• 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

诱发多饮症作为强迫行为的模型:神经药理学和神经内分泌基础。

Schedule-induced polydipsia as a model of compulsive behavior: neuropharmacological and neuroendocrine bases.

机构信息

Departmento de Neurociencia y Ciencias de la Salud, Universidad de Almería, Carretera de Sacramento s/n, La Cañada de San Urbano, 04120 Almeria, Spain.

出版信息

Psychopharmacology (Berl). 2012 Jan;219(2):647-59. doi: 10.1007/s00213-011-2570-3. Epub 2011 Nov 24.

DOI:10.1007/s00213-011-2570-3
PMID:22113447
Abstract

BACKGROUND

Schedule-induced polydipsia (SIP), characterized by the development of excessive drinking under intermittent food-reinforcement schedules, has been proposed as a successful model for obsessive-compulsive disorder (OCD), schizophrenia, and alcohol abuse.

OBJECTIVES

The purpose of this study was to review the main findings and current thinking regarding the use of SIP for compulsivity assessment and evaluate its contribution to improving our knowledge of the neurobehavioral mechanisms underlying the excessive behavior manifested in SIP relevant to compulsive behavior disorders.

METHODS

The literature reviews SIP procedure and surveys main findings about its neurobehavioral basis and pharmacology relevant to its possible status as a model for compulsive disorders. Specifically, we reviewed effects of antipsychotics and serotoninergic drugs used in the treatment of OCD and schizophrenia. We also considered individual differences in SIP and its relevance as a possible compulsivity endophenotype.

CONCLUSIONS

SIP represents an animal model of non-regulatory and excessive drinking that may be valid for studying the psychopharmacology of the compulsive phenotype and modeling different psychopathologies from compulsivity spectrum disorders.

摘要

背景

间歇性食物强化程序诱发的多饮(SIP)的特征是在间歇性食物强化程序下发展出过度饮酒,被提议作为强迫症(OCD)、精神分裂症和酒精滥用的成功模型。

目的

本研究的目的是回顾关于 SIP 用于评估强迫性的主要发现和当前思路,并评估其对我们了解 SIP 相关过度行为的神经行为机制的贡献,这些过度行为与强迫性行为障碍有关。

方法

文献回顾了 SIP 程序,并调查了其神经行为基础和与强迫症相关的药理学的主要发现,特别是我们回顾了抗精神病药和用于治疗 OCD 和精神分裂症的血清素能药物的作用。我们还考虑了 SIP 的个体差异及其作为可能的强迫性内表型的相关性。

结论

SIP 代表一种非调节性和过度饮酒的动物模型,可能对研究强迫表型的精神药理学以及建模不同的精神病理学从强迫性谱系障碍有价值。

相似文献

1
Schedule-induced polydipsia as a model of compulsive behavior: neuropharmacological and neuroendocrine bases.诱发多饮症作为强迫行为的模型:神经药理学和神经内分泌基础。
Psychopharmacology (Berl). 2012 Jan;219(2):647-59. doi: 10.1007/s00213-011-2570-3. Epub 2011 Nov 24.
2
Behavioral and biological markers for predicting compulsive-like drinking in schedule-induced polydipsia.预测习惯性多饮症中强迫性饮酒行为和生物学标志物。
Prog Neuropsychopharmacol Biol Psychiatry. 2019 Jul 13;93:149-160. doi: 10.1016/j.pnpbp.2019.03.016. Epub 2019 Mar 30.
3
Differential Neurobiological Markers in Phenotype-stratified Rats Modeling High or Low Vulnerability to Compulsive Behavior: A Narrative Review.表型分层大鼠模型中对强迫行为高或低易感性的差异神经生物学标志物:综述。
Curr Neuropharmacol. 2023;21(9):1924-1933. doi: 10.2174/1570159X21666221121091454.
4
Poor inhibitory control and neurochemical differences in high compulsive drinker rats selected by schedule-induced polydipsia.通过习惯性多饮诱发选择的高强迫性饮酒大鼠存在抑制控制能力差和神经化学差异。
Psychopharmacology (Berl). 2012 Jan;219(2):661-72. doi: 10.1007/s00213-011-2575-y. Epub 2011 Nov 24.
5
Increased amygdala and decreased hippocampus volume after schedule-induced polydipsia in high drinker compulsive rats.在高饮酒强迫大鼠的习惯性多饮诱导后,杏仁核体积增加,海马体体积减小。
Behav Brain Res. 2020 Jul 15;390:112592. doi: 10.1016/j.bbr.2020.112592. Epub 2020 May 14.
6
Socioemotional deficit and HPA axis time response in high compulsive rats selected by schedule-induced polydipsia.高强迫性大鼠通过诱导性多饮选择的社会情感缺陷和 HPA 轴时间反应。
Horm Behav. 2022 Jun;142:105170. doi: 10.1016/j.yhbeh.2022.105170. Epub 2022 Mar 31.
7
Do psychoactive drugs have a therapeutic role in compulsivity? Studies on schedule-induced polydipsia.在强迫性问题上,精神活性药物是否具有治疗作用?关于习惯性多饮症的研究。
Psychopharmacology (Berl). 2018 Feb;235(2):419-432. doi: 10.1007/s00213-017-4819-y. Epub 2018 Jan 8.
8
Increased Fear Memory and Glutamatergic Modulation in Compulsive Drinker Rats Selected by Schedule-Induced Polydipsia.通过程序诱导多饮选择的强迫性饮酒大鼠的恐惧记忆增强和谷氨酸能调节
Front Behav Neurosci. 2019 May 7;13:100. doi: 10.3389/fnbeh.2019.00100. eCollection 2019.
9
Behavioral Biomarkers of Schizophrenia in High Drinker Rats: A Potential Endophenotype of Compulsive Neuropsychiatric Disorders.精神分裂症行为生物标志物在高饮酒大鼠中的研究:强迫性神经精神疾病的潜在内表型。
Schizophr Bull. 2017 Jul 1;43(4):778-787. doi: 10.1093/schbul/sbw141.
10
Schedule-induced polydipsia is associated with increased spine density in dorsolateral striatum neurons.日程诱导的烦渴与背外侧纹状体神经元中脊柱密度增加有关。
Neuroscience. 2015 Aug 6;300:238-45. doi: 10.1016/j.neuroscience.2015.05.026. Epub 2015 May 16.

引用本文的文献

1
Sex differences in compulsive alcohol drinking phenotypes: implications for decision-making and social behavior in a preclinical model.强迫性饮酒表型中的性别差异:对临床前模型中决策和社会行为的影响。
Psychopharmacology (Berl). 2025 Sep 16. doi: 10.1007/s00213-025-06895-8.
2
Increased Neuroplasticity in Frontal Cortex to Reduce Compulsive Behavior: A Preclinical tDCS Study in Male Rats.增加前额叶皮质的神经可塑性以减少强迫行为:一项雄性大鼠的临床前经颅直流电刺激研究
Mol Neurobiol. 2025 Jul 23. doi: 10.1007/s12035-025-05218-4.
3
Anxiolytic-like effects of the dual orexin receptor antagonist daridorexant in rats.

本文引用的文献

1
Poor inhibitory control and neurochemical differences in high compulsive drinker rats selected by schedule-induced polydipsia.通过习惯性多饮诱发选择的高强迫性饮酒大鼠存在抑制控制能力差和神经化学差异。
Psychopharmacology (Berl). 2012 Jan;219(2):661-72. doi: 10.1007/s00213-011-2575-y. Epub 2011 Nov 24.
2
Schedule-induced polydipsia in the spontaneously hypertensive rat and its relation to impulsive behaviour.自发性高血压大鼠的诱导性多饮症及其与冲动行为的关系。
Behav Brain Res. 2011 Sep 30;223(1):58-69. doi: 10.1016/j.bbr.2011.04.017. Epub 2011 Apr 21.
3
Translational approaches to obsessive-compulsive disorder: from animal models to clinical treatment.
双重食欲素受体拮抗剂达立多雷生对大鼠的抗焦虑样作用。
Neurosci Appl. 2024 Mar 16;3:104056. doi: 10.1016/j.nsa.2024.104056. eCollection 2024.
4
Optogenetic Stimulation of Novel Tph2-Cre Rats Advances Insight into Serotonin's Role in Locomotion, Reinforcement, and Compulsivity.新型Tph2-Cre大鼠的光遗传学刺激增进了对血清素在运动、强化和强迫行为中作用的理解。
J Neurosci. 2025 May 21;45(21):e1424242025. doi: 10.1523/JNEUROSCI.1424-24.2025.
5
From Nutritional Patterns to Behavior: High-Fat Diet Influences on Inhibitory Control, Brain Gene Expression, and Metabolomics in Rats.从营养模式到行为:高脂饮食对大鼠抑制控制、脑基因表达和代谢组学的影响
ACS Chem Neurosci. 2024 Dec 18;15(24):4369-4382. doi: 10.1021/acschemneuro.4c00297. Epub 2024 Nov 28.
6
Characterization in the rat of the individual tendency to rely on alcohol to cope with distress and the ensuing vulnerability to drink compulsively.对大鼠个体依赖酒精来应对痛苦的倾向以及随之而来的强迫性饮酒易感性的特征描述。
Brain Commun. 2024 May 14;6(3):fcae169. doi: 10.1093/braincomms/fcae169. eCollection 2024.
7
Repeated Δ-9-Tetrahydrocannabinol administration dose dependently increases stablished schedule-induced drinking.反复给予 Δ-9-四氢大麻酚给药剂量依赖性地增加既定的条件性饮水。
Psychopharmacology (Berl). 2024 Jun;241(6):1277-1286. doi: 10.1007/s00213-024-06563-3. Epub 2024 Feb 28.
8
Mapping the neuroanatomical abnormalities in a phenotype of male compulsive rats.绘制雄性强迫性大鼠表型的神经解剖异常图谱。
Behav Brain Funct. 2023 Nov 6;19(1):19. doi: 10.1186/s12993-023-00221-y.
9
From Reward to Anhedonia-Dopamine Function in the Global Mental Health Context.从奖励到快感缺失——全球心理健康背景下的多巴胺功能
Biomedicines. 2023 Sep 6;11(9):2469. doi: 10.3390/biomedicines11092469.
10
Reduced Expression of the Htr2a, Grin1, and Bdnf Genes and Cognitive Inflexibility in a Model of High Compulsive Rats.在一种强迫性高的大鼠模型中,Htr2a、Grin1 和 Bdnf 基因表达减少与认知灵活性降低有关。
Mol Neurobiol. 2023 Dec;60(12):6975-6991. doi: 10.1007/s12035-023-03506-5. Epub 2023 Jul 31.
强迫症的转化研究方法:从动物模型到临床治疗。
Br J Pharmacol. 2011 Oct;164(4):1044-61. doi: 10.1111/j.1476-5381.2011.01422.x.
4
Dopamine dynamics associated with, and resulting from, schedule-induced alcohol self-administration: analyses in dopamine transporter knockout mice.与 及 源自 时间表诱导的酒精自我给药相关的多巴胺动态:多巴胺转运体敲除小鼠的分析。
Alcohol. 2011 Jun;45(4):325-39. doi: 10.1016/j.alcohol.2010.12.006. Epub 2011 Feb 26.
5
Impulsivity, compulsivity, and top-down cognitive control.冲动性、强迫性和自上而下的认知控制。
Neuron. 2011 Feb 24;69(4):680-94. doi: 10.1016/j.neuron.2011.01.020.
6
Animal models of neuropsychiatric disorders.神经精神疾病的动物模型。
Annu Rev Clin Psychol. 2011;7:39-61. doi: 10.1146/annurev-clinpsy-032210-104454.
7
Effects of aripiprazole, olanzapine, and haloperidol in a model of cognitive deficit of schizophrenia in rats: relationship with glutamate release in the medial prefrontal cortex.阿立哌唑、奥氮平、氟哌啶醇对精神分裂症认知缺陷大鼠模型的影响:与内侧前额叶皮质谷氨酸释放的关系。
Psychopharmacology (Berl). 2011 Apr;214(3):639-52. doi: 10.1007/s00213-010-2065-7. Epub 2010 Nov 4.
8
Sertindole restores attentional performance and suppresses glutamate release induced by the NMDA receptor antagonist CPP.赛曲哚尔恢复 NMDA 受体拮抗剂 CPP 诱导的注意力表现和抑制谷氨酸释放。
Psychopharmacology (Berl). 2011 Apr;214(3):625-37. doi: 10.1007/s00213-010-2066-6. Epub 2010 Nov 4.
9
Individual differences in schedule-induced polydipsia: neuroanatomical dopamine divergences.个体在时间诱导性多饮症方面的差异:神经解剖学多巴胺分歧。
Behav Brain Res. 2011 Feb 2;217(1):195-201. doi: 10.1016/j.bbr.2010.10.010. Epub 2010 Oct 23.
10
Increased schedule-induced polydipsia in the rat following subchronic treatment with MK-801.亚慢性 MK-801 处理后大鼠的条件性饮水增加。
Schizophr Res. 2011 Jan;125(1):93-8. doi: 10.1016/j.schres.2010.07.022. Epub 2010 Aug 16.