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Stereospecific in vitro binding of [3H]dexetimide to brain muscarinic receptors.

作者信息

Laduron P M, Verwimp M, Leysen J E

出版信息

J Neurochem. 1979 Feb;32(2):421-7. doi: 10.1111/j.1471-4159.1979.tb00366.x.

DOI:10.1111/j.1471-4159.1979.tb00366.x
PMID:762557
Abstract
摘要

相似文献

1
Stereospecific in vitro binding of [3H]dexetimide to brain muscarinic receptors.
J Neurochem. 1979 Feb;32(2):421-7. doi: 10.1111/j.1471-4159.1979.tb00366.x.
2
Characterization and subcellular localization of brain muscarinic receptors labelled in vivo by [3H]dexetimide.用[3H]右旋苯乙哌啶体内标记的脑毒蕈碱受体的表征及亚细胞定位
J Neurochem. 1979 Dec;33(6):1223-31. doi: 10.1111/j.1471-4159.1979.tb05268.x.
3
Inhibition of [3H]dexetimide binding by a homologous series of methylfurthrethonium analogues at the peripheral muscarinic receptor.一系列甲基呋索氯铵类似物在外周毒蕈碱受体上对[3H]右旋苯乙呱啶结合的抑制作用。
Biochem Biophys Res Commun. 1980 Nov 28;97(2):430-6. doi: 10.1016/0006-291x(80)90282-x.
4
Axonal flow of muscarinic receptors.毒蕈碱受体的轴浆运输
Arch Int Pharmacodyn Ther. 1980 Apr;244(2):338-40.
5
'Do abnormalities in agonist receptor-binding reflect the activation of the receptor?' An interpretation of the inhibition of 3H-dexetimide binding to the muscarinic receptor by a series of furtrethonium derivatives.
Eur J Respir Dis Suppl. 1984;135:161-3.
6
Biochemical studies on muscarinic receptors.
Biomedicine. 1977 Jul;26(4):250-9.
7
[3H]-Quinuclidinyl benzilate binding to muscarinic receptors in rat brain: comparison of results from intact brain slices and homogenates.[3H]-东莨菪碱与大鼠脑内毒蕈碱受体的结合：完整脑片与匀浆结果的比较
Br J Pharmacol. 1979 Mar;65(3):451-6. doi: 10.1111/j.1476-5381.1979.tb07850.x.
8
Regional heterogeneity of muscarinic receptors of mouse brain.
FEBS Lett. 1979 Jan 15;97(2):265-8. doi: 10.1016/0014-5793(79)80099-x.
9
The binding of antagonists to brain muscarinic receptors.拮抗剂与脑内毒蕈碱受体的结合。
Mol Pharmacol. 1978 Sep;14(5):737-50.
10
Properties and distribution of muscarinic cholinergic receptors in rat striatal micropunched tissue homogenates.大鼠纹状体微穿孔组织匀浆中毒蕈碱型胆碱能受体的特性与分布
Eur J Pharmacol. 1981 Apr 9;70(4):559-64. doi: 10.1016/0014-2999(81)90367-8.

引用本文的文献

1
Risperidone compared with new and reference antipsychotic drugs: in vitro and in vivo receptor binding.利培酮与新型及参比抗精神病药物的比较：体外和体内受体结合情况
Psychopharmacology (Berl). 1996 Mar;124(1-2):57-73. doi: 10.1007/BF02245606.
2
Central effects of paraoxon on haemodynamics in the cat.对氧磷对猫血流动力学的中枢效应。
Naunyn Schmiedebergs Arch Pharmacol. 1981 Sep;317(2):168-72. doi: 10.1007/BF00500075.
3
The effects of paraoxon on blood pressure in the anaesthetized and in the conscious rat.对氧磷对麻醉大鼠和清醒大鼠血压的影响。
Br J Pharmacol. 1982 Oct;77(2):223-32. doi: 10.1111/j.1476-5381.1982.tb09289.x.
4
Purification of muscarinic acetylcholine receptors by affinity chromatography.通过亲和色谱法纯化毒蕈碱型乙酰胆碱受体。
EMBO J. 1983;2(4):499-504. doi: 10.1002/j.1460-2075.1983.tb01453.x.
5
Neurochemical effects of minaprine, a novel psychotropic drug, on the central cholinergic system of the rat.新型精神药物米那普明对大鼠中枢胆碱能系统的神经化学作用。
Psychopharmacology (Berl). 1984;82(3):210-4. doi: 10.1007/BF00427775.
6
Monoclonal antibodies against the native or denatured forms of muscarinic acetylcholine receptors.针对毒蕈碱型乙酰胆碱受体天然或变性形式的单克隆抗体。
EMBO J. 1984 Jan;3(1):17-21. doi: 10.1002/j.1460-2075.1984.tb01755.x.
7
Monoclonal antibodies to purified muscarinic receptor display agonist-like activity.针对纯化的毒蕈碱受体的单克隆抗体表现出类似激动剂的活性。
Proc Natl Acad Sci U S A. 1984 Jul;81(14):4331-4. doi: 10.1073/pnas.81.14.4331.