Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by early sensorimotor delays, which often precede core social deficits as well as restricted and repetitive behaviors. Environmental enrichment (EE) is a promising behavioral intervention for ASD; however, its potential to prevent these earliest neurodevelopmental disruptions remains unexplored. This study investigated whether sustained EE could prevent early milestone delays in a prenatal valproic acid (VPA) rat model of ASD. Female Wistar rats were housed in standard (SH) or EE conditions for eight weeks, beginning two weeks before conception and continuing through lactation. Dams received a single injection of VPA (500 mg/kg) or saline on gestational day 12.5. Offspring were assessed daily from postnatal day (PND) 1–21 for the acquisition of physical and sensorimotor milestones. EE significantly mitigated VPA-induced delays in a subset of key neurodevelopmental milestones. While EE did not fully normalize development to control levels, a composite neurodevelopmental score revealed that EE significantly attenuated the global impairment induced by VPA. These findings demonstrate that preconception-perinatal EE confers partial protection against functional neurodevelopmental deficits in a predictive ASD model, highlighting its potential as a preventive strategy targeting the earliest manifestations of neurodevelopmental disruption.
{"title":"Environmental enrichment partially rescues neurodevelopmental milestone delays in the prenatal VPA rat model of autism spectrum disorders","authors":"Oussama Duieb, Ayoub Rezqaoui, Soufiane Boumlah, Laila Ibouzine-Dine, Hasnaa Mallouk, Soumia Ed-Day, Aboubaker Elhessni, Abdelhalem Mesfioui","doi":"10.1016/j.bbr.2025.116003","DOIUrl":"10.1016/j.bbr.2025.116003","url":null,"abstract":"<div><div>Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by early sensorimotor delays, which often precede core social deficits as well as restricted and repetitive behaviors. Environmental enrichment (EE) is a promising behavioral intervention for ASD; however, its potential to prevent these earliest neurodevelopmental disruptions remains unexplored. This study investigated whether sustained EE could prevent early milestone delays in a prenatal valproic acid (VPA) rat model of ASD. Female Wistar rats were housed in standard (SH) or EE conditions for eight weeks, beginning two weeks before conception and continuing through lactation. Dams received a single injection of VPA (500 mg/kg) or saline on gestational day 12.5. Offspring were assessed daily from postnatal day (PND) 1–21 for the acquisition of physical and sensorimotor milestones. EE significantly mitigated VPA-induced delays in a subset of key neurodevelopmental milestones. While EE did not fully normalize development to control levels, a composite neurodevelopmental score revealed that EE significantly attenuated the global impairment induced by VPA. These findings demonstrate that preconception-perinatal EE confers partial protection against functional neurodevelopmental deficits in a predictive ASD model, highlighting its potential as a preventive strategy targeting the earliest manifestations of neurodevelopmental disruption.</div></div>","PeriodicalId":8823,"journal":{"name":"Behavioural Brain Research","volume":"500 ","pages":"Article 116003"},"PeriodicalIF":2.3,"publicationDate":"2025-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145797739","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Chronic social stress is a major risk for psychopathologies such as depression, often leading to altered hypothalamic-pituitary-adrenal (HPA) axis function and glucocorticoid resistance. This study examines how chronic social defeat stress (CSDS) affects sensitivity to dexamethasone by analyzing HPA axis genes expression in C57Bl/6 mice. Adult male mice were subjected to 30 days of stress, followed by dexamethasone or saline administration. Genes expression was analyzed in the hypothalamus, prefrontal cortex (PFC; Nr3c1 only), and adrenal glands at multiple time points post-treatment. CSDS induced marked dysregulation of HPA axis-related genes, including a decrease in hypothalamic Crh and Crhbp, and adrenal Mc2r, Nr3c1, alongside an upregulation of steroidogenic enzymes Cyp11a1 and Cyp11b1, which may account for the elevated corticosterone levels observed under chronic stress conditions. CSDS alters the genes expression response to dexamethasone, indicating a delayed recovery of glucocorticoid receptor signaling in the brain and adrenal glands. Our findings reveal significant stress-induced alterations in the expression of key HPA axis genes, suggesting impaired glucocorticoid receptor signaling and potential glucocorticoid resistance in stressed mice.
{"title":"The effect of chronic stress on sensitivity to dexamethasone treatment of HPA axis gene expression in C57Bl/6 mice","authors":"Rasha Salman , Polina Ritter , Yuliya Ryabushkina , Julia Khantakova , Natalya Bondar","doi":"10.1016/j.bbr.2025.116000","DOIUrl":"10.1016/j.bbr.2025.116000","url":null,"abstract":"<div><div>Chronic social stress is a major risk for psychopathologies such as depression, often leading to altered hypothalamic-pituitary-adrenal (HPA) axis function and glucocorticoid resistance. This study examines how chronic social defeat stress (CSDS) affects sensitivity to dexamethasone by analyzing HPA axis genes expression in C57Bl/6 mice. Adult male mice were subjected to 30 days of stress, followed by dexamethasone or saline administration. Genes expression was analyzed in the hypothalamus, prefrontal cortex (PFC; <em>Nr3c1</em> only), and adrenal glands at multiple time points post-treatment. CSDS induced marked dysregulation of HPA axis-related genes, including a decrease in hypothalamic <em>Crh</em> and <em>Crhbp</em>, and adrenal <em>Mc2r, Nr3c1</em>, alongside an upregulation of steroidogenic enzymes <em>Cyp11a1</em> and <em>Cyp11b1</em>, which may account for the elevated corticosterone levels observed under chronic stress conditions. CSDS alters the genes expression response to dexamethasone, indicating a delayed recovery of glucocorticoid receptor signaling in the brain and adrenal glands. Our findings reveal significant stress-induced alterations in the expression of key HPA axis genes, suggesting impaired glucocorticoid receptor signaling and potential glucocorticoid resistance in stressed mice.</div></div>","PeriodicalId":8823,"journal":{"name":"Behavioural Brain Research","volume":"500 ","pages":"Article 116000"},"PeriodicalIF":2.3,"publicationDate":"2025-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145780107","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Inferring agency—the experience of controlling one’s own actions and their consequences—often relies on integrating cues from multiple sources, and recent studies have highlighted the importance of considering the temporal dynamics of this integration process. While previous research has examined how the presence or absence of agency (i.e., reliable versus unreliable sensorimotor cues) affects the neural processing of action-outcomes, it remains unclear whether sensorimotor cues influence this processing dynamically or statically, and how these neural changes relate to explicit judgments of agency. In the present study, participants performed a task in which they moved a ball to a target position under varying motion fluency conditions and then received social feedback regarding their performance, followed by an agency judgement task. Electroencephalography was recorded to capture neural responses during feedback processing. Analyses revealed a dynamic interaction between motion fluency and feedback valence on both the feedback-related negativity (FRN) and explicit agency ratings. Under disfluent motion, the influence of social feedback on both neural responses and agency ratings intensified over time. In contrast, under fluent motion, the influence of social feedback diminished over time. Additionally, FRN was associated with the integration of fluency and feedback, whereas the later P3 component was primarily associated with the influence of fluency on agency ratings. These results indicated that the reflective agency during outcome monitoring could involve an early integration and later differentiation of cues, with the early phase integrating both the sensorimotor and external cues, and the later phase focusing on a more in-depth processing of sensorimotor cues.
{"title":"Inferring agency: A two-stage process from early integration to late differentiation during action-outcome monitoring","authors":"Yunyun Chen , Xintong Zou , Jianxin Zhao , Xuemin Zhang","doi":"10.1016/j.bbr.2025.115999","DOIUrl":"10.1016/j.bbr.2025.115999","url":null,"abstract":"<div><div>Inferring agency—the experience of controlling one’s own actions and their consequences—often relies on integrating cues from multiple sources, and recent studies have highlighted the importance of considering the temporal dynamics of this integration process. While previous research has examined how the presence or absence of agency (i.e., reliable versus unreliable sensorimotor cues) affects the neural processing of action-outcomes, it remains unclear whether sensorimotor cues influence this processing dynamically or statically, and how these neural changes relate to explicit judgments of agency. In the present study, participants performed a task in which they moved a ball to a target position under varying motion fluency conditions and then received social feedback regarding their performance, followed by an agency judgement task. Electroencephalography was recorded to capture neural responses during feedback processing. Analyses revealed a dynamic interaction between motion fluency and feedback valence on both the feedback-related negativity (FRN) and explicit agency ratings. Under disfluent motion, the influence of social feedback on both neural responses and agency ratings intensified over time. In contrast, under fluent motion, the influence of social feedback diminished over time. Additionally, FRN was associated with the integration of fluency and feedback, whereas the later P3 component was primarily associated with the influence of fluency on agency ratings. These results indicated that the reflective agency during outcome monitoring could involve an early integration and later differentiation of cues, with the early phase integrating both the sensorimotor and external cues, and the later phase focusing on a more in-depth processing of sensorimotor cues.</div></div>","PeriodicalId":8823,"journal":{"name":"Behavioural Brain Research","volume":"500 ","pages":"Article 115999"},"PeriodicalIF":2.3,"publicationDate":"2025-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145767028","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-14DOI: 10.1016/j.bbr.2025.115998
Elif Aksoz , Medine Karabulut , Mustafa Hilmi Yaranoğlu
Aim
Dietary intake and synthesis of vitamin D synthesis decline with age, increasing the risk of vitamin D deficiency. Dementia and Alzheimer's disease development are closely linked to vitamin D deficiency. In this study, we investigated whether vitamin D supplementation could attenuate age-related effects on memory and the hippocampal cholinergic system in aged rats.
Method
Thirty Wistar albino male rats (young: 4–5 months old, aged: 21–22 months old) were included in this study. Animals were divided into three groups: The Young control and the Aged control groups were administered physiological serum and the Aged + Vitamin D group was administered vitamin D (500 IU/kg/day). Spatial memory was assessed with the Morris Water Maze test. Then, ACh level and ChAT, AChE, and BChE enzyme activities in the hippocampus were examined.
Results
Vitamin D supplementation given to aged rats increased the AchE and BuChE enzyme activities and ACh levels which decreased with aging. The activity of the ChAT enzyme did not change in the aged group, and vitamin D supplementation did not affect it. Increased hippocampal cholinergic transmission improved the spatial memory of aged rats in the MWM test.
Conclusion
Vitamin D supplementation improved spatial memory in rats, probably by reversing the aging-related changes in brain cholinergic functions. Vitamin D shows promise in delaying cognitive decline associated with aging and AD.
{"title":"Vitamin D3 supplementation reverses aging-related changes in cholinergic functions and improves spatial memory in aged rats","authors":"Elif Aksoz , Medine Karabulut , Mustafa Hilmi Yaranoğlu","doi":"10.1016/j.bbr.2025.115998","DOIUrl":"10.1016/j.bbr.2025.115998","url":null,"abstract":"<div><h3>Aim</h3><div>Dietary intake and synthesis of vitamin D synthesis decline with age, increasing the risk of vitamin D deficiency. Dementia and Alzheimer's disease development are closely linked to vitamin D deficiency. In this study, we investigated whether vitamin D supplementation could attenuate age-related effects on memory and the hippocampal cholinergic system in aged rats.</div></div><div><h3>Method</h3><div>Thirty Wistar albino male rats (young: 4–5 months old, aged: 21–22 months old) were included in this study. Animals were divided into three groups: The Young control and the Aged control groups were administered physiological serum and the Aged + Vitamin D group was administered vitamin D (500 IU/kg/day). Spatial memory was assessed with the Morris Water Maze test. Then, ACh level and ChAT, AChE, and BChE enzyme activities in the hippocampus were examined.</div></div><div><h3>Results</h3><div>Vitamin D supplementation given to aged rats increased the AchE and BuChE enzyme activities and ACh levels which decreased with aging. The activity of the ChAT enzyme did not change in the aged group, and vitamin D supplementation did not affect it. Increased hippocampal cholinergic transmission improved the spatial memory of aged rats in the MWM test.</div></div><div><h3>Conclusion</h3><div>Vitamin D supplementation improved spatial memory in rats, probably by reversing the aging-related changes in brain cholinergic functions. Vitamin D shows promise in delaying cognitive decline associated with aging and AD.</div></div>","PeriodicalId":8823,"journal":{"name":"Behavioural Brain Research","volume":"500 ","pages":"Article 115998"},"PeriodicalIF":2.3,"publicationDate":"2025-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145767103","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-13DOI: 10.1016/j.bbr.2025.115995
Xuting Wang , Xue Wang , Chuncheng Zhao , Haoyu Zhao , Pingping Wang , Tao Song
Alzheimer's disease (AD) imposes a heavy burden on families and society. Rhythmic magnetic stimulation has emerged as a promising non-invasive therapy to mitigate AD-related cognitive decline. In this study, we applied a rhythmic unipolar compound pulsed magnetic field (cPMF; carrier frequency: 40 Hz, repetition rate: 5 Hz, magnetic flux density: 0–20 mT) incorporating both theta and gamma rhythms to evaluate its effects on behavior and neural oscillations in AD mice and to explore the underlying mechanisms. 5xFAD mice received unipolar cPMF stimulation for 1 h/d over 8 consecutive weeks. Learning and memory were assessed using the novel object recognition (NOR) and the Morris water maze (MWM) tests. In NOR test, unipolar cPMF-treated mice showed a higher cognitive index in test phase 2, and in MWM test, exhibited shorter escape latencies in the training trial and spent less time to first cross the precise former platform location with a higher crossing frequency over this target area in the probe trial. Local field potentials (LFPs) in the hippocampal CA1 area were recorded via in vivo electrophysiology. LFP analysis showed that unipolar cPMF treatment enhanced power of cognitive-related neural oscillations and strengthened theta-gamma phase-amplitude coupling. RNA sequencing analysis further indicated that unipolar cPMF-treated mice exhibited differential gene expression in molecular function and multiple neurotransmitter synaptic signaling pathways. In conclusion, unipolar cPMF might improve cognitive function in 5xFAD mice by modulating cognitive-related neural oscillations. These findings could provide experimental support for the low-intensity pulsed magnetic stimulation as a potential therapeutic strategy for AD.
{"title":"Enhancement of cognitive behavior and hippocampal neural oscillations by rhythmic unipolar pulsed magnetic stimulation in 5xFAD Alzheimer's disease mice","authors":"Xuting Wang , Xue Wang , Chuncheng Zhao , Haoyu Zhao , Pingping Wang , Tao Song","doi":"10.1016/j.bbr.2025.115995","DOIUrl":"10.1016/j.bbr.2025.115995","url":null,"abstract":"<div><div>Alzheimer's disease (AD) imposes a heavy burden on families and society. Rhythmic magnetic stimulation has emerged as a promising non-invasive therapy to mitigate AD-related cognitive decline. In this study, we applied a rhythmic unipolar compound pulsed magnetic field (cPMF; carrier frequency: 40 Hz, repetition rate: 5 Hz, magnetic flux density: 0–20 mT) incorporating both theta and gamma rhythms to evaluate its effects on behavior and neural oscillations in AD mice and to explore the underlying mechanisms. 5xFAD mice received unipolar cPMF stimulation for 1 h/d over 8 consecutive weeks. Learning and memory were assessed using the novel object recognition (NOR) and the Morris water maze (MWM) tests. In NOR test, unipolar cPMF-treated mice showed a higher cognitive index in test phase 2, and in MWM test, exhibited shorter escape latencies in the training trial and spent less time to first cross the precise former platform location with a higher crossing frequency over this target area in the probe trial. Local field potentials (LFPs) in the hippocampal CA1 area were recorded via <em>in vivo</em> electrophysiology. LFP analysis showed that unipolar cPMF treatment enhanced power of cognitive-related neural oscillations and strengthened theta-gamma phase-amplitude coupling. RNA sequencing analysis further indicated that unipolar cPMF-treated mice exhibited differential gene expression in molecular function and multiple neurotransmitter synaptic signaling pathways. In conclusion, unipolar cPMF might improve cognitive function in 5xFAD mice by modulating cognitive-related neural oscillations. These findings could provide experimental support for the low-intensity pulsed magnetic stimulation as a potential therapeutic strategy for AD.</div></div>","PeriodicalId":8823,"journal":{"name":"Behavioural Brain Research","volume":"500 ","pages":"Article 115995"},"PeriodicalIF":2.3,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145761986","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The Self-Determination Theory posits that extrinsic reward withdrawal often undermines intrinsic motivation. This undermining effect varies according to the reward category (e.g., monetary vs. praise). However, the mechanism underlying this variability remains unclear, partly because previous studies have conceptualized intrinsic motivation as a single construct without distinguishing liking (intrinsic value) from wanting (motivational drive). Failure to make this distinction may obscure the effects of rewards on each component. We hypothesized that extrinsic reward withdrawal would differentially affect intrinsic value and motivational drive. To test this hypothesis, we conducted functional magnetic resonance imaging (fMRI) on 54 participants who were randomly assigned to one of three conditions: control (no rewards), monetary reward, or social reward. Participants in the monetary and social reward groups played a stopwatch game twice, first with and then without extrinsic rewards. The control group received no extrinsic rewards during the task. We assessed intrinsic value through fMRI-measured activation of the reward system and motivational drive through voluntary engagement during the task intermission. Intrinsic value, measured by activation in predefined reward-related regions, declined in the control group but was preserved in both extrinsic reward groups after withdrawal. Thus, both monetary and social rewards were associated with preserved intrinsic value. However, intrinsic behavioral motivation declined in the monetary group but was maintained in the social group. These findings suggest that extrinsic reward withdrawal differentially influences intrinsic value and motivational drive across reward categories, thereby clarifying the variability of the undermining effect.
{"title":"Beyond the undermining effect: Extrinsic rewards preserve neural intrinsic reward","authors":"Hiroaki Ayabe , Takahiko Koike , Ayumi Yoshioka , Satoshi Izuno , Kanae Ogasawara , Shohei Tsuchimoto , Norihiro Sadato","doi":"10.1016/j.bbr.2025.115996","DOIUrl":"10.1016/j.bbr.2025.115996","url":null,"abstract":"<div><div>The Self-Determination Theory posits that extrinsic reward withdrawal often undermines intrinsic motivation. This undermining effect varies according to the reward category (e.g., monetary vs. praise). However, the mechanism underlying this variability remains unclear, partly because previous studies have conceptualized intrinsic motivation as a single construct without distinguishing <em>liking</em> (intrinsic value) from <em>wanting</em> (motivational drive). Failure to make this distinction may obscure the effects of rewards on each component. We hypothesized that extrinsic reward withdrawal would differentially affect intrinsic value and motivational drive. To test this hypothesis, we conducted functional magnetic resonance imaging (fMRI) on 54 participants who were randomly assigned to one of three conditions: control (no rewards), monetary reward, or social reward. Participants in the monetary and social reward groups played a stopwatch game twice, first with and then without extrinsic rewards. The control group received no extrinsic rewards during the task. We assessed intrinsic value through fMRI-measured activation of the reward system and motivational drive through voluntary engagement during the task intermission. Intrinsic value, measured by activation in predefined reward-related regions, declined in the control group but was preserved in both extrinsic reward groups after withdrawal. Thus, both monetary and social rewards were associated with preserved intrinsic value. However, intrinsic behavioral motivation declined in the monetary group but was maintained in the social group. These findings suggest that extrinsic reward withdrawal differentially influences intrinsic value and motivational drive across reward categories, thereby clarifying the variability of the undermining effect.</div></div>","PeriodicalId":8823,"journal":{"name":"Behavioural Brain Research","volume":"501 ","pages":"Article 115996"},"PeriodicalIF":2.3,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145762007","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-12DOI: 10.1016/j.bbr.2025.115991
Yuhong Ou , Renlai Zhou
Understanding how individuals with high test anxiety (HTA) process evaluative feedback is essential to clarifying their responses in evaluative situations. This study examined how individuals with HTA differ from those with low test anxiety (LTA) in processing positive and negative outcomes presented in reward and punishment contexts. Using event-related potentials (ERPs) and a probabilistic learning task, we implemented separate reward and punishment blocks with test-related and test-unrelated images.
Behavioral results indicated that, across reward and punishment blocks, both HTA and LTA individuals responded more quickly and accurately as the task progressed, with no significant performance differences between the groups. ERP findings revealed no deficits in reward processing for individuals with HTA. However, during punishment processing, HTA individuals showed smaller feedback-related negativity (FRN) and larger late positive potential (LPP) amplitudes in response to negative feedback for test-related stimuli. They also exhibited larger FRN amplitudes after positive feedback for test-related stimuli, while no significant group differences were observed in P3 or LPP amplitudes. These findings suggest altered neural responses to evaluative feedback in individuals with HTA, particularly under punitive conditions, which may reflect differences in expectancy and emotional engagement.
{"title":"Neurophysiological correlates of reward and punishment feedback processing in individuals with test anxiety","authors":"Yuhong Ou , Renlai Zhou","doi":"10.1016/j.bbr.2025.115991","DOIUrl":"10.1016/j.bbr.2025.115991","url":null,"abstract":"<div><div>Understanding how individuals with high test anxiety (HTA) process evaluative feedback is essential to clarifying their responses in evaluative situations. This study examined how individuals with HTA differ from those with low test anxiety (LTA) in processing positive and negative outcomes presented in reward and punishment contexts. Using event-related potentials (ERPs) and a probabilistic learning task, we implemented separate reward and punishment blocks with test-related and test-unrelated images.</div><div>Behavioral results indicated that, across reward and punishment blocks, both HTA and LTA individuals responded more quickly and accurately as the task progressed, with no significant performance differences between the groups. ERP findings revealed no deficits in reward processing for individuals with HTA. However, during punishment processing, HTA individuals showed smaller feedback-related negativity (FRN) and larger late positive potential (LPP) amplitudes in response to negative feedback for test-related stimuli. They also exhibited larger FRN amplitudes after positive feedback for test-related stimuli, while no significant group differences were observed in P3 or LPP amplitudes. These findings suggest altered neural responses to evaluative feedback in individuals with HTA, particularly under punitive conditions, which may reflect differences in expectancy and emotional engagement.</div></div>","PeriodicalId":8823,"journal":{"name":"Behavioural Brain Research","volume":"500 ","pages":"Article 115991"},"PeriodicalIF":2.3,"publicationDate":"2025-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145755172","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-12DOI: 10.1016/j.bbr.2025.115992
Shuai Jin , Xue Wei , Peihua Xian , Junshu Ma , Shenghao Shi , Zhiyuan Liu
Given the complexity of the environment and the constraints on cognitive resources, missed opportunities frequently arise in risky decision-making. However, the relationship between regret feelings for missed opportunities and subsequent risky decision-making among maximizers, as well as the influence of time pressure on this dynamic, remains unclear. Based on 580 participants, we conducted a cross-sectional survey and two EEG experiments to investigate these issues. The results revealed a positive correlation between maximization and risk-taking tendency (Study 1). Compared to satisficers, maximizers showed stronger regret feelings and increased the late positive potential (LPP) amplitudes in response to missed opportunities, and were more inclined to engage in risky decisions. Moreover, maximizers’ regret feelings about missed opportunities facilitated their risky decision-making by amplifying LPP amplitudes (Study 2). Compared to the low-time-pressure condition, maximizers exhibited diminished regret feelings and reduced LPP amplitudes in response to missed opportunities, and less risky decision-making behavior under the high-time-pressure condition. Additionally, time pressure attenuated the association between regret feelings for missed opportunities and risky decision-making (Study 3). Overall, this study highlights that maximizers’ regret feelings about missed opportunities drive them to take risky decision-making, and time pressure can reduce the degree to which this occurs.
{"title":"Beyond the road not taken: Experienced regret-induced risk seeking in maximizers","authors":"Shuai Jin , Xue Wei , Peihua Xian , Junshu Ma , Shenghao Shi , Zhiyuan Liu","doi":"10.1016/j.bbr.2025.115992","DOIUrl":"10.1016/j.bbr.2025.115992","url":null,"abstract":"<div><div>Given the complexity of the environment and the constraints on cognitive resources, missed opportunities frequently arise in risky decision-making. However, the relationship between regret feelings for missed opportunities and subsequent risky decision-making among maximizers, as well as the influence of time pressure on this dynamic, remains unclear. Based on 580 participants, we conducted a cross-sectional survey and two EEG experiments to investigate these issues. The results revealed a positive correlation between maximization and risk-taking tendency (Study 1). Compared to satisficers, maximizers showed stronger regret feelings and increased the late positive potential (LPP) amplitudes in response to missed opportunities, and were more inclined to engage in risky decisions. Moreover, maximizers’ regret feelings about missed opportunities facilitated their risky decision-making by amplifying LPP amplitudes (Study 2). Compared to the low-time-pressure condition, maximizers exhibited diminished regret feelings and reduced LPP amplitudes in response to missed opportunities, and less risky decision-making behavior under the high-time-pressure condition. Additionally, time pressure attenuated the association between regret feelings for missed opportunities and risky decision-making (Study 3). Overall, this study highlights that maximizers’ regret feelings about missed opportunities drive them to take risky decision-making, and time pressure can reduce the degree to which this occurs.</div></div>","PeriodicalId":8823,"journal":{"name":"Behavioural Brain Research","volume":"500 ","pages":"Article 115992"},"PeriodicalIF":2.3,"publicationDate":"2025-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145755083","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-11DOI: 10.1016/j.bbr.2025.115986
Liu Ning , Ou Yang Yan Ping , Ren Sai Nan
This study explores how cognitive style diversity (differences in information processing among team members) influences group creativity through interpersonal neural mechanisms. 116 college students were assigned to high-diversity (HD) groups (mix of field-independent and field-dependent individuals) or low-diversity (LD) groups (homogeneous cognitive styles). Both groups completed a creative task (umbrella design) and a routine task (desk purchase) while their prefrontal cortex (PFC) and right temporoparietal junction (r-TPJ) activity was monitored via fNIRS. Results revealed that HD groups produced significantly more novel ideas than LD groups. fNIRS data showed enhanced brain synchronization in HD groups within the frontal pole and dorsolateral prefrontal cortex (DLPFC). Field-independent individuals dominated neural interactions in HD groups, with delayed inter-brain synchronization positively correlating with creative novelty. Findings suggest cognitive diversity fosters group creativity through complementary neural coordination between field-independent and field-dependent individuals.
{"title":"Cognitive styles diversity and group creativity: Evidence from fNIRS hyperscanning","authors":"Liu Ning , Ou Yang Yan Ping , Ren Sai Nan","doi":"10.1016/j.bbr.2025.115986","DOIUrl":"10.1016/j.bbr.2025.115986","url":null,"abstract":"<div><div>This study explores how cognitive style diversity (differences in information processing among team members) influences group creativity through interpersonal neural mechanisms. 116 college students were assigned to high-diversity (HD) groups (mix of field-independent and field-dependent individuals) or low-diversity (LD) groups (homogeneous cognitive styles). Both groups completed a creative task (umbrella design) and a routine task (desk purchase) while their prefrontal cortex (PFC) and right temporoparietal junction (r-TPJ) activity was monitored via fNIRS. Results revealed that HD groups produced significantly more novel ideas than LD groups. fNIRS data showed enhanced brain synchronization in HD groups within the frontal pole and dorsolateral prefrontal cortex (DLPFC). Field-independent individuals dominated neural interactions in HD groups, with delayed inter-brain synchronization positively correlating with creative novelty. Findings suggest cognitive diversity fosters group creativity through complementary neural coordination between field-independent and field-dependent individuals.</div></div>","PeriodicalId":8823,"journal":{"name":"Behavioural Brain Research","volume":"500 ","pages":"Article 115986"},"PeriodicalIF":2.3,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145740688","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-11DOI: 10.1016/j.bbr.2025.115994
Hongchi Zhang , Amir Jahanian-Najafabadi , Khaled Bagh , Lorenza Colzato , Bernhard Hommel
Previous research has linked psychiatric disorders to alterations in the aperiodic exponent—a measure of excitatory–inhibitory (E/I) balance derived from resting-state EEG that reflects broadband, non-oscillatory brain activity. This measure also appears sensitive to age-related neurodevelopmental changes. In this study, we investigated whether the aperiodic exponent varies with age in children and adolescents diagnosed with adjustment disorder (AD) or oppositional defiant disorder (ODD), compared to age-matched healthy controls. While healthy participants showed no significant association between age and the aperiodic exponent, both clinical groups exhibited a pronounced nonlinear relationship. Specifically, the exponent was lower in early childhood and early adulthood, but peaked around 9–10 years of age. This U-shaped developmental trajectory suggests a deviation from normative brain maturation in AD and ODD and points to temporally specific alterations in cortical E/I balance. These findings underscore the potential of the aperiodic exponent as a developmentally sensitive neural marker of externalising psychopathology and may inform age-tailored diagnostic and intervention strategies in child and adolescent psychiatry.
{"title":"Tracking the developing brain: Resting-state aperiodic activity reveals nonlinear cortical maturation in externalizing disorders","authors":"Hongchi Zhang , Amir Jahanian-Najafabadi , Khaled Bagh , Lorenza Colzato , Bernhard Hommel","doi":"10.1016/j.bbr.2025.115994","DOIUrl":"10.1016/j.bbr.2025.115994","url":null,"abstract":"<div><div>Previous research has linked psychiatric disorders to alterations in the aperiodic exponent—a measure of excitatory–inhibitory (E/I) balance derived from resting-state EEG that reflects broadband, non-oscillatory brain activity. This measure also appears sensitive to age-related neurodevelopmental changes. In this study, we investigated whether the aperiodic exponent varies with age in children and adolescents diagnosed with adjustment disorder (AD) or oppositional defiant disorder (ODD), compared to age-matched healthy controls. While healthy participants showed no significant association between age and the aperiodic exponent, both clinical groups exhibited a pronounced nonlinear relationship. Specifically, the exponent was lower in early childhood and early adulthood, but peaked around 9–10 years of age. This U-shaped developmental trajectory suggests a deviation from normative brain maturation in AD and ODD and points to temporally specific alterations in cortical E/I balance. These findings underscore the potential of the aperiodic exponent as a developmentally sensitive neural marker of externalising psychopathology and may inform age-tailored diagnostic and intervention strategies in child and adolescent psychiatry.</div></div>","PeriodicalId":8823,"journal":{"name":"Behavioural Brain Research","volume":"500 ","pages":"Article 115994"},"PeriodicalIF":2.3,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145740728","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}