• 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

相似文献

1
Differential effects of chronic antidepressant treatment on shuttle box escape deficits induced by uncontrollable stress.慢性抗抑郁药治疗对不可控应激诱导的穿梭箱逃避缺陷的不同影响。
Psychopharmacology (Berl). 2008 Nov;200(4):585-96. doi: 10.1007/s00213-008-1239-z. Epub 2008 Jul 6.
2
Treatment with escitalopram but not desipramine decreases escape latency times in a learned helplessness model using juvenile rats.在使用幼鼠的习得性无助模型中,艾司西酞普兰而非地昔帕明治疗可缩短逃避潜伏期。
Psychopharmacology (Berl). 2009 Aug;205(2):249-59. doi: 10.1007/s00213-009-1535-2. Epub 2009 Apr 22.
3
Lesions of the basolateral amygdala reverse the long-lasting interference with shuttle box escape produced by uncontrollable stress.外侧下丘脑损伤可逆转不可控应激引起的穿梭箱逃避的长期干扰。
Behav Brain Res. 2010 Jul 29;211(1):71-6. doi: 10.1016/j.bbr.2010.03.012. Epub 2010 Mar 10.
4
Chronic treatment with desipramine: effect on endocrine and behavioral responses induced by inescapable stress.地昔帕明的长期治疗:对不可逃避应激诱导的内分泌和行为反应的影响。
Physiol Behav. 1997 Oct;62(4):939-44. doi: 10.1016/s0031-9384(97)00255-2.
5
Antidepressants reduce inactivity during both inescapable shock administration and shuttle-box testing.抗抑郁药在不可逃避电击给药和穿梭箱测试期间均可减少不动行为。
Eur J Pharmacol. 1991 Nov 5;204(2):187-92. doi: 10.1016/0014-2999(91)90704-t.
6
Behaviour of a genetic mouse model of depression in the learned helplessness paradigm.抑郁遗传小鼠模型在习得性无助范式中的行为表现。
Psychopharmacology (Berl). 2011 Jun;215(3):595-605. doi: 10.1007/s00213-011-2218-3. Epub 2011 Feb 22.
7
Antidepressant activity of the adenosine A2A receptor antagonist, istradefylline (KW-6002) on learned helplessness in rats.腺苷A2A受体拮抗剂异喹啉(KW-6002)对大鼠习得性无助的抗抑郁活性。
Psychopharmacology (Berl). 2014 Jul;231(14):2839-49. doi: 10.1007/s00213-014-3454-0. Epub 2014 Feb 2.
8
Intermittent and continuous swim stress-induced behavioral depression: sensitivity to norepinephrine- and serotonin-selective antidepressants.间歇和连续游泳应激诱导的行为性抑郁:对去甲肾上腺素和 5-羟色胺选择性抗抑郁药的敏感性。
Psychopharmacology (Berl). 2010 Sep;212(1):85-91. doi: 10.1007/s00213-010-1935-3. Epub 2010 Jul 10.
9
The reversal effect of antidepressants on the escape deficit induced by inescapable shock in rats.抗抑郁药对大鼠不可逃避电击所致逃避缺陷的逆转作用。
Psychopharmacology (Berl). 1983;80(3):206-8. doi: 10.1007/BF00436153.
10
Dopaminergic and opioidergic mediations of tricyclic antidepressants in the learned helplessness paradigm.
Pharmacol Biochem Behav. 1999 Nov;64(3):541-8. doi: 10.1016/s0091-3057(99)00102-1.

引用本文的文献

1
A potential candidate for prevention of PTSD: Prazosin prevents learned helplessness behavior in adult male rats.一种预防创伤后应激障碍的潜在候选药物:哌唑嗪可预防成年雄性大鼠的习得性无助行为。
Psychiatry Res. 2025 Jan;343:116283. doi: 10.1016/j.psychres.2024.116283. Epub 2024 Nov 23.
2
The effect of SSRIs on fear learning: a systematic review and meta-analysis.SSRIs 对恐惧学习的影响:系统评价和荟萃分析。
Psychopharmacology (Berl). 2023 Nov;240(11):2335-2359. doi: 10.1007/s00213-023-06333-7. Epub 2023 Feb 27.
3
Blockade of NOP receptor modulates anxiety-related behaviors in mice exposed to inescapable stress.阻断 NOP 受体可调节暴露于不可逃避应激的小鼠的焦虑相关行为。
Psychopharmacology (Berl). 2020 Jun;237(6):1633-1642. doi: 10.1007/s00213-020-05487-y. Epub 2020 Feb 24.
4
Stress induces equivalent remodeling of hippocampal spine synapses in a simulated postpartum environment and in a female rat model of major depression.在模拟产后环境和重度抑郁症雌性大鼠模型中,应激诱导海马棘突突触发生等效重塑。
Neuroscience. 2017 Feb 20;343:384-397. doi: 10.1016/j.neuroscience.2016.12.021. Epub 2016 Dec 22.
5
Modeling postpartum depression in rats: theoretic and methodological issues.大鼠产后抑郁模型:理论与方法学问题
Dongwuxue Yanjiu. 2016 Jul 18;37(4):229-36. doi: 10.13918/j.issn.2095-8137.2016.4.229.
6
Antidepressant activity of nociceptin/orphanin FQ receptor antagonists in the mouse learned helplessness.孤啡肽/孤啡肽FQ受体拮抗剂在小鼠习得性无助中的抗抑郁活性
Psychopharmacology (Berl). 2016 Jul;233(13):2525-32. doi: 10.1007/s00213-016-4310-1. Epub 2016 Apr 30.
7
Restoring mood balance in depression: ketamine reverses deficit in dopamine-dependent synaptic plasticity.恢复抑郁症患者的情绪平衡:氯胺酮可逆转多巴胺依赖性突触可塑性的缺陷。
Biol Psychiatry. 2014 Dec 15;76(12):927-36. doi: 10.1016/j.biopsych.2014.04.014. Epub 2014 May 6.
8
GLYX-13, an NMDA receptor glycine site functional partial agonist enhances cognition and produces antidepressant effects without the psychotomimetic side effects of NMDA receptor antagonists.GLYX-13,一种 NMDA 受体甘氨酸位点功能部分激动剂,可增强认知功能并产生抗抑郁作用,而没有 NMDA 受体拮抗剂的致幻副作用。
Expert Opin Investig Drugs. 2014 Feb;23(2):243-54. doi: 10.1517/13543784.2014.852536. Epub 2013 Nov 20.
9
Decreased expression of synapse-related genes and loss of synapses in major depressive disorder.突触相关基因表达减少和突触丢失在重度抑郁症中的作用。
Nat Med. 2012 Sep;18(9):1413-7. doi: 10.1038/nm.2886.
10
Behaviour of a genetic mouse model of depression in the learned helplessness paradigm.抑郁遗传小鼠模型在习得性无助范式中的行为表现。
Psychopharmacology (Berl). 2011 Jun;215(3):595-605. doi: 10.1007/s00213-011-2218-3. Epub 2011 Feb 22.

本文引用的文献

1
The role of neurotrophic factors in adult hippocampal neurogenesis, antidepressant treatments and animal models of depressive-like behavior.神经营养因子在成体海马神经发生、抗抑郁治疗及类抑郁行为动物模型中的作用
Behav Pharmacol. 2007 Sep;18(5-6):391-418. doi: 10.1097/FBP.0b013e3282ee2aa8.
2
Chronic unpredictable stress decreases cell proliferation in the cerebral cortex of the adult rat.慢性不可预测应激会降低成年大鼠大脑皮质中的细胞增殖。
Biol Psychiatry. 2007 Sep 1;62(5):496-504. doi: 10.1016/j.biopsych.2007.02.006. Epub 2007 Jun 21.
3
Learned helplessness: effects of response requirement and interval between treatment and testing.习得性无助:反应要求以及治疗与测试间隔的影响
Behav Processes. 2007 Nov;76(3):183-91. doi: 10.1016/j.beproc.2007.02.012. Epub 2007 Feb 16.
4
Reversal of learned helplessness by selective serotonin reuptake inhibitors in rats is not dependent on 5-HT availability.选择性5-羟色胺再摄取抑制剂对大鼠习得性无助的逆转作用并不依赖于5-羟色胺的可利用性。
Neuropharmacology. 2007 Mar;52(3):975-84. doi: 10.1016/j.neuropharm.2006.10.014. Epub 2006 Dec 4.
5
Resolving the onset of antidepressants' clinical actions: critical for clinical practice and new drug development.解析抗抑郁药临床作用的起效过程:对临床实践和新药研发至关重要。
J Clin Psychopharmacol. 2006 Dec;26(6):549-53. doi: 10.1097/01.jcp.0000246220.04422.de.
6
Delayed effects of antidepressant drugs in rats.
Behav Pharmacol. 2006 Dec;17(8):641-9. doi: 10.1097/FBP.0b013e3280116ea2.
7
Effect of paroxetine on enhanced contextual fear induced by single prolonged stress in rats.帕罗西汀对大鼠单次长时间应激诱导的情境性恐惧增强的影响。
Psychopharmacology (Berl). 2006 Dec;189(2):165-73. doi: 10.1007/s00213-006-0545-6. Epub 2006 Oct 10.
8
Effects of acute and subchronic treatments with fluoxetine and desipramine on the memory of fear in moderate and high-intensity contextual conditioning.氟西汀和地昔帕明急性及亚慢性治疗对中度和高强度情境条件恐惧记忆的影响。
Eur J Pharmacol. 2006 Aug 7;542(1-3):121-8. doi: 10.1016/j.ejphar.2006.06.019. Epub 2006 Jun 15.
9
Hippocampal cell proliferation regulation by repeated stress and antidepressants.重复应激和抗抑郁药对海马细胞增殖的调节
Neuroreport. 2006 Jun 26;17(9):863-7. doi: 10.1097/01.wnr.0000221827.03222.70.
10
Post-stress facilitation of serotonergic, but not noradrenergic, neurotransmission in the dorsal hippocampus prevents learned helplessness development in rats.应激后促进大鼠背侧海马中5-羟色胺能而非去甲肾上腺素能神经传递可预防习得性无助的发展。
Brain Res. 2006 May 4;1087(1):67-74. doi: 10.1016/j.brainres.2006.03.034. Epub 2006 Apr 19.

慢性抗抑郁药治疗对不可控应激诱导的穿梭箱逃避缺陷的不同影响。

Differential effects of chronic antidepressant treatment on shuttle box escape deficits induced by uncontrollable stress.

作者信息

Valentine Gerald, Dow Antonia, Banasr Mounira, Pittman Brian, Duman Ronald

机构信息

Department of Psychiatry, Yale University, New Haven, CT, USA.

出版信息

Psychopharmacology (Berl). 2008 Nov;200(4):585-96. doi: 10.1007/s00213-008-1239-z. Epub 2008 Jul 6.

DOI:10.1007/s00213-008-1239-z
PMID:18604599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2729428/
Abstract

RATIONALE

The transient behavioral deficit produced in rodents by typical learned helplessness (LH) procedures limits the utility of LH in identifying the therapeutic mechanisms associated with chronic antidepressant administration. In addition, LH procedures do not differentiate between different antidepressant classes as observed in the forced swim test.

OBJECTIVES

To produce both a long lasting and antidepressant reversible behavioral deficit in a modified LH procedure that administers inescapable shock (IS) in the same operant chamber used for shuttle box escape testing.

RESULTS

A single IS session produced a robust increase in the number of escape failures (FR-2 escape contingency) that endured for at least 21 days. This escape deficit was reversed by desipramine (24 mg/kg/day, 6 days) at the first shuttle box session. Fluoxetine (5 mg/kg/day, 6 and 21 days) improved escape performance only after repeated test sessions. In contrast, fluoxetine (5 mg/kg/day, 21 days) completely reversed the first shuttle box test escape deficit induced by exposure to a chronic unpredictable stress procedure devoid of shocks or exposure to operant chambers. These differential drug effects may be due to the presence or absence of contextual cues during escape testing. Repeated re-exposure to the IS context enhanced the FR-2 escape deficit.

CONCLUSIONS

These data suggest that performing escape testing and IS in the same environment improves the preclinical modeling of the time-dependency and behavioral pattern of antidepressant response observed clinically. Additionally, contextual information associated with the IS environment modulates escape performance and may interact differentially with discrete antidepressant classes.

摘要

原理

典型的习得性无助(LH)程序在啮齿动物中产生的短暂行为缺陷限制了LH在识别与慢性抗抑郁药给药相关的治疗机制方面的效用。此外,LH程序无法区分不同类别的抗抑郁药,这在强迫游泳试验中已有观察。

目的

在改良的LH程序中产生一种持久且抗抑郁药可逆转的行为缺陷,该程序在用于穿梭箱逃避测试的同一操作箱中施加不可逃避的电击(IS)。

结果

单次IS会使逃避失败次数(FR-2逃避应急)大幅增加,这种情况持续至少21天。在首次穿梭箱试验时,去甲丙咪嗪(24毫克/千克/天,6天)可逆转这种逃避缺陷。氟西汀(5毫克/千克/天,6天和21天)仅在重复测试后才改善逃避表现。相比之下,氟西汀(5毫克/千克/天,21天)完全逆转了因暴露于无电击的慢性不可预测应激程序或暴露于操作箱而导致的首次穿梭箱测试逃避缺陷。这些不同的药物效应可能归因于逃避测试期间是否存在情境线索。重复重新暴露于IS情境会加剧FR-2逃避缺陷。

结论

这些数据表明,在同一环境中进行逃避测试和IS可改善临床上观察到的抗抑郁反应的时间依赖性和行为模式的临床前模型。此外,与IS环境相关的情境信息调节逃避表现,并且可能与不同类别的抗抑郁药产生不同的相互作用。