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Disruption of prepulse inhibition is associated with compulsive behavior severity and nucleus accumbens dopamine receptor changes in Sapap3 knockout mice.前脉冲抑制破坏与 Sapap3 敲除小鼠强迫行为严重程度和伏隔核多巴胺受体变化有关。
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本文引用的文献

1
The mouse attentional-set-shifting task: a method for assaying successful cognitive aging?老鼠注意定势转移任务:一种检测成功认知老化的方法?
Cogn Affect Behav Neurosci. 2010 May;10(2):243-51. doi: 10.3758/CABN.10.2.243.
2
Correlation of prepulse inhibition and Wisconsin Card Sorting Test in schizophrenia and controls: effects of smoking status.精神分裂症患者及对照组中前脉冲抑制与威斯康星卡片分类测验的相关性:吸烟状况的影响
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Using the MATRICS to guide development of a preclinical cognitive test battery for research in schizophrenia.利用MATRICS指导开发用于精神分裂症研究的临床前认知测试组合。
Pharmacol Ther. 2009 May;122(2):150-202. doi: 10.1016/j.pharmthera.2009.02.004. Epub 2009 Mar 6.
4
On the influence of baseline startle reactivity on the indexation of prepulse inhibition.关于基线惊吓反应性对预脉冲抑制指标的影响
Behav Neurosci. 2008 Aug;122(4):885-900. doi: 10.1037/0735-7044.122.4.885.
5
Atypical antipsychotics clozapine and quetiapine attenuate prepulse inhibition deficits in dopamine transporter knockout mice.非典型抗精神病药物氯氮平和喹硫平可减轻多巴胺转运体基因敲除小鼠的前脉冲抑制缺陷。
Behav Pharmacol. 2008 Sep;19(5-6):562-5. doi: 10.1097/FBP.0b013e32830dc110.
6
Realistic expectations of prepulse inhibition in translational models for schizophrenia research.精神分裂症研究转化模型中对前脉冲抑制的现实期望。
Psychopharmacology (Berl). 2008 Aug;199(3):331-88. doi: 10.1007/s00213-008-1072-4. Epub 2008 Jun 21.
7
Improvement of prepulse inhibition and executive function by the COMT inhibitor tolcapone depends on COMT Val158Met polymorphism.儿茶酚-O-甲基转移酶(COMT)抑制剂托卡朋对预脉冲抑制和执行功能的改善取决于COMT Val158Met基因多态性。
Neuropsychopharmacology. 2008 Dec;33(13):3058-68. doi: 10.1038/npp.2008.82. Epub 2008 Jun 4.
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Cognitive aging and increased distractibility: costs and potential benefits.认知衰老与注意力分散增加:代价与潜在益处
Prog Brain Res. 2008;169:353-63. doi: 10.1016/S0079-6123(07)00022-2.
9
Sensorimotor gating and attentional set-shifting are improved by the mu-opioid receptor agonist morphine in healthy human volunteers.在健康人类志愿者中,μ-阿片受体激动剂吗啡可改善感觉运动门控和注意力转换。
Int J Neuropsychopharmacol. 2008 Aug;11(5):655-69. doi: 10.1017/S1461145707008322. Epub 2008 Jan 16.
10
Prepulse inhibition of the startle reflex and its attentional modulation in the human S-ketamine and N,N-dimethyltryptamine (DMT) models of psychosis.在人类精神分裂症的S-氯胺酮和N,N-二甲基色胺(DMT)模型中,惊吓反射的前脉冲抑制及其注意力调节。
J Psychopharmacol. 2007 May;21(3):312-20. doi: 10.1177/0269881107077734.

小鼠中与年龄相关的跨模态前脉冲抑制改善。

Age-associated improvements in cross-modal prepulse inhibition in mice.

作者信息

Young Jared W, Wallace Chelsea K, Geyer Mark A, Risbrough Victoria B

机构信息

Department of Psychiatry, University of California.

出版信息

Behav Neurosci. 2010 Feb;124(1):133-140. doi: 10.1037/a0018462.

DOI:10.1037/a0018462
PMID:20141288
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3088993/
Abstract

Prepulse inhibition (PPI) is an operational measure of sensorimotor gating that is thought to probe preattentional filtering mechanisms. PPI is deficient in several neuropsychiatric disorders, possibly reflecting abnormalities in frontal-cortical-striatal circuitry. Several studies support the predictive validity of animal PPI to model human sensorimotor gating phenomena but only limited studies have addressed the effects of aging. Studies in humans suggest that PPI is improved or unaffected as humans age (>60 years) and does not correlate with cognitive decline in aged populations. Rodent studies to date, however, suggest that PPI declines with age. Here we tested the hypothesis that PPI measures in rodents are sensitive to stimulus modality, with the prediction that intact sensory modalities in aged animals would be predictive of aging-induced increases in PPI. To test our hypothesis, we assessed PPI using acoustic, tactile, and visual prepulses in young (4 month) and old (23 month) C57BL/6N mice. Consistent with data across species, we observed reduced startle reactivity in older mice. Aging effects on PPI interacted significantly with prepulse modality, with deficient acoustic PPI but increased visual and tactile PPI in aged animals. These data are therefore consistent with PPI studies in older humans when controlling for hearing impairments. The results are discussed in terms of 1) cross-species translational validity for mouse PPI testing, 2) the need for startle reactivity differences to be accounted for in PPI analyses, and 3) the utility of cross-modal PPI testing in subjects where hearing loss has been documented.

摘要

前脉冲抑制(PPI)是一种感觉运动门控的操作性测量方法,被认为可探测注意前过滤机制。PPI在几种神经精神疾病中存在缺陷,可能反映了额叶 - 皮质 - 纹状体回路的异常。多项研究支持动物PPI对模拟人类感觉运动门控现象的预测效度,但仅有有限的研究探讨了衰老的影响。对人类的研究表明,随着人类年龄增长(>60岁),PPI得到改善或未受影响,且与老年人群的认知衰退无关。然而,迄今为止的啮齿动物研究表明,PPI会随着年龄下降。在此,我们检验了这样一个假设,即啮齿动物中的PPI测量对刺激模式敏感,预计老年动物完整的感觉模式可预测衰老引起的PPI增加。为了检验我们的假设,我们在年轻(4个月)和年老(23个月)的C57BL/6N小鼠中使用听觉、触觉和视觉前脉冲评估PPI。与跨物种数据一致,我们观察到老年小鼠的惊吓反应性降低。衰老对PPI的影响与前脉冲模式有显著交互作用,老年动物的听觉PPI存在缺陷,但视觉和触觉PPI增加。因此,在控制听力损伤时,这些数据与对老年人的PPI研究一致。我们从以下几个方面讨论了结果:1)小鼠PPI测试的跨物种翻译效度,2)在PPI分析中需要考虑惊吓反应性差异,3)在已记录听力损失的受试者中进行跨模态PPI测试的效用。