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The GRIA1 AMPA receptor subunit and selective learning GRIA1 AMPA受体亚基与选择性学习。
IF 1.8 4区 心理学 Q3 BEHAVIORAL SCIENCES Pub Date : 2025-08-16 DOI: 10.1016/j.nlm.2025.108089
Jasmin A. Strickland , Joseph M. Austen , Rolf Sprengel , David J. Sanderson
The GRIA1 subunit of the AMPA receptor, encoded by the GRIA1 gene, has been implicated in schizophrenia. Schizophrenia is associated with impairments in attention that may lead to other symptoms due to a failure to learn selectively (e.g., learning about redundant cues). In mice, gene-targeted inactivation of GRIA1 impairs hippocampal synaptic plasticity and alters learning and memory. To test the role of GRIA1 in selective learning, we trained mice lacking GRIA1 on the blocking procedure. GRIA1 knockout mice showed normal blocking of appetitive Pavlovian conditioning, in which prior learning of an auditory cue reduced subsequent acquisition of conditioned responding to a visual cue when the two cues were trained in compound. GRIA1 knockout mice, however, failed to show blocking of flavour preference conditioning despite normal learning of the flavour that, in contrast, was effective in blocking conditioning in control mice. This impairment occurred under conditions in which mice were exposed to one flavour a day and when exposed to two flavours a day to aid discrimination between flavours. The dissociation between learning with visual cues and learning with flavours may suggest that GRIA1 containing AMPA receptors are necessary for selective learning for particular stimulus modalities. Alternatively, GRIA1 may play a role in selective learning when the similarity between cues competing for learning is high, as for flavour preference learning, but not when low, as for auditory and visual cues.
由GRIA1基因编码的AMPA受体GRIA1亚基与精神分裂症有关。精神分裂症与注意力障碍有关,注意力障碍可能由于不能选择性地学习(例如,学习多余的线索)而导致其他症状。在小鼠中,基因靶向的GRIA1失活会损害海马突触可塑性并改变学习和记忆。为了测试GRIA1在选择性学习中的作用,我们对缺乏GRIA1的小鼠进行了阻断过程的训练。GRIA1基因敲除小鼠表现出正常的食欲巴甫洛夫条件反射阻滞,即当两种线索被复合训练时,先前对听觉线索的学习减少了随后对视觉线索的条件反应获得。然而,GRIA1基因敲除小鼠未能显示出风味偏好条件反射的阻断,尽管正常的风味学习,相比之下,在对照小鼠中有效地阻断了条件反射。这种损伤发生在老鼠每天接触一种味道和每天接触两种味道以帮助区分味道的条件下。视觉学习和味觉学习之间的分离可能表明,含有AMPA受体的GRIA1对于特定刺激模式的选择性学习是必要的。另外,当竞争学习的线索之间的相似性很高时,GRIA1可能在选择性学习中发挥作用,比如味道偏好学习,但当听觉和视觉线索之间的相似性较低时,GRIA1可能不起作用。
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引用次数: 0
The role of retinoids in memory reconsolidation and extinction following appetitive conditioning 类维生素a在食欲调节后记忆重新巩固和消退中的作用。
IF 1.8 4区 心理学 Q3 BEHAVIORAL SCIENCES Pub Date : 2025-07-30 DOI: 10.1016/j.nlm.2025.108079
Justin Wimmer , Zakariah Ibrahim , Gaynor E. Spencer
Retinoic acid, the active metabolite of vitamin A, is an important signaling molecule during vertebrate synaptic plasticity and learning and memory. We have shown that it also plays a role in long-term memory formation following both operant and classical conditioning in the invertebrate, Lymnaea stagnalis. Following retrieval, recent long-term memories can undergo additional processing whereby they can be updated and re-stabilized during reconsolidation, or suppressed during extinction. Here, we examined whether retinoic acid is involved in post-retrieval memory processing by utilizing appetitive classical conditioning of Lymnaea. We show that exposure to retinoid signaling inhibitors differentially disrupts memory reconsolidation, depending on the need for protein synthesis and the extent of training received. We also show that memory extinction is inhibited in the presence of both retinoid inhibitors and protein synthesis inhibitors, regardless of the extent of training. These findings suggest that retinoids play a role in the continued processing of implicit memories following retrieval.
维甲酸是维生素A的活性代谢物,是脊椎动物突触可塑性和学习记忆过程中的重要信号分子。我们已经证明,它也在无脊椎动物(lynaea stagnation)的操作性条件反射和经典条件反射后的长期记忆形成中发挥作用。在检索之后,最近的长期记忆可以经历额外的加工,从而在重新巩固期间更新和重新稳定,或在消失期间被抑制。在这里,我们研究维甲酸是否参与提取后记忆加工,利用食欲经典条件反射的淋巴细胞。我们表明,暴露于类视黄醛信号抑制剂会不同程度地破坏记忆再巩固,这取决于蛋白质合成的需要和接受的训练程度。我们还表明,无论训练程度如何,在类视黄醛抑制剂和蛋白质合成抑制剂的存在下,记忆消退都受到抑制。这些发现表明类维生素a在提取后内隐记忆的继续加工中起作用。
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引用次数: 0
The effect of post-learning rest on false memory 学习后休息对错误记忆的影响。
IF 1.8 4区 心理学 Q3 BEHAVIORAL SCIENCES Pub Date : 2025-07-27 DOI: 10.1016/j.nlm.2025.108080
William H. Livingston , Adam L. Putnam , Erin J. Wamsley
Like sleep, a brief period of eyes-closed waking rest following encoding can improve memory. But in addition to quantitatively strengthening memory, sleep also qualitatively transforms memory. In one example of this effect, sleep has been reported to promote the formation of false memory, perhaps as a result of preferentially strengthening gist memory over memory for veridical detail. Here, we tested whether a period of eyes-closed waking rest, like sleep, affects the formation of false memories. We hypothesized that rest would increase false memory in the Deese-Roediger-McDermott (DRM) paradigm as measured by recall but would decrease false memory as measured by recognition. Following auditory encoding of 8 DRM word lists, N = 51 participants either sat quietly with their eyes closed for 15 min or spent an equivalent period completing a distractor task (within-subjects). Afterwards, participants completed a recall and recognition test. Despite being well-powered to detect effects of the magnitude previously reported in sleep studies, we did not detect any effect of rest on the formation of false memories, regardless of testing method. This may indicate that waking rest does not affect the formation of false memories in the same way that sleep does.
就像睡觉一样,编码后的短暂闭眼休息可以提高记忆力。但是除了从数量上加强记忆,睡眠也从质量上改变记忆。在这种效应的一个例子中,据报道,睡眠可以促进错误记忆的形成,这可能是由于优先加强要点记忆而不是真实细节的记忆。在这里,我们测试了一段闭眼的清醒休息是否会影响错误记忆的形成,就像睡觉一样。我们假设休息会增加用回忆来衡量的Deese-Roediger-McDermott (DRM)范式中的错误记忆,但会减少用识别来衡量的错误记忆。在对8个DRM单词列表进行听觉编码后,N = 51名参与者要么闭着眼睛安静地坐着15 分钟,要么花相同的时间完成一项分散注意力的任务(在受试者中)。之后,参与者完成了回忆和识别测试。尽管我们有能力检测到之前在睡眠研究中报道的影响程度,但无论采用何种测试方法,我们都没有发现休息对错误记忆形成的任何影响。这可能表明,清醒时的休息不会像睡眠那样影响错误记忆的形成。
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引用次数: 0
Male spontaneously hypertensive rats demonstrate reduced goal-directed control and difficulty updating previous learning 雄性自发性高血压大鼠表现出目标导向控制能力下降和更新先前学习的困难
IF 1.8 4区 心理学 Q3 BEHAVIORAL SCIENCES Pub Date : 2025-07-26 DOI: 10.1016/j.nlm.2025.108078
Zachary Pierce-Messick, Elif Sari, Laura H. Corbit
Habitual control of repeated behaviours is adaptive because it can allow routine behaviours to continue under conditions where cognitive capacity is limited or burdened. However, the impact that cognitive demand has on behavioural control has not been thoroughly studied in animal models of habits. This study used a strain of rats—spontaneously hypertensive rats (SHRs)—that have known cognitive deficits to investigate their ability to update their behaviour following changes to outcome value, instrumental contingency, and the predictions of stimuli across multiple tasks. An outcome devaluation task was used to test whether instrumental performance was sensitive to changes in outcome value. While SHRs reduced responding for the devalued outcome, this effect was dampened relative to Long Evans controls. An omission contingency was then introduced and SHRs were unable to adapt their responding when a once reinforced response now prevented the delivery of a free outcome. A Pavlovian devaluation task found that SHRs were insensitive to devaluation and entered the magazine upon presentation of a reward-predictive stimulus, regardless of whether the stimulus predicted a devalued or non-devalued outcome. Finally, SHRs were found to be slower than Long Evans to inhibit initial learning when a stimulus that initially predicted food pellets was no longer reinforced. Collectively, these tasks help better characterize the behavioural capabilities of SHRs and extends our understanding of how limited cognitive capacity relates to expression of habitual behaviour.
对重复行为的习惯性控制是适应性的,因为它可以让常规行为在认知能力有限或有负担的情况下继续下去。然而,认知需求对行为控制的影响尚未在动物习惯模型中得到充分研究。这项研究使用了一种已知认知缺陷的大鼠——自发性高血压大鼠(SHRs),研究它们在结果值、工具偶然性和多任务刺激预测变化后更新行为的能力。结果贬值任务用于测试工具性能是否对结果值的变化敏感。虽然SHRs降低了对贬值结果的反应,但相对于Long Evans对照,这种影响受到抑制。随后引入了遗漏偶然性,当曾经得到强化的反应现在阻碍了自由结果的交付时,SHRs无法调整自己的反应。巴甫洛夫贬值任务发现,SHRs对贬值不敏感,并在出现奖励预测刺激时进入杂志,无论刺激预测的结果是贬值还是非贬值。最后,当最初预测食物颗粒的刺激不再加强时,SHRs被发现比Long Evans更慢地抑制初始学习。总的来说,这些任务有助于更好地描述SHRs的行为能力,并扩展我们对有限的认知能力与习惯性行为表达之间的关系的理解。
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引用次数: 0
Neuro-immune interactions in memory 记忆中的神经免疫相互作用。
IF 2.2 4区 心理学 Q3 BEHAVIORAL SCIENCES Pub Date : 2025-07-11 DOI: 10.1016/j.nlm.2025.108077
E. Stewart , T.J. Ryan
Responding appropriately to both internal and external factors to maintain homeostasis is key to survival in a dynamic environment. Memory is an adaptive brain function that enables organisms to interact efficiently with their environment by processing and storing perceptual input. Memory functions by shaping behaviour in the present, based on past experiences. These experiences are defined by both external environmental cues and internal signals (physiological states) and these dual sources of information require integration and feedback between central and peripheral systems. The immune system is a key physiological system that works to protect against pathogens and maintain homeostasis, and can also mediate behavioural changes through communication with the brain. Here we review the dynamic relationship between memory and the immune system in both health and disease.
在我们生活的动态环境中,适当地对内外因素作出反应以保持体内平衡是生存的关键。记忆是一种高度适应性的大脑功能,它使生物体能够通过处理和存储感知输入来有效地与环境互动。记忆根据过去的经验塑造现在的行为。这些体验是由外部环境线索和内部信号(生理状态)定义的,这需要中枢和外围系统之间的整合和反馈。免疫系统是一个关键的生理系统,它可以防止病原体和维持体内平衡,并可以通过与大脑的交流来调节行为变化。在这里,我们回顾记忆和免疫系统在健康和疾病之间的动态关系。
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引用次数: 0
The role of post-learning EEG theta/beta ratio in long-term navigation performance 学习后脑电图θ / β比值在长期导航表现中的作用
IF 2.2 4区 心理学 Q3 BEHAVIORAL SCIENCES Pub Date : 2025-06-25 DOI: 10.1016/j.nlm.2025.108076
Roman Rozengurt , Alexandra Doljenko , Daniel A. Levy , Avi Mendelsohn
Memory consolidation processes have been shown to benefit from modulations in brain activity, particularly theta oscillations. Our previous studies showed that increases in post-learning Theta/Beta power ratio improves subsequent performance in both procedural and declarative memory across various tasks. In this study, we investigated the role of increases in frontal-midline Theta/Beta power ratio using EEG neurofeedback (NFB) in enhancing spatial memory consolidation during a navigation task in a virtual Minecraft environment. Sixty-four participants were randomly assigned to one of three groups: Theta/Beta NFB, Beta/Theta NFB, or a passive control group. Following spatial memory acquisition and three memory tests in the virtual environment, participants underwent a neurofeedback intervention designed to either upregulating or downregulate the Theta/Beta power ratio. Performance was assessed immediately post-intervention, 24 h later, and one week after the intervention. Results indicate that while some participants failed to regulate their Theta/Beta power by using the NFB display, those who increased their Theta/Beta power ratio, regardless of NFB, showed improved spatial memory, reflected in faster task completion times. Conversely, participants who exhibited a decrease in Theta/Beta ratio showed performance declines, while the passive control group showed minimal improvement. Although all participants improved over time, participants who increased Theta/Beta ratio showed the most substantial gains. These findings highlight the importance of post-learning Theta/Beta ratio oscillations in spatial memory consolidation. The study’s implications extend to clinical neuromodulation applications and a deeper understanding of memory processes.
记忆巩固过程已被证明受益于大脑活动的调节,特别是θ波振荡。我们之前的研究表明,学习后Theta/Beta能量比的增加提高了在各种任务中的程序记忆和陈述性记忆的后续表现。在这项研究中,我们利用脑电图神经反馈(NFB)研究了在虚拟《我的世界》环境中导航任务中,额中线θ / β功率比的增加在增强空间记忆巩固中的作用。64名参与者被随机分配到三组中的一组:Theta/Beta NFB, Beta/Theta NFB或被动对照组。在空间记忆获取和虚拟环境中的三次记忆测试之后,参与者接受了旨在上调或下调Theta/Beta功率比的神经反馈干预。在干预后立即、24小时后和干预后一周评估表现。结果表明,虽然一些参与者没有通过使用非视觉效果来调节他们的Theta/Beta功率,但那些提高了Theta/Beta功率比的参与者,无论是否使用非视觉效果,都表现出了空间记忆的改善,这反映在更快的任务完成时间上。相反,Theta/Beta比值下降的参与者表现出表现下降,而被动控制组表现出微小的改善。虽然所有的参与者随着时间的推移都有所改善,但增加Theta/Beta比率的参与者表现出最显著的进步。这些发现强调了学习后Theta/Beta比值振荡在空间记忆巩固中的重要性。这项研究的意义延伸到临床神经调节应用和对记忆过程的更深层次的理解。
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引用次数: 0
Increasing degradation-independent linear polyubiquitin in the hippocampus enhances memory in young adult but not aged rats 海马中退化无关的线性多泛素的增加增强了年轻成年大鼠的记忆,而不是老年大鼠
IF 2.2 4区 心理学 Q3 BEHAVIORAL SCIENCES Pub Date : 2025-06-20 DOI: 10.1016/j.nlm.2025.108075
Morgan B. Patrick , Natalie J. Preveza , Yeeun Bae , Harshini Venkat , Olivia N. Ball , Gueladouan Setenet , Shannon E. Kincaid , Jennifer R. Abraham , Adam Cummings , Anna Rubley , W. Keith Ray , Richard F. Helm , Timothy J. Jarome
Age-related memory loss affects approximately 40% of the world’s population after the age of 65 and is a significant risk factor for the development of dementia and Alzheimer’s Disease (AD). Numerous studies have reported that late in life there decreases in the function of the ubiquitin–proteasome system, the main regulator of protein degradation in cells that is also critically involved in memory formation. However, ubiquitin can mark proteins for fates other than destruction by the proteasome. Importantly, it remains unknown how the aging process alters proteasome-independent forms of ubiquitination and how this could contribute to age-related memory loss. Here, using an unbiased proteomic approach, we found that linear polyubiquitination – the only non-lysine proteasome-independent form of polyubiquitination – is significantly increased in the aged hippocampus at rest relative to young adults. However, in response to learning there was a significant reduction in linear polyubiquitination in the aged hippocampus, which contrasted with increases seen in young adult animals following learning. CRISPR-dCas9 mediated upregulation of linear polyubiquitination in the hippocampus improved memory in young adult, but not aged, rats. Together, these data suggest that while linear polyubiquitination is a critical regulator of hippocampus-dependent memory, increasing it in the aged hippocampus is not sufficient to improve memory in advanced age. These findings advance our understanding of the molecular mechanisms regulating memory late in life and stimulate future research on the role of degradation-independent ubiquitination in this process.
与年龄相关的记忆丧失影响着65岁以后世界上大约40%的人口,是痴呆症和阿尔茨海默病(AD)发展的一个重要危险因素。大量研究表明,在生命的后期,泛素-蛋白酶体系统的功能会下降,泛素-蛋白酶体系统是细胞中蛋白质降解的主要调节因子,也与记忆的形成密切相关。然而,泛素可以标记蛋白质的命运,而不是被蛋白酶体破坏。重要的是,我们仍然不知道衰老过程是如何改变蛋白酶体独立形式的泛素化,以及这如何导致与年龄相关的记忆丧失。在这里,使用无偏倚的蛋白质组学方法,我们发现线性多泛素化——唯一非赖氨酸蛋白酶体独立的多泛素化形式——在静止的老年海马中比年轻人显著增加。然而,在学习的反应中,老年海马的线性多泛素化显著减少,与学习后年轻成年动物的线性多泛素化增加形成对比。CRISPR-dCas9介导的海马线性多泛素化上调改善了年轻成年大鼠的记忆,但没有改善老年大鼠的记忆。总之,这些数据表明,尽管线性多泛素化是海马体依赖性记忆的关键调节因子,但在老年海马体中增加线性多泛素化并不足以改善老年人的记忆。这些发现促进了我们对生命后期调节记忆的分子机制的理解,并刺激了未来对降解无关泛素化在这一过程中的作用的研究。
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引用次数: 0
Frustrative nonreward, sucrose consumption, and the basal ganglia: Role of chemogenetic activation of projections from the nucleus accumbens to the globus pallidus internus, globus pallidus externus, and ventral pallidum 挫折性无奖赏、蔗糖消耗和基底神经节:伏隔核向内苍白球、外苍白球和腹侧苍白球投射的化学激活的作用
IF 2.2 4区 心理学 Q3 BEHAVIORAL SCIENCES Pub Date : 2025-06-18 DOI: 10.1016/j.nlm.2025.108073
Christopher W. Hagen, Jessica Suárez, Mauricio R. Papini
Mammals experience negative emotions after the unexpected reduction in reward magnitude—called frustrative nonreward (FNR). The neurobiological mechanisms activated in response to unexpected reward downshift could shed light on loss-induced anxiety, conflict, mood, and physical pain. Experiment 1 examined the role of three basal ganglia (BG) pathways in the adjustment to unexpected sucrose downshifts. A double-infection chemogenetic procedure was used to activate neurons in the nucleus accumbens (NAc) that project to the globus pallidus externus (GPe), globus pallidus internus (GPi), or ventral pallidum (VP) during a 32-to-2% sucrose downshift. Activation of the NAc-to-GPe pathway had no observable effects on licking during reward downshift, whereas activation of either the NAc-to-GPi or NAc-to-VP pathways caused significant consummatory suppression. Chemogenetic activation of the NAc-to-GPi and NAc-to-VP pathways also yielded increased consummatory suppression in animals exposed to either 2% sucrose (Experiment 2) or 32% sucrose (Experiment 3) in the absence of a sucrose downshift. These effects were accompanied by no evidence of motor dysfunction in the open field and a nonsignificant trend toward a decrease in sucrose palatability, particularly with a choice between 2% sucrose and water. However, preliminary observations show that licking suppression after CNO injections also enhanced activity in the conditioning box during access to 32% sucrose and relative to vehicle injections. Thus, these BG pathways regulate consummatory behavior in different ways, but whether BG dysfunction influences the behavioral response to unexpected reward downshifts remains to be established.
哺乳动物在奖励量意外减少后会经历负面情绪,这被称为挫折性无奖励(FNR)。意想不到的奖励下降反应激活的神经生物学机制可以揭示损失引起的焦虑、冲突、情绪和身体疼痛。实验1考察了基底节区(BG)的三条通路在调节非预期的蔗糖下降中的作用。采用双重感染化学发生程序,激活伏隔核(NAc)中的神经元,这些神经元在32- 2%蔗糖降速期间投射到外白球(GPe)、内白球(GPi)或腹侧白球(VP)。在奖赏下降过程中,nac - gpe通路的激活对舔舐没有明显的影响,而nac - gpi或nac - vp通路的激活则引起了显著的完满抑制。在没有蔗糖降速的情况下,暴露于2%蔗糖(实验2)或32%蔗糖(实验3)的动物,nac - gpi和nac - vp途径的化学发生激活也产生了更高的终性抑制。这些影响并没有伴随着空地运动功能障碍的证据,也没有明显的趋势表明蔗糖的适口性下降,特别是在2%蔗糖和水之间的选择。然而,初步观察表明,CNO注射后的舔舐抑制也增强了调节箱在获得32%蔗糖和相对于载体注射时的活性。因此,这些BG通路以不同的方式调节完善行为,但BG功能障碍是否影响对意外奖励下降的行为反应仍有待确定。
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引用次数: 0
The interval between conditional stimulus onset and unconditional stimulus onset, not training-to-test interval, determines patterns of immediate early gene expression in the anterior retrosplenial cortex 条件刺激开始和无条件刺激开始之间的时间间隔,而不是训练到测试的时间间隔,决定了脾前后皮层的即时早期基因表达模式
IF 2.2 4区 心理学 Q3 BEHAVIORAL SCIENCES Pub Date : 2025-06-18 DOI: 10.1016/j.nlm.2025.108074
Sydney Trask , Jaden B. Brooks , Sean Warner
Prior work has found that the retrosplenial cortex (RSC) is necessary for formation and retrieval of trace, but not delay, fear conditioning. However, more recently, others have demonstrated that activity in the retrosplenial cortex is necessary for retrieval of a remotely-acquired delay fear memory, suggesting that as memory undergoes systems consolidation it becomes more dependent on neural activity in the RSC. Here, we aimed to examine expression of the immediate early gene zif268 in two distinct subregions of the retrosplenial cortex (anterior and posterior) following retrieval of either a recently-acquired or remotely-acquired delay fear memory. We found that while presenting the conditional stimulus either 1 day or 30 days following delay fear conditioning produced strong conditional responding, activity in either the anterior or posterior RSC assessed through expression of the immediate early gene zif268 was not elevated in the remote retrieval group, contrary to our hypothesis. Instead, activity in the pRSC was elevated in the group that received conditioning the day before. In line with some of our prior work, this suggests that animals in that group were showing neural activity in response to placement in a novel context. We then aimed to determine the circumstances under which delay fear retrieval could produce changes in the anterior RSC, which has been associated with conditional stimulus (CS) encoding and retrieval in a trace fear paradigm. We therefore compared delay and trace conditions to a delay conditioning procedure in which the CS and unconditional stimulus (US) onsets were matched to that of the trace procedure. We found that while both the trace and long-cue delay groups showed a similar behavioral pattern, with freezing that gradually extinguished throughout the 10-CS session, freezing in the standard delay group remained high. When examining zif268 activity, we found that while all three groups showed elevated zif268 expression in the pRSC, only the long-cue delay and trace groups showed increased aRSC activity. Interestingly, only the short-cue delay group showed increased zif268 activity in the basolateral amygdala, corresponding with their elevated fear behavior throughout the session. Together, these results suggest that zif268 activity in the RSC following conditioning is related to the interval between CS onset and US onset.
先前的研究发现,脾后皮层(RSC)是形成和恢复痕量恐惧条件反射所必需的,而不是延迟恐惧条件反射。然而,最近,其他人已经证明,脾后皮层的活动对于远程获得的延迟恐惧记忆的检索是必要的,这表明随着记忆经历系统巩固,它变得更加依赖于RSC的神经活动。在这里,我们的目的是在最近获得的或远程获得的延迟恐惧记忆恢复后,检测直接早期基因zif268在两个不同的脾后皮层亚区(前部和后部)的表达。我们发现,当延迟恐惧条件反射后1天或30天呈现条件刺激时,会产生强烈的条件反应,通过即时早期基因zif268的表达评估,在远程检索组中,前部或后部RSC的活性均未升高,这与我们的假设相反。相反,在前一天接受条件反射的组中,pRSC的活性升高。与我们之前的一些工作一致,这表明那组动物在对新环境的反应中表现出神经活动。然后,我们旨在确定延迟恐惧检索在何种情况下会产生与条件刺激(CS)编码和检索相关的前侧RSC的变化。因此,我们将延迟条件和跟踪条件与延迟条件过程进行了比较,其中CS和无条件刺激(US)的开始与跟踪过程的开始相匹配。我们发现,虽然线索延迟组和长线索延迟组都表现出类似的行为模式,在10-CS会话中,冻结逐渐消失,但标准延迟组的冻结仍然很高。当检测zif268活性时,我们发现虽然所有三组在pRSC中的zif268表达均升高,但只有长线索延迟组和微量组的aRSC活性升高。有趣的是,只有短提示延迟组显示出杏仁核基底外侧的zif268活性增加,这与他们在整个过程中升高的恐惧行为相对应。总之,这些结果表明,条件反射后RSC中zif268的活性与CS发病和US发病之间的间隔有关。
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引用次数: 0
The REM effect: How sleep stages influence learning strategies in complex reward-based decision-making 快速眼动效应:睡眠阶段如何影响基于奖励的复杂决策中的学习策略。
IF 2.2 4区 心理学 Q3 BEHAVIORAL SCIENCES Pub Date : 2025-06-12 DOI: 10.1016/j.nlm.2025.108072
Eleni Kavaliotis , Justin Mahlberg , Daniel Bennett , Antonio Verdejo-García , Rowan P. Ogeil , Sean P.A. Drummond
Model-free (MF) and model-based (MB) learning strategies are complementary decision-making processes used in evaluating choices with potential rewards. Disorders involving compulsive behaviours (e.g., substance use, gambling) are suggested to emerge from an overreliance on MF learning, though the reasons for this bias remain unclear. Sleep disruptions, common in these disorders, could be a contributing factor, however no study has examined the impact of sleep and/or sleep loss on an individual’s engagement of each strategy. Thus, this study examined the influence of sleep on MF/MB learning in healthy adults. Participants (n = 67, Mage = 26.21yrs, SD = 5.82yrs, females = 65.67%) completed a two-stage reinforcement learning paradigm following a week of either sleep restriction (5-hr time in bed/night) or well-rested sleep (9-hr/night). Using mixed-effect logistic regressions and comprehensive computational modelling, we found no differences in MF and MB learning based on sleep condition (all p = > 0.05). However, regressions showed less REM sleep was associated with increased use of MB learning, whilst greater levels of REM sleep were associated with increased use of MF learning. Computational modelling supported this, revealing negative associations between the MB parameter estimate and REM sleep percentage (τ = -0.22, p = 0.02). This suggests the amount of REM sleep prior to learning may potentially play a role in determining which strategy will dominate. In particular, individuals with less REM sleep may be less willing or able to assess the relative costs and benefits of each strategy. Future research should explore this relationship further.
无模型(MF)和基于模型(MB)的学习策略是互补的决策过程,用于评估具有潜在回报的选择。强迫性行为(例如,药物使用,赌博)的障碍被认为是过度依赖MF学习的结果,尽管这种偏见的原因尚不清楚。在这些疾病中常见的睡眠中断可能是一个促成因素,但没有研究调查睡眠和/或睡眠不足对个人参与每种策略的影响。因此,本研究考察了睡眠对健康成人MF/MB学习的影响。参与者(n = 67,男 = 26.21yrs, SD = 5.82yrs,女性 = 65.67 %)在一周的睡眠限制(每晚5小时的床上时间)或充分休息的睡眠(每晚9小时)后完成了两阶段的强化学习范式。使用混合效应逻辑回归和综合计算模型,我们发现基于睡眠状态的MF和MB学习没有差异(p = > 0.05)。然而,回归结果显示,快速眼动睡眠时间越短,脑动神经学习的使用越多,而快速眼动睡眠时间越长,脑动神经学习的使用越多。计算模型支持这一点,揭示了MB参数估计与REM睡眠百分比之间的负相关(τ = -0.22,p = 0.02)。这表明,学习前的快速眼动睡眠时间可能在决定哪种学习策略占主导地位方面发挥着潜在的作用。特别是,快速眼动睡眠较少的人可能不太愿意或无法评估每种策略的相对成本和收益。未来的研究应进一步探讨这种关系。
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Neurobiology of Learning and Memory
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