和收缩的作用。

Br J Pharmacol. 1981 Feb;72(2):319-34. doi: 10.1111/j.1476-5381.1981.tb09131.x.

Molecular regulation of receptors: interaction of beta-estradiol and progesterone with the muscarinic system.受体的分子调控：β-雌二醇和孕酮与毒蕈碱系统的相互作用

Proc Natl Acad Sci U S A. 1981 Sep;78(9):5554-8. doi: 10.1073/pnas.78.9.5554.

Two ligands may bind simultaneously to the muscarine receptor.两种配体可能同时与毒蕈碱受体结合。

Naunyn Schmiedebergs Arch Pharmacol. 1982 Jul;320(1):3-13. doi: 10.1007/BF00499064.

Muscarinic cholinergic receptor binding in rat mast cells.大鼠肥大细胞中的毒蕈碱型胆碱能受体结合

Agents Actions. 1983 Jun;13(4):327-32. doi: 10.1007/BF01971484.

Enthalpy-entropy relationship in drug-cholinoceptor interaction: a new approach.药物与胆碱能受体相互作用中的焓-熵关系：一种新方法。

Br J Pharmacol. 1985 Aug;85(4):889-96. doi: 10.1111/j.1476-5381.1985.tb11088.x.

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