• 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

多巴胺受体激动剂普拉克索可逆转应激诱导的快感缺失。

Reversal of stress-induced anhedonia by the dopamine receptor agonist, pramipexole.

作者信息

Willner P, Lappas S, Cheeta S, Muscat R

机构信息

Department of Psychology, City of London Polytechnic, UK.

出版信息

Psychopharmacology (Berl). 1994 Aug;115(4):454-62. doi: 10.1007/BF02245568.

DOI:10.1007/BF02245568
PMID:7871089
Abstract

Chronic exposure to mild unpredictable stress has previously been found to depress the consumption of a palatable (1%) sucrose solution, and to attenuate food-induced place preference conditioning. In this study the effects of pramipexole (SND-919), a dopamine D2 agonist, were studied during 7-9 weeks of chronic treatment. Pramipexole (1.0 mg/kg per day) reversed the suppression of sucrose intake in stressed animals, increasing sucrose intakes above the levels seen in untreated nonstressed controls. Pramipexole also increased sucrose intake in nonstressed animals; these effects were accompanied by increases in water intake and tended to correlate with weight loss. Drug-treated stressed animals also lost weight, but in this case water intake was unaffected. A second group of animals received a higher dose of pramipexole (2.0 mg/kg per day). The effects of the two doses were very similar. After three weeks of treatment, these animals were switched to a lower dose of pramipexole (0.1 mg/kg per day). Increases in sucrose intake were maintained over three weeks of treatment at the lower dose, with significant recovery of body weight. Two further groups received the same doses of pramipexole (1.0 mg/kg for 6 weeks or 2.0 mg/kg for 3 weeks followed by 0.1 mg/kg thereafter), but received intermittent (twice-weekly) drug treatment. Intermittent pramipexole treatments also tended to increase sucrose intakes, but the results were less consistent from week to week. Following 6-8 weeks of pramipexole treatment, food-induced place preference conditioning was studied in all animals.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

先前已发现,长期暴露于轻度不可预测应激会降低美味(1%)蔗糖溶液的摄入量,并减弱食物诱导的位置偏爱条件反射。在本研究中,对多巴胺D2激动剂普拉克索(SND - 919)在7 - 9周长期治疗期间的作用进行了研究。普拉克索(每天1.0毫克/千克)逆转了应激动物蔗糖摄入量的抑制,使蔗糖摄入量增加至未处理的非应激对照动物所见水平之上。普拉克索还增加了非应激动物的蔗糖摄入量;这些作用伴随着饮水量增加,且往往与体重减轻相关。药物治疗的应激动物也出现体重减轻,但在这种情况下饮水量未受影响。第二组动物接受更高剂量的普拉克索(每天2.0毫克/千克)。两种剂量的作用非常相似。治疗三周后,这些动物换用较低剂量的普拉克索(每天0.1毫克/千克)。在较低剂量治疗的三周内,蔗糖摄入量持续增加,体重显著恢复。另外两组接受相同剂量的普拉克索(1.0毫克/千克,持续6周或2.0毫克/千克,持续3周,之后为0.1毫克/千克),但接受间歇性(每周两次)药物治疗。间歇性普拉克索治疗也往往会增加蔗糖摄入量,但每周的结果不太一致。在普拉克索治疗6 - 8周后,对所有动物进行了食物诱导的位置偏爱条件反射研究。(摘要截断于250字)

相似文献

1
Reversal of stress-induced anhedonia by the dopamine receptor agonist, pramipexole.多巴胺受体激动剂普拉克索可逆转应激诱导的快感缺失。
Psychopharmacology (Berl). 1994 Aug;115(4):454-62. doi: 10.1007/BF02245568.
2
Behavioural sensitization to a dopamine agonist is associated with reversal of stress-induced anhedonia.对多巴胺激动剂的行为敏化与应激诱导的快感缺失的逆转有关。
Psychopharmacology (Berl). 1993;110(1-2):159-64. doi: 10.1007/BF02246966.
3
Reversal of stress-induced anhedonia by the atypical antidepressants, fluoxetine and maprotiline.非典型抗抑郁药氟西汀和马普替林可逆转应激诱导的快感缺失。
Psychopharmacology (Berl). 1992;109(4):433-8. doi: 10.1007/BF02247719.
4
Anti-anhedonic actions of the novel serotonergic agent flibanserin, a potential rapidly-acting antidepressant.新型5-羟色胺能药物氟立班丝氨的抗快感缺失作用,一种潜在的速效抗抑郁药。
Eur J Pharmacol. 1997 Dec 11;340(2-3):121-32. doi: 10.1016/s0014-2999(97)01412-x.
5
Stereospecific reversal of stress-induced anhedonia by mianserin and its (+)-enantiomer.米安色林及其(+)-对映体对应激诱导的快感缺失的立体特异性逆转。
Psychopharmacology (Berl). 1994 Dec;116(4):523-8. doi: 10.1007/BF02247488.
6
The behavioural effects of pramipexole, a novel dopamine receptor agonist.新型多巴胺受体激动剂普拉克索的行为学效应
Eur J Pharmacol. 1997 Apr 11;324(1):31-7. doi: 10.1016/s0014-2999(97)00066-6.
7
Subsensitivity to rewarding and locomotor stimulant effects of a dopamine agonist following chronic mild stress.慢性轻度应激后对多巴胺激动剂奖赏和运动兴奋作用的敏感性降低
Psychopharmacology (Berl). 1993;110(1-2):152-8. doi: 10.1007/BF02246965.
8
An animal model of anhedonia: attenuation of sucrose consumption and place preference conditioning by chronic unpredictable mild stress.快感缺失的动物模型:慢性不可预测轻度应激对蔗糖消耗及位置偏爱条件反射的减弱作用
Psychopharmacology (Berl). 1991;104(2):255-9. doi: 10.1007/BF02244188.
9
Behavioural evidence that different neurochemical mechanisms underly stretching-yawning and penile erection induced in male rats by SND 919, a new selective D2 dopamine receptor agonist.行为学证据表明,新型选择性D2多巴胺受体激动剂SND 919在雄性大鼠中诱发的伸展打哈欠和阴茎勃起是由不同的神经化学机制介导的。
Psychopharmacology (Berl). 1993;113(2):172-6. doi: 10.1007/BF02245694.
10
Potential antidepressant properties of pramipexole detected in locomotor and operant behavioral investigations in mice.在小鼠的运动和操作性行为研究中检测到普拉克索的潜在抗抑郁特性。
Psychopharmacology (Berl). 2002 Oct;163(3-4):495-500. doi: 10.1007/s00213-002-1199-7. Epub 2002 Aug 29.

引用本文的文献

1
Pramipexole in addition to mood stabilisers for treatment-resistant bipolar depression: the PAX-BD randomised double-blind placebo-controlled trial.普拉克索联合心境稳定剂治疗难治性双相抑郁:PAX - BD随机双盲安慰剂对照试验
Health Technol Assess. 2025 May;29(21):1-216. doi: 10.3310/HBFC1953.
2
A randomised double-blind, placebo-controlled trial of pramipexole in addition to mood stabilisers for patients with treatment-resistant bipolar depression (the PAX-BD study).一项针对难治性双相抑郁症患者的随机双盲、安慰剂对照试验,在使用心境稳定剂的基础上加用普拉克索(PAX-BD研究)。
J Psychopharmacol. 2025 Feb;39(2):106-120. doi: 10.1177/02698811241309622. Epub 2025 Jan 20.
3

本文引用的文献

1
Attenuation of place preference conditioning but not place aversion conditioning by chronic mild stress.慢性轻度应激对条件性位置偏爱形成的抑制作用,但不影响条件性位置厌恶的形成。
J Psychopharmacol. 1992 Jan;6(3):352-6. doi: 10.1177/026988119200600302.
2
Effects of moclobemide, a new generation reversible Mao-A inhibitor, in a novel animal model of depression.新一代可逆性单胺氧化酶A抑制剂吗氯贝胺在新型抑郁症动物模型中的作用。
Pharmacopsychiatry. 1993 Jan;26(1):30-3. doi: 10.1055/s-2007-1014338.
3
Behavioural sensitization to a dopamine agonist is associated with reversal of stress-induced anhedonia.
Effect of Cariprazine on Anhedonia in Patients with Bipolar I Depression: Post Hoc Analysis of Three Randomized Placebo-Controlled Clinical Trials.
卡立普嗪对双相I型抑郁症患者快感缺失的影响:三项随机安慰剂对照临床试验的事后分析
Adv Ther. 2025 Jan;42(1):246-260. doi: 10.1007/s12325-024-03009-2. Epub 2024 Nov 9.
4
Antidepressant- and Anxiolytic-like Effects of Pomegranate: Is It Acting by Common or Well-Known Mechanisms of Action?石榴的抗抑郁和抗焦虑样作用:其作用机制是常见的还是已知的?
Plants (Basel). 2024 Aug 9;13(16):2205. doi: 10.3390/plants13162205.
5
Brain region specific regulation of anandamide (down) and sphingosine-1-phosphate (up) in association with anxiety (AEA) and resilience (S1P) in a mouse model of chronic unpredictable mild stress.慢性不可预测轻度应激小鼠模型中与焦虑(AEA)和韧性(S1P)相关的脑区特定的花生四烯酸乙醇胺(下调)和鞘氨醇-1-磷酸(上调)调节。
Pflugers Arch. 2024 Dec;476(12):1863-1880. doi: 10.1007/s00424-024-03012-0. Epub 2024 Aug 23.
6
Add-on pramipexole for anhedonic depression: study protocol for a randomised controlled trial and open-label follow-up in Lund, Sweden.附加普拉克索治疗快感缺失性抑郁:在瑞典隆德的一项随机对照试验和开放性随访研究方案。
BMJ Open. 2023 Nov 30;13(11):e076900. doi: 10.1136/bmjopen-2023-076900.
7
Pramipexole for the Treatment of Depression: Efficacy and Mechanisms.普拉克索治疗抑郁症的疗效和机制。
Curr Top Behav Neurosci. 2024;66:49-65. doi: 10.1007/7854_2023_458.
8
Pramipexole Augmentation for Treatment-Resistant Unipolar and Bipolar Depression in the Real World: A Systematic Review and Meta-Analysis.普拉克索增效治疗现实世界中难治性单相和双相抑郁症:一项系统评价和荟萃分析
Life (Basel). 2023 Apr 19;13(4):1043. doi: 10.3390/life13041043.
9
Longitudinal associations between perceived stress and anhedonia during psychotherapy.在心理治疗过程中,感知到的压力与快感缺失之间的纵向关联。
J Affect Disord. 2023 Jun 1;330:206-213. doi: 10.1016/j.jad.2023.03.011. Epub 2023 Mar 11.
10
Stress during puberty exerts sex-specific effects on depressive-like behavior and monoamine neurotransmitters in adolescence and adulthood.青春期的压力对青少年和成年期的抑郁样行为和单胺类神经递质产生性别特异性影响。
Neurobiol Stress. 2022 Oct 3;21:100494. doi: 10.1016/j.ynstr.2022.100494. eCollection 2022 Nov.
对多巴胺激动剂的行为敏化与应激诱导的快感缺失的逆转有关。
Psychopharmacology (Berl). 1993;110(1-2):159-64. doi: 10.1007/BF02246966.
4
Subsensitivity to rewarding and locomotor stimulant effects of a dopamine agonist following chronic mild stress.慢性轻度应激后对多巴胺激动剂奖赏和运动兴奋作用的敏感性降低
Psychopharmacology (Berl). 1993;110(1-2):152-8. doi: 10.1007/BF02246965.
5
Stereospecific reversal of stress-induced anhedonia by mianserin and its (+)-enantiomer.米安色林及其(+)-对映体对应激诱导的快感缺失的立体特异性逆转。
Psychopharmacology (Berl). 1994 Dec;116(4):523-8. doi: 10.1007/BF02247488.
6
Effect of piribedil (ET-495) on plasma norepinephrine: relationship to antidepressant response.吡贝地尔(ET - 495)对血浆去甲肾上腺素的影响:与抗抑郁反应的关系。
Commun Psychopharmacol. 1980;4(3):207-13.
7
Assessing anhedonia in psychiatric patients.评估精神科患者的快感缺乏。
Arch Gen Psychiatry. 1983 Jan;40(1):79-84. doi: 10.1001/archpsyc.1983.01790010081010.
8
Bromocriptine and imipramine in endogenous depression. A double-blind controlled trial in out-patients.溴隐亭与丙咪嗪治疗内源性抑郁症。一项门诊患者双盲对照试验。
J Affect Disord. 1981 Jun;3(2):193-202. doi: 10.1016/0165-0327(81)90044-6.
9
Endogenomorphic depression. A conceptual and terminological revision.内源性抑郁症。概念与术语修订。
Arch Gen Psychiatry. 1974 Oct;31(4):447-54. doi: 10.1001/archpsyc.1974.01760160005001.
10
Dopamine autoreceptor agonists: resolution and pharmacological activity of 2,6-diaminotetrahydrobenzothiazole and an aminothiazole analogue of apomorphine.多巴胺自身受体激动剂:2,6 - 二氨基四氢苯并噻唑及阿扑吗啡的氨基噻唑类似物的拆分与药理活性
J Med Chem. 1987 Mar;30(3):494-8. doi: 10.1021/jm00386a009.