• 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

固定诱导的纹状体神经元对右旋苯丙胺反应的变化。

Immobilization-induced changes in the response of striatal neurons to dexamphetamine.

作者信息

Warenycia M W, McKenzie G M

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 1983;7(4-6):761-4. doi: 10.1016/0278-5846(83)90061-1.

DOI:10.1016/0278-5846(83)90061-1
PMID:6320305
Abstract

Bipolar multiple unit recording electrodes were implanted in the striata of male Long-Evans rats 5-7 days prior to experimentation. In subsequent experiments, striatal neuronal activity in response to dexamphetamine (1.0 or 2.5 mg/kg i.p.) was recorded in either freely moving or immobilized, artificially-respired rats. Whereas dexamphetamine produced only excitation of striatal neurons in freely moving animals, a multiplicity of responses, ranging from excitation to inhibition, and including biphasic as well as no change responses were observed in immobilized animals. It is concluded that the absence of dexamphetamine-induced behavior in immobilized animals modifies the striatal neuronal response to dexamphetamine, possibly through alteration of the activity of excitatory striatal afferents.

摘要

在实验前5 - 7天,将双极多单元记录电极植入雄性Long-Evans大鼠的纹状体中。在随后的实验中,在自由活动或固定、人工呼吸的大鼠中记录纹状体神经元对右旋苯丙胺(1.0或2.5mg/kg腹腔注射)的反应。虽然右旋苯丙胺在自由活动的动物中仅引起纹状体神经元兴奋,但在固定的动物中观察到多种反应,从兴奋到抑制,包括双相反应以及无变化反应。得出的结论是,固定动物中缺乏右旋苯丙胺诱导的行为改变了纹状体神经元对右旋苯丙胺的反应,可能是通过改变兴奋性纹状体传入神经的活动来实现的。

相似文献

1
Immobilization-induced changes in the response of striatal neurons to dexamphetamine.固定诱导的纹状体神经元对右旋苯丙胺反应的变化。
Prog Neuropsychopharmacol Biol Psychiatry. 1983;7(4-6):761-4. doi: 10.1016/0278-5846(83)90061-1.
2
Immobilization of rats modifies the response of striatal neurons to dexamphetamine.大鼠制动会改变纹状体神经元对右旋苯丙胺的反应。
Pharmacol Biochem Behav. 1984 Jul;21(1):53-9. doi: 10.1016/0091-3057(84)90130-8.
3
The role of afferents from the parafascicular-centromedian complex in the excitatory striatal neuronal response to dexamphetamine in freely moving animals.束旁-中央中复合体传入纤维在自由活动动物中对右旋苯丙胺的纹状体神经元兴奋性反应中的作用。
Prog Neuropsychopharmacol Biol Psychiatry. 1984;8(4-6):757-60. doi: 10.1016/0278-5846(84)90053-8.
4
Pharmacological activity profiles of dopamine D-1 and D-2 reception agonists and antagonists on striatal neuronal activity and the response to dexamphetamine in freely moving rats.多巴胺D-1和D-2受体激动剂与拮抗剂对自由活动大鼠纹状体神经元活动及对右旋苯丙胺反应的药理活性谱
Gen Pharmacol. 1989;20(3):295-301. doi: 10.1016/0306-3623(89)90262-0.
5
Activation of striatal neurons by dexamphetamine is antagonized by degeneration of striatal dopaminergic terminals.
J Neural Transm. 1987;70(3-4):217-32. doi: 10.1007/BF01253599.
6
Decreases in behavioral and striatal neuronal responses to dexamphetamine with aging.随着年龄增长,对右旋苯丙胺的行为和纹状体神经元反应会降低。
Pharmacol Biochem Behav. 1989 Jun;33(2):489-91. doi: 10.1016/0091-3057(89)90536-4.
7
Dexamphetamine increases striatal neuronal firing in freely moving rats.右旋苯丙胺可增加自由活动大鼠纹状体神经元的放电。
Neuropharmacology. 1979 Jun;18(6):547-52. doi: 10.1016/0028-3908(79)90099-6.
8
Simultaneous electrochemical and unit recording measurements: characterization of the effects of D-amphetamine and ascorbic acid on neostriatal neurons.同步电化学与单位记录测量:D-苯丙胺和抗坏血酸对新纹状体神经元影响的特征分析
Brain Res. 1983 Feb 14;261(1):101-8. doi: 10.1016/0006-8993(83)91288-x.
9
The effects of cortical ablation on multiple unit activity in the striatum following dexamphetamine.去氧麻黄碱后皮质切除对纹状体多单位活动的影响。
Neuropharmacology. 1987 Aug;26(8):1107-14. doi: 10.1016/0028-3908(87)90255-3.
10
Bilateral ablation of the corticostriatal projection: behavioral, biochemical and electrophysiological correlates.双侧皮质纹状体投射损毁:行为、生化及电生理相关性
Prog Neuropsychopharmacol Biol Psychiatry. 1984;8(4-6):761-4. doi: 10.1016/0278-5846(84)90054-x.