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Anatoxin-a a potent ligand for nicotinic cholinergic receptors in rat brain.

作者信息

Zhang X, Stjernlöf P, Adem A, Nordberg A

出版信息

Eur J Pharmacol. 1987 Mar 31;135(3):457-8. doi: 10.1016/0014-2999(87)90702-3.

DOI:10.1016/0014-2999(87)90702-3
PMID:3582504
Abstract
摘要

相似文献

1
Anatoxin-a a potent ligand for nicotinic cholinergic receptors in rat brain.
Eur J Pharmacol. 1987 Mar 31;135(3):457-8. doi: 10.1016/0014-2999(87)90702-3.
2
Anatoxin-a: a novel, potent agonist at the nicotinic receptor.类毒素-a：一种新型的、对烟碱样受体有强效作用的激动剂。
Mol Pharmacol. 1980 Nov;18(3):384-94.
3
Anatoxin-a interactions with cholinergic synaptic molecules.类毒素-a与胆碱能突触分子的相互作用。
Proc Natl Acad Sci U S A. 1981 Jul;78(7):4639-43. doi: 10.1073/pnas.78.7.4639.
4
N-methylation of anatoxin-a abolishes nicotinic cholinergic activity.
Toxicon. 1990;28(2):133-4. doi: 10.1016/0041-0101(90)90331-z.
5
(+)-Anatoxin-a is a potent agonist at neuronal nicotinic acetylcholine receptors.（+）-anatoxin-a是神经元烟碱型乙酰胆碱受体的强效激动剂。
J Neurochem. 1993 Jun;60(6):2308-11. doi: 10.1111/j.1471-4159.1993.tb03519.x.
6
N-methylanatoxinol isomers: derivatives of the agonist (+)-anatoxin-a block the nicotinic acetylcholine receptor ion channel.
Mol Pharmacol. 1989 Feb;35(2):223-31.
7
Methyllycaconitine and (+)-anatoxin-a differentiate between nicotinic receptors in vertebrate and invertebrate nervous systems.甲基lycaconitine和（+）-anatoxin-a可区分脊椎动物和无脊椎动物神经系统中的烟碱受体。
FEBS Lett. 1988 Jan 4;226(2):357-63. doi: 10.1016/0014-5793(88)81454-6.
8
Molecular mechanisms of the potent and stereospecific nicotinic receptor agonist (+)-anatoxin-a.强效立体特异性烟碱受体激动剂（+）-anatoxin-a的分子机制
Mol Pharmacol. 1986 Mar;29(3):250-7.
9
Behavioural effects of anatoxin, a potent nicotinic agonist, in rats.
Neuropharmacology. 1992 Mar;31(3):311-4. doi: 10.1016/0028-3908(92)90182-o.
10
Activation and blockade of the acetylcholine receptor-ion channel by the agonists (+)-anatoxin-a, the N-methyl derivative and the enantiomer.
J Pharmacol Exp Ther. 1990 Feb;252(2):517-25.

引用本文的文献

1
Assessment of the Effects of Anatoxin-a In Vitro: Cytotoxicity and Uptake.体外评估类毒素-a的作用：细胞毒性和摄取
Toxins (Basel). 2024 Dec 13;16(12):541. doi: 10.3390/toxins16120541.
2
Toxic Effects Produced by Anatoxin-a under Laboratory Conditions: A Review.实验室条件下生成的anatoxin-a 的毒性作用：综述。
Toxins (Basel). 2022 Dec 8;14(12):861. doi: 10.3390/toxins14120861.
3
In vivo neurochemical characterization of anatoxin-a evoked dopamine release from striatum.河鲀毒素诱发纹状体多巴胺释放的体内神经化学特征
J Neural Transm (Vienna). 2007 Feb;114(2):173-84. doi: 10.1007/s00702-006-0542-2. Epub 2006 Aug 8.
4
An improved nicotinic pharmacophore and a stereoselective CoMFA-model for nicotinic agonists acting at the central nicotinic acetylcholine receptors labelled by.
J Comput Aided Mol Des. 2001 Mar;15(3):247-58. doi: 10.1023/a:1008140021426.
5
The competition of (-)-[3H]nicotine binding by the enantiomers of nicotine, nornicotine and anatoxin-a in membranes and solubilized preparations of different brain regions of rat.
Naunyn Schmiedebergs Arch Pharmacol. 1993 Jul;348(1):28-34. doi: 10.1007/BF00168533.
6
Do tetrahydroaminoacridine (THA) and physostigmine restore acetylcholine release in Alzheimer brains via nicotinic receptors?
J Neural Transm. 1987;70(3-4):357-68. doi: 10.1007/BF01253610.
7
Molecular studies of the neuronal nicotinic acetylcholine receptor family.神经元烟碱型乙酰胆碱受体家族的分子研究
Mol Neurobiol. 1987 Winter;1(4):281-337. doi: 10.1007/BF02935740.
8
Effect of acute and subchronic nicotine treatment on cortical acetylcholine release and on nicotinic receptors in rats and guinea-pigs.急性和亚慢性尼古丁处理对大鼠和豚鼠皮质乙酰胆碱释放及烟碱型受体的影响。
Br J Pharmacol. 1989 Sep;98(1):71-8. doi: 10.1111/j.1476-5381.1989.tb16864.x.
9
A comparison of the binding of nicotine and nornicotine stereoisomers to nicotinic binding sites in rat brain cortex.大鼠脑皮质中尼古丁和去甲烟碱立体异构体与烟碱结合位点结合情况的比较。
Naunyn Schmiedebergs Arch Pharmacol. 1991 Feb;343(2):123-7. doi: 10.1007/BF00168598.