• 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

部分D2样多巴胺受体激动剂特古瑞得在多巴胺能张力高低状态下均表现为功能性拮抗剂:来自断奶前大鼠的证据。

The partial D2-like dopamine receptor agonist terguride acts as a functional antagonist in states of high and low dopaminergic tone: evidence from preweanling rats.

作者信息

McDougall Sanders A, Hernandez Rita M, Reichel Carmela M, Farley Cristal M

机构信息

Department of Psychology, California State University, San Bernardino, CA, 92407, USA.

出版信息

Psychopharmacology (Berl). 2005 Apr;178(4):431-9. doi: 10.1007/s00213-004-2033-1. Epub 2004 Nov 18.

DOI:10.1007/s00213-004-2033-1
PMID:15765258
Abstract

RATIONALE

In adult rats, the partial D(2)-like agonist terguride acts as an antagonist at normosensitive D(2)-like post-synaptic receptors, while it acts as an agonist at the same receptors during states of low dopaminergic tone.

OBJECTIVE

The purpose of the present study was to determine whether partial D(2)-like agonists exhibit both antagonistic and agonistic actions during the preweanling period.

METHODS

In experiments 1 and 2 (examining the agonistic actions of terguride), preweanling rats were either given an escalating regimen of amphetamine to induce a state of amphetamine withdrawal or pretreated with the tyrosine hydroxylase inhibitor AMPT. Distance traveled was measured after rats were injected with saline, terguride (0.4-1.6 mg/kg), or the full D(2)-like receptor agonist NPA (0.01 mg/kg). In experiment 3 (examining the antagonistic actions of terguride), preweanling rats were pretreated with terguride 30 min before they were tested with saline, NPA (0.05 mg/kg), or amphetamine (1.5 mg/kg).

RESULTS

NPA had an exaggerated locomotor activating effect when tested under conditions of amphetamine withdrawal, while the partial D(2)-like agonist did not enhance distance traveled under any circumstance. Similarly, NPA increased and terguride did not affect the distance-traveled scores of AMPT-pretreated rats. In experiment 3, terguride pretreatment significantly reduced the distance traveled of amphetamine-treated and NPA-treated rats.

CONCLUSIONS

The behavioral evidence indicates that, during the preweanling period, terguride antagonizes D(2)-like post-synaptic receptors in a state of high dopaminergic tone; however, there is no evidence that terguride is capable of stimulating D(2)-like post-synaptic receptors during states of low dopaminergic tone.

摘要

理论依据

在成年大鼠中,部分D₂样激动剂特古瑞得在正常敏感的D₂样突触后受体上起拮抗剂作用,而在多巴胺能张力较低的状态下,它在相同受体上起激动剂作用。

目的

本研究的目的是确定部分D₂样激动剂在断奶前阶段是否表现出拮抗和激动作用。

方法

在实验1和实验2(研究特古瑞得的激动作用)中,给断奶前的大鼠给予递增剂量的苯丙胺以诱导苯丙胺戒断状态,或用酪氨酸羟化酶抑制剂AMPT进行预处理。在大鼠注射生理盐水、特古瑞得(0.4 - 1.6毫克/千克)或完全D₂样受体激动剂NPA(0.01毫克/千克)后,测量其行进距离。在实验3(研究特古瑞得的拮抗作用)中,在断奶前的大鼠用生理盐水、NPA(0.05毫克/千克)或苯丙胺(1.5毫克/千克)进行测试前30分钟,用特古瑞得进行预处理。

结果

在苯丙胺戒断条件下进行测试时,NPA具有夸大的运动激活作用,而部分D₂样激动剂在任何情况下都不会增加行进距离。同样,NPA增加了AMPT预处理大鼠的行进距离得分,而特古瑞得没有影响。在实验3中,特古瑞得预处理显著降低了苯丙胺处理和NPA处理大鼠的行进距离。

结论

行为学证据表明,在断奶前阶段,特古瑞得在多巴胺能张力高的状态下拮抗D₂样突触后受体;然而,没有证据表明特古瑞得在多巴胺能张力低的状态下能够刺激D₂样突触后受体。

相似文献

1
The partial D2-like dopamine receptor agonist terguride acts as a functional antagonist in states of high and low dopaminergic tone: evidence from preweanling rats.部分D2样多巴胺受体激动剂特古瑞得在多巴胺能张力高低状态下均表现为功能性拮抗剂:来自断奶前大鼠的证据。
Psychopharmacology (Berl). 2005 Apr;178(4):431-9. doi: 10.1007/s00213-004-2033-1. Epub 2004 Nov 18.
2
The partial dopamine D2-like receptor agonist terguride functions as an agonist in preweanling rats after a 5-day reserpine regimen.在进行5天利血平治疗方案后,部分多巴胺D2样受体激动剂替古瑞定在断奶前大鼠中发挥激动剂作用。
Psychopharmacology (Berl). 2006 Mar;185(1):104-11. doi: 10.1007/s00213-005-0263-5. Epub 2006 Jan 31.
3
Effects of a partial D2-like receptor agonist on striatal dopamine autoreceptor functioning in preweanling rats.部分D2样受体激动剂对断奶前大鼠纹状体多巴胺自身受体功能的影响。
Brain Res. 2006 Feb 16;1073-1074:269-75. doi: 10.1016/j.brainres.2005.12.054. Epub 2006 Jan 19.
4
Effects of a partial dopamine D2-like agonist on the cocaine-induced behavioral sensitization of preweanling rats.部分多巴胺D2样激动剂对可卡因诱导的断奶前大鼠行为敏化的影响。
Pharmacol Biochem Behav. 2003 Aug;76(1):27-34. doi: 10.1016/s0091-3057(03)00188-6.
5
Pre- and postsynaptic actions of a partial D2 receptor agonist in reserpinized young rats: longevity of agonistic effects.利血平化幼鼠中部分D2受体激动剂的突触前和突触后作用:激动效应的持续时间
Brain Res. 2006 Dec 8;1124(1):37-44. doi: 10.1016/j.brainres.2006.09.068. Epub 2006 Oct 27.
6
Behavioral effects of dopamine receptor inactivation in the caudate-putamen of preweanling rats: role of the D2 receptor.幼鼠纹状体腹侧被盖区多巴胺受体失活的行为效应:D2 受体的作用。
Psychopharmacology (Berl). 2014 Feb;231(4):651-62. doi: 10.1007/s00213-013-3280-9. Epub 2013 Sep 22.
7
Suppression of cocaine- and food-maintained behavior by the D2-like receptor partial agonist terguride in squirrel monkeys.D2样受体部分激动剂terguride对松鼠猴可卡因及食物维持行为的抑制作用
Psychopharmacology (Berl). 2003 Mar;166(3):298-305. doi: 10.1007/s00213-002-1347-0. Epub 2003 Feb 13.
8
Effects of aripiprazole and terguride on dopamine synthesis in the dorsal striatum and medial prefrontal cortex of preweanling rats.阿立哌唑和替古瑞肽对断奶前大鼠背侧纹状体和内侧前额叶皮质多巴胺合成的影响。
J Neural Transm (Vienna). 2008;115(1):97-106. doi: 10.1007/s00702-007-0820-7. Epub 2007 Nov 12.
9
The dopamine D(2) partial agonist and antagonist terguride decreases heroin self-administration on fixed- and progressive-ratio schedules.多巴胺 D(2)部分激动剂和拮抗剂曲格列酮降低了固定比例和递增比例条件下的海洛因自我给药。
Pharmacol Biochem Behav. 2010 Dec;97(2):222-6. doi: 10.1016/j.pbb.2010.08.002. Epub 2010 Aug 10.
10
A dopamine partial agonist and antagonist block amphetamine self-administration in a progressive ratio schedule.多巴胺部分激动剂和拮抗剂以渐进比率程序阻断苯丙胺自我给药。
Pharmacol Biochem Behav. 2001 Apr;68(4):701-8. doi: 10.1016/s0091-3057(01)00472-5.

引用本文的文献

1
Intraamygdaloid Oxytocin Increases Time Spent on Social Interaction in Valproate-Induced Autism Animal Model.杏仁核内催产素增加丙戊酸盐诱导的自闭症动物模型中社交互动的时间。
Biomedicines. 2023 Jun 23;11(7):1802. doi: 10.3390/biomedicines11071802.
2
Effects of dopamine and serotonin synthesis inhibitors on the ketamine-, d-amphetamine-, and cocaine-induced locomotor activity of preweanling and adolescent rats: sex differences.多巴胺和 5-羟色胺合成抑制剂对新生和青春期大鼠氯胺酮、安非他命和可卡因诱导的运动活动的影响:性别差异。
Behav Brain Res. 2020 Feb 3;379:112302. doi: 10.1016/j.bbr.2019.112302. Epub 2019 Oct 23.
3
Development of a peptide targeting dopamine transporter to improve ADHD-like deficits.

本文引用的文献

1
Effects of a partial dopamine D2-like agonist on the cocaine-induced behavioral sensitization of preweanling rats.部分多巴胺D2样激动剂对可卡因诱导的断奶前大鼠行为敏化的影响。
Pharmacol Biochem Behav. 2003 Aug;76(1):27-34. doi: 10.1016/s0091-3057(03)00188-6.
2
Ontogenesis of behavioral sensitization and conditioned place preference induced by psychostimulants in laboratory rodents.实验室啮齿动物中精神兴奋剂诱导的行为敏化和条件性位置偏爱(偏好)的个体发生。
Neurosci Biobehav Rev. 2003 Jan-Mar;27(1-2):163-78. doi: 10.1016/s0149-7634(03)00018-6.
3
Differential actions of antiparkinson agents at multiple classes of monoaminergic receptor. II. Agonist and antagonist properties at subtypes of dopamine D(2)-like receptor and alpha(1)/alpha(2)-adrenoceptor.
开发一种靶向多巴胺转运体的肽以改善 ADHD 样缺陷。
Mol Brain. 2018 Nov 9;11(1):66. doi: 10.1186/s13041-018-0409-0.
4
Ontogenetic differences in sensitivity to LiCl- and amphetamine-induced taste avoidance in preweanling rats.在新生期大鼠中,锂盐和安非他命诱导的味觉回避的敏感性存在个体发育差异。
Chem Senses. 2011 Jul;36(6):565-77. doi: 10.1093/chemse/bjr026. Epub 2011 Mar 28.
5
The partial dopamine D2-like receptor agonist terguride functions as an agonist in preweanling rats after a 5-day reserpine regimen.在进行5天利血平治疗方案后,部分多巴胺D2样受体激动剂替古瑞定在断奶前大鼠中发挥激动剂作用。
Psychopharmacology (Berl). 2006 Mar;185(1):104-11. doi: 10.1007/s00213-005-0263-5. Epub 2006 Jan 31.
抗帕金森药物对多类单胺能受体的不同作用。II. 对多巴胺D(2)样受体和α(1)/α(2) -肾上腺素能受体亚型的激动剂和拮抗剂特性。
J Pharmacol Exp Ther. 2002 Nov;303(2):805-14. doi: 10.1124/jpet.102.039875.
4
Aripiprazole, a novel antipsychotic, is a high-affinity partial agonist at human dopamine D2 receptors.阿立哌唑是一种新型抗精神病药物,对人多巴胺D2受体具有高亲和力的部分激动剂。
J Pharmacol Exp Ther. 2002 Jul;302(1):381-9. doi: 10.1124/jpet.102.033175.
5
Dopamine partial agonist reverses amphetamine withdrawal in rats.多巴胺部分激动剂可逆转大鼠的苯丙胺戒断症状。
Neuropsychopharmacology. 2001 Nov;25(5):789-92. doi: 10.1016/S0893-133X(01)00270-6.
6
Reinforcing effects of D2 dopamine receptor agonists and partial agonists in rhesus monkeys.
Drug Alcohol Depend. 2001 Oct 1;64(2):209-17. doi: 10.1016/s0376-8716(01)00124-7.
7
A dopamine partial agonist and antagonist block amphetamine self-administration in a progressive ratio schedule.多巴胺部分激动剂和拮抗剂以渐进比率程序阻断苯丙胺自我给药。
Pharmacol Biochem Behav. 2001 Apr;68(4):701-8. doi: 10.1016/s0091-3057(01)00472-5.
8
Inhibitory effects of partial D2 dopamine receptor agonists on the d-amphetamine discriminative cue.
Behav Pharmacol. 1989;1(2):101-111.
9
Withdrawal following repeated exposure to d-amphetamine decreases responding for a sucrose solution as measured by a progressive ratio schedule of reinforcement.通过渐进性比率强化程序测量,反复接触右旋苯丙胺后的戒断会降低对蔗糖溶液的反应。
Psychopharmacology (Berl). 1999 Jan;141(1):99-106. doi: 10.1007/s002130050812.
10
Characterization of the effects of the partial dopamine agonist terguride on cocaine self-administration in the rat.部分多巴胺激动剂替古瑞肽对大鼠可卡因自我给药影响的特征分析。
J Pharmacol Exp Ther. 1998 Sep;286(3):1231-8.