• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

In vitro acetylcholine release from rat caudate nucleus as a new model for testing drugs with dopamine-receptor activity.

作者信息

Stoof J C, Thieme R E, Vrijmoed-de Vries M C, Mulder A H

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1979 Nov;309(2):119-24. doi: 10.1007/BF00501218.

DOI:10.1007/BF00501218
PMID:522898
Abstract
摘要

相似文献

1
In vitro acetylcholine release from rat caudate nucleus as a new model for testing drugs with dopamine-receptor activity.大鼠尾状核体外乙酰胆碱释放作为一种测试具有多巴胺受体活性药物的新模型。
Naunyn Schmiedebergs Arch Pharmacol. 1979 Nov;309(2):119-24. doi: 10.1007/BF00501218.
2
Stereoisomers of apomorphine differ in affinity and intrinsic activity at presynaptic dopamine receptors modulating [3H]dopamine and [3H]acetylcholine release in slices of cat caudate.阿扑吗啡的立体异构体对调节猫尾状核切片中[3H]多巴胺和[3H]乙酰胆碱释放的突触前多巴胺受体的亲和力和内在活性不同。
Eur J Pharmacol. 1983 Mar 18;88(1):81-8. doi: 10.1016/0014-2999(83)90394-1.
3
Rapid desensitization of presynaptic dopamine autoreceptors during exposure to exogenous dopamine.暴露于外源性多巴胺期间突触前多巴胺自身受体的快速脱敏
Brain Res. 1985 Jun 24;337(1):11-7. doi: 10.1016/0006-8993(85)91605-1.
4
Somatostatin and cholecystokinin octapeptide differentially modulate the release of [3H]acetylcholine from caudate nucleus but not cerebral cortex: role of dopamine receptor activation.生长抑素和八肽胆囊收缩素对尾状核而非大脑皮质释放[3H]乙酰胆碱有不同的调节作用：多巴胺受体激活的作用。
Brain Res. 1986 May 21;374(1):153-61. doi: 10.1016/0006-8993(86)90404-x.
5
Inhibitory effect of dopamine on acetylcholine release from caudate nucleus.多巴胺对尾状核乙酰胆碱释放的抑制作用。
Pol J Pharmacol Pharm. 1977 May-Jun;29(3):201-11.
6
Chemical lesion and drug induced supersensitivity and subsensitivity of caudate dopamine receptors.化学损伤以及药物诱导的尾状核多巴胺受体超敏反应和低敏反应。
Life Sci. 1978 Aug 7;23(5):443-6. doi: 10.1016/0024-3205(78)90150-9.
7
The contrasting actions of TRH and cycloheximide in altering the effects of centrally acting drugs: evidence for the non-involvement of dopamine sensitive adenylate cyclase.促甲状腺激素释放激素（TRH）与环己酰亚胺在改变中枢作用药物效应方面的相反作用：多巴胺敏感腺苷酸环化酶未参与的证据
Neuropharmacology. 1976 Oct;15(10):591-9. doi: 10.1016/0028-3908(76)90014-9.
8
Essential fatty acids modulate apomorphine activity at dopamine receptors in cat caudate slices.必需脂肪酸调节阿扑吗啡在猫尾状核切片中多巴胺受体上的活性。
Eur J Pharmacol. 1988 May 10;149(3):317-22. doi: 10.1016/0014-2999(88)90662-0.
9
Stimulation of D2-dopamine receptors in rat neostriatum inhibits the release of acetylcholine and dopamine but does not affect the release of gamma-aminobutyric acid, glutamate or serotonin.刺激大鼠新纹状体中的D2 - 多巴胺受体可抑制乙酰胆碱和多巴胺的释放，但不影响γ-氨基丁酸、谷氨酸或5-羟色胺的释放。
Eur J Pharmacol. 1982 Oct 22;84(3-4):211-4. doi: 10.1016/0014-2999(82)90204-7.
10
Effect of psychoytopic drugs on high affinity choline uptake by excised tissue of rat nucleus caudatus.精神药物对大鼠尾状核离体组织高亲和力胆碱摄取的影响。
Brain Res. 1980 Jan 27;182(2):478-81. doi: 10.1016/0006-8993(80)91208-1.

引用本文的文献

1
SDZ GLC 756, a novel octahydrobenzo[g]quinoline derivative exerts opposing effects on dopamine D1 and D2 receptors.SDZ GLC 756，一种新型八氢苯并[g]喹啉衍生物，对多巴胺D1和D2受体具有相反的作用。
J Neural Transm (Vienna). 1996;103(1-2):17-30. doi: 10.1007/BF01292613.
2
SDZ PSD 958, a novel D1 receptor antagonist with potential limbic selectivity.SDZ PSD 958，一种具有潜在边缘系统选择性的新型D1受体拮抗剂。
J Neural Transm (Vienna). 1996;103(3):261-76. doi: 10.1007/BF01271238.
3
Modulation by endogenous dopamine of the release of acetylcholine in the caudate nucleus of the rabbit.

本文引用的文献

1
A rapid, simplified procedure for simultaneous assay of norepinephrine, dopamine, and 5-hydroxytryptamine from discrete brain areas.一种从离散脑区同时测定去甲肾上腺素、多巴胺和5-羟色胺的快速、简化方法。
Anal Biochem. 1971 Feb;39(2):356-72. doi: 10.1016/0003-2697(71)90426-x.
2
Demonstration of acetylcholine release by measuring efflux of labelled choline from cerebral cortical slices.通过测量标记胆碱从大脑皮质切片中的流出量来证明乙酰胆碱的释放。
J Neurochem. 1972 Nov;19(11):2667-77. doi: 10.1111/j.1471-4159.1972.tb01326.x.
3
Release of acetylcholine from hippocampal slices by potassium depolarization: dependence on high affinity choline uptake.
内源性多巴胺对兔尾状核中乙酰胆碱释放的调节作用。
Naunyn Schmiedebergs Arch Pharmacol. 1980;315(2):111-7. doi: 10.1007/BF00499253.
4
Differential anatomical location of [3H]-N,n-propylnorapomorphine and [3H]-spiperone binding sites in the striatum and substantia nigra of the rat.大鼠纹状体和黑质中[3H]-N，N-丙基去甲阿朴吗啡和[3H]-螺哌隆结合位点的差异解剖位置。
Br J Pharmacol. 1983 Jun;79(2):599-610. doi: 10.1111/j.1476-5381.1983.tb11035.x.
5
In vitro effect of the racemic mixture and the (-)enantiomer of N-n-propyl-3-(3-hydroxyphenyl)-piperidine (3-PPP) on postsynaptic dopamine receptors and on a presynaptic dopamine autoreceptor.消旋混合物及N-正丙基-3-(3-羟基苯基)-哌啶（3-PPP）的(-)对映体对突触后多巴胺受体及突触前多巴胺自身受体的体外作用
J Neural Transm. 1983;58(1-2):43-53. doi: 10.1007/BF01249123.
6
Neurochemical effects of some ergot derivatives: a basis for their antiparkinson actions.某些麦角衍生物的神经化学效应：其抗帕金森作用的基础。
J Neural Transm. 1981;51(1-2):39-59. doi: 10.1007/BF01664004.
7
Acetylcholine release in rat nucleus accumbens is regulated through dopamine D2-receptors.大鼠伏隔核中的乙酰胆碱释放通过多巴胺D2受体进行调节。
Naunyn Schmiedebergs Arch Pharmacol. 1988 Sep;338(3):250-5. doi: 10.1007/BF00173396.
8
[3H]205-501, a non-catechol dopaminergic agonist, labels selectively and with high affinity dopamine D2 receptors.[3H]205 - 501，一种非儿茶酚胺多巴胺能激动剂，能选择性且高亲和力地标记多巴胺D2受体。
J Neural Transm. 1985;62(3-4):231-48. doi: 10.1007/BF01252239.
9
Release of acetylcholine and its dopaminergic control in slices from striatal grafts in the ibotenic acid-lesioned rat striatum.鹅膏蕈氨酸损伤大鼠纹状体内纹状体移植片乙酰胆碱的释放及其多巴胺能调控
Naunyn Schmiedebergs Arch Pharmacol. 1988 Dec;338(6):623-31. doi: 10.1007/BF00165626.
10
Intrastriatal dopaminergic grafts restore inhibitory control over striatal cholinergic neurons.纹状体内多巴胺能移植恢复对纹状体胆碱能神经元的抑制性控制。
Exp Brain Res. 1988;73(2):236-48. doi: 10.1007/BF00248216.
钾离子去极化诱导海马切片释放乙酰胆碱：对高亲和力胆碱摄取的依赖性。
Brain Res. 1974 Apr 19;70(2):372-6. doi: 10.1016/0006-8993(74)90329-1.
4
Origin and modulation of acetylcholine activity in the neostriatum.新纹状体中乙酰胆碱活性的起源与调节
Brain Res. 1974 May 10;71(1):167-71. doi: 10.1016/0006-8993(74)90202-9.
5
Evidence on the cellular localization of adenyl cyclase in the neostriatum.新纹状体中腺苷酸环化酶细胞定位的证据。
Brain Res. 1976 Dec 17;118(2):356-8. doi: 10.1016/0006-8993(76)90726-5.
6
Properties of [3H]haloperidol and [3H]dopamine binding associated with dopamine receptors in calf brain membranes.小牛脑膜中与多巴胺受体相关的[3H]氟哌啶醇和[3H]多巴胺结合特性
Mol Pharmacol. 1976 Sep;12(5):800-12.
7
The effect of cholinergic drugs on [3H]acetylcholine release from slices of rat hippocampus, striatum and cortex.胆碱能药物对大鼠海马体、纹状体和皮质切片中[3H]乙酰胆碱释放的影响。
Brain Res. 1977 Mar 11;123(2):311-22. doi: 10.1016/0006-8993(77)90482-6.
8
The effect of bromocriptine on rat striatal adenylate cyclase and rat brain monoamine metabolism.溴隐亭对大鼠纹状体腺苷酸环化酶及大鼠脑单胺代谢的影响。
J Neurochem. 1978 Nov;31(5):1163-72. doi: 10.1111/j.1471-4159.1978.tb06240.x.
9
Effects of some derivatives of 2-aminotetralin on dopamine-sensitive adenylate cyclase and on the binding of (3H)haloperidol to neuroleptic receptors in the rat striatum.2-氨基四氢萘的某些衍生物对大鼠纹状体中多巴胺敏感性腺苷酸环化酶以及（3H）氟哌啶醇与抗精神病药物受体结合的影响。
Biochem Pharmacol. 1978 May 15;27(10):1417-20. doi: 10.1016/0006-2952(78)90094-1.
10
Cerebral dopamine agonist properties of some 2-aminotetralin derivatives after peripheral and intracerebral administration.外周和脑内给药后一些2-氨基四氢萘衍生物的脑多巴胺激动剂特性
J Med Chem. 1977 Sep;20(9):1111-6. doi: 10.1021/jm00219a001.