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Hepatic encephalopathy (HE) is a neuropsychiatric syndrome with a wide spectrum of cognitive deficits, motor impairment, and psychiatric disturbances resulting from liver damage. The cytokine TNF has been considered the main cytokine in the development and progression of HE, with a pivotal role in the initiation and amplification of the inflammatory cascade. The aim of the present study was to evaluate the involvement of TNF type 1 receptor (TNFR1) in locomotor deficits and in the levels of TNF, IFN-γ, IL-6, IL-10, IL-12p70, CCL2, CX3CL1 and BDNF from the frontal cortex and hippocampus of TNFR1 knockout mice (TNFR1-/-) mice with HE induced by thioacetamide. Wild-type (WT) animals with HE developed locomotor deficit. The absence of TNFR1 absence of TNFR1 in HE animals attenuated the locomotor activity impairment in parallel with a balanced neuroinflammatory environment 24 h after the administration of thioacetamide. Taken together, the data suggests that the absence of TNFR1 promoted a protective response in the early phase of hepatic encephalopathy induced by thioacetamide in mice. [ABSTRACT FROM AUTHOR]

[Display omitted] Prenatal stress increases the risk of neurodevelopmental disorders. NMDA-type glutamate receptor (NMDAR) activity plays an important pathophysiological role in the cortico-hippocampal circuit in these disorders. We tested the hypothesis that transcription of NMDAR subunits is modified in the frontal cortex (FCx) and hippocampus after exposure to prenatal restraint stress (PRS) in mice. At 10 weeks of age, male PRS offspring (n = 20) and non-stressed controls (NS, n = 20) were treated with haloperidol (1 mg/kg), clozapine (5 mg/kg) or saline twice daily for 5 days, before measuring social approach (SOC). Saline-treated and haloperidol-treated PRS mice had reduced SOC relative to NS (P < 0.01), but clozapine-treated PRS mice had similar SOC to NS mice. These effects of PRS were associated with increased transcription of NMDAR subunits encoded by GRIN2A and GRIN2B genes in the hippocampus but not FCx. GRIN transcription in FCx correlated positively with SOC, but hippocampal GRIN transcription had negative correlation with SOC. The ratio of GRIN2A/GRIN2B transcription is known to increase during development but was lower in PRS mice. These results suggest that GRIN2A and GRIN2B transcript levels are modified in the hippocampus by PRS, leading to life-long deficits in social behavior. These data have some overlap with the molecular pathophysiology of schizophrenia. Similar to PRS in mice, schizophrenia, has been associated with social withdrawal, with increased GRIN2 expression in the hippocampus, and reduced GRIN2A/GRIN2B expression ratios in the hippocampus. These findings suggest that PRS in mice may have construct validity as a preclinical model for antipsychotic drug development. [ABSTRACT FROM AUTHOR]

Brain-derived neurotrophic factor (BDNF), a member of the neurotrophin family, plays key roles in neuronal protection and synaptic plasticity. Changes in BDNF are associated with various pathological conditions, including methamphetamine (meth) addiction, although the effects of meth on BDNF expression are not always consistent. We have previously demonstrated region-specific effects of a chronic meth regime on BDNF methylation and expression in the rat brain. This study aims to determine the effect of chronic meth administration on the expression of BDNF protein using immunohistochemistry in the rat frontal cortex and hippocampus. Novel object recognition (NOR) as a measure of cognitive function was also determined. Male Sprague Dawley rats were administered a chronic escalating dose (0.1–4 mg/kg over 14 days) (ED) of meth or vehicle; a subgroup of animals receiving meth were also given an acute "binge" (4x6mg) dose on the final day before NOR testing. The results showed that hippocampal CA1 BDNF protein was significantly increased by 72 % above control values in the ED-binge rats, while other hippocampal regions and frontal cortex were not significantly affected. Meth-administered animals also demonstrated deficits in NOR after 24 h delay. No significant effect of the additional binge dose on BDNF protein or NOR findings was apparent. This finding is consistent with our previous results of reduced DNA methylation and increased expression of the BDNF gene in this region. The hippocampal BDNF increase may reflect an initial increase in a protective factor produced in response to elevated glutamate release resulting in neurodegenerative excitotoxicity. [ABSTRACT FROM AUTHOR]

• The frequent use of caffeinated products and food preservatives influence CNS. • Caffeine group boosted exploratory activity as well as anxiolytic effect. • Caffeine + SB 400 persuaded histological changes in frontal cortex and hippocampus. • Undesirable working memory consequences was detected by caffeine + SB 400. • The frequent use of fast food and energy drinks during adolescence is warned. The continuous high intake of caffeinated products may harm CNS. Sodium benzoate (SB), broadly used for food preservation, may also have an impact. The current research studied the influence of caffeine and two doses of SB during adolescence period on behavior and brain alterations. Adolescent rats (90–120 gm) were exposed to vehicle, SB 100 and 400 mg/kg, p.o, caffeine (30 mg/kg, i.p), SB 100 or 400 + caffeine for 28 days. Locomotor performances were assessed by the open field, learning and memory were considered with novel object and y-maze, while anxiety was evaluated by light and dark as well as successive allays tests. The results showed that the motor activity of adolescent rats increased with each single treatment. Recognition memory was improved by SB 100 and its combination with caffeine while working memory was reduced by SB (100 or 400) combination with caffeine compared with caffeine group. The anxiolytic effect of caffeine was reduced by SB co-treatment in either dose. Concerning biochemical study in the frontal cortex and hippocampus, oxidative biomarkers as well as Cholinesterase content were elevated due to SB 400 + caffeine. Dopamine content was almost elevated by all treatments in both regions while GABA content was increased in the frontal cortex only. The obtained results pointed to histopathological changes as a result of brain oxidative stress and undesirable working memory consequences due to caffeine administration with SB, mostly the large dose. The outcomes propose new recommendations to evade the consolidation between processed nourishment and caffeinated beverages during adolescence. [ABSTRACT FROM AUTHOR]

• We investigated cortical activity and game performance in first-person shooter (FPS) players in similar to actual gaming environments. • High-skilled FPS players have fast reaction times and high accuracy during tasks. • High-skilled FPS players had a lower delta and theta power spectral density in the frontal and temporal areas. • High cortical activity and accuracy during the task were associated. First-person shooting (FPS) games are among the most famous video games worldwide. However, cortical activities in environments related to real FPS games have not been studied. This study aimed to determine differences in cortical activity between low- and high-skilled FPS game players using 160-channel electroencephalography. Nine high-skilled FPS game players (official ranks: above the top 10%) and eight low-skilled FPS game players (official ranks: lower than the top 20%) were recruited for the experiment. The task was set for five different conditions using the AimLab program, which was used for the FPS game players' training. Additionally, we recorded the brain activity in the resting condition before and after the task, in which the participants closed their eyes and relaxed. The reaction time and accuracy (the number of hit-and-miss targets) were calculated to evaluate the task performance. The results showed that high-skilled FPS game players have fast reaction times and high accuracy during tasks. High-skilled FPS game players had higher cortical activity in the frontal cortex than low-skilled FPS game players during each task. In low-skilled players, cortical activity level and performance level were associated. These results suggest that high cortical activity levels were critical to achieving high performance in FPS games. [ABSTRACT FROM AUTHOR]

Highlights • iTBS stimulation in the DLPFC decreases cortical excitability in the M1. • cTBS stimulation in the DLPFC increases cortical excitability in the M1. • There is bi-direction change of excitability from the stimulated DLPFC to the M1. Abstract Background The human motor system consists of several divisions in the frontal lobes. The physiological function of projections from the dorsolateral prefrontal cortex (DLPFC) to the primary motor cortex (M1) remains elusive. Here, we introduce theta burst stimulation (TBS)-based protocols to target inhibitory and facilitatory connections in the DLPFC-M1 network. Methods Intermittent and continuous TBS with 600 pulses (iTBS600/cTBS600) were applied to the left DLPFC. Resting motor threshold (RMT), motor-evoked potential (MEP), and short-interval intracortical inhibition (SICI) were measured with transcranial magnetic stimulation to the ipsilateral M1. Results iTBS600 to the DLPFC decreased MEP amplitude in M1. Conversely, cTBS600 to the DLPFC increased MEP amplitude in M1. The peak decrease in MEP amplitude after iTBS600 was negatively correlated with the peak increase in MEP amplitude after cTBS600. There were no significant effects in the control group with the sham stimulation. Discussion These results provide insight into the regulation of inhibitory and facilitatory balance from the local DLPFC to M1. TBS modulation in one brain region will induce interactions within other remote cortical areas. Our results enable better understanding of how cognitive resources are allocated to achieve optimal control of motor output. [ABSTRACT FROM AUTHOR]

In the applications of the graph theory, it is unusual that one considers numerous, pairwise different graphs on the very same set of vertices. In the case of human braingraphs or connectomes, however, this is the standard situation: the nodes correspond to anatomically identified cerebral regions, and two vertices are connected by an edge if a diffusion MRI-based workflow identifies a fiber of axons, running between the two regions, corresponding to the two vertices. Therefore, if we examine the braingraphs of n subjects, then we have n graphs on the very same, anatomically identified vertex set. It is a natural idea to describe the k -frequently appearing edges in these graphs: the edges that are present between the same two vertices in at least k out of the n graphs. Based on the NIH-funded large Human Connectome Project's public data release, we have reported the construction of the Budapest Reference Connectome Server http://www.connectome.pitgroup.org that generates and visualizes these k -frequently appearing edges. We call the graphs of the k -frequently appearing edges “ k -consensus connectomes” since an edge could be included only if it is present in at least k graphs out of n . Considering the whole human brain, we have reported a surprising property of these consensus connectomes earlier. In the present work we are focusing on the frontal lobe of the brain, and we report here a similarly surprising dynamical property of the consensus connectomes when k is gradually changed from k  =  n to k  = 1: the connections between the nodes of the frontal lobe are seemingly emanating from those nodes that were connected to sub-cortical structures of the dorsal striatum: the caudate nucleus, and the putamen. We hypothesize that this dynamic behavior copies the axonal fiber development of the frontal lobe. An animation of the phenomenon is presented at https://youtu.be/wBciB2eW6_8 . [ABSTRACT FROM AUTHOR]

• The brain is modality-independent in processing higher-order linguistic information. • Information flow aggregation in low-frequency-responsive primary sensory cortex. • The information flow with high frequency response is characterized by bottom-up. • The information flow dominated by low and high frequency presents a top-down feature. Neural oscillations subserve a broad range of speech processing and language comprehension functions. Using an electroencephalogram (EEG), we investigated the frequency-specific directed interactions between whole-brain regions while the participants processed Chinese sentences using different modality stimuli (i.e., auditory, visual, and audio-visual). The results indicate that low-frequency responses correspond to the process of information flow aggregation in primary sensory cortices in different modalities. Information flow dominated by high-frequency responses exhibited characteristics of bottom-up flow from left posterior temporal to left frontal regions. The network pattern of top-down information flowing out of the left frontal lobe was presented by the joint dominance of low- and high-frequency rhythms. Overall, our results suggest that the brain may be modality-independent when processing higher-order language information. [ABSTRACT FROM AUTHOR]

• Select tau species and other neuronal proteins are detected in the submandibular gland of human cases. • The evaluated neuronal proteins experience differential protein levels based on anatomic region (submandibular gland or frontal cortex) and clinicopathological stage of AD. • Tissues innervated by the peripheral nervous system may experience unique selective vulnerabilities in AD. Hyperphosphorylation of the microtubule-associated protein tau is hypothesized to lead to the development of neurofibrillary tangles in select brain regions during normal aging and in Alzheimer disease (AD). The distribution of neurofibrillary tangles is staged by its involvement starting in the transentorhinal regions of the brain and in final stages progress to neocortices. However, it has also been determined neurofibrillary tangles can extend into the spinal cord and select tau species are found in peripheral tissues and this may be depended on AD disease stage. To further understand the relationships of peripheral tissues to AD, we utilized biochemical methods to evaluate protein levels of total tau and phosphorylated tau (p-tau) as well as other neuronal proteins (i.e., tyrosine hydroxylase (TH), neurofilament heavy chain (NF-H), and microtubule-associated protein 2 (MAP2)) in the submandibular gland and frontal cortex of human cases across different clinicopathological stages of AD (n = 3 criteria not met or low, n = 6 intermediate, and n = 9 high likelihood that dementia is due to AD based on National Institute on Aging-Reagan criteria). We report differential protein levels based on the stage of AD, anatomic specific tau species, as well as differences in TH and NF-H. In addition, exploratory findings were made of the high molecular weight tau species big tau that is unique to peripheral tissues. Although sample sizes were small, these findings are, to our knowledge, the first comparison of these specific protein changes in these tissues. [ABSTRACT FROM AUTHOR]

Introduction Multiple components of the dystrophin-associated protein complex (DAPC) are expressed in numerous tissues including the brain. Members of the DAPC and dysbindin are abnormally expressed in the brain of Duchenne Muscular Dystrophy (DMD) patients, which has been associated with cognitive impairments. However, little is known about the expression pattern of individual members of the DAPC in animal models of DMD and their relationship with dysbindin. Methods Ten mdx mice were randomly allocated into a control and intervention group [(−)-epicatechin (Epi) 1 mg/kg/day for four weeks] and results compared to a wild-type mice. After sacrifice, brain pre-frontal cortices were collected for Western blotting and immunoprecipitation assays, and sagittal sections processed for immunohistochemistry. Results Epi promotes a partial recovery of DAPC members [α1-Syntrophin, sarcoglycans (SG), dystrophin 71 (Dp71)], dysbindin, and utrophin protein levels. Epi also appears to restore the association of DAPC between dysbindin, and utrophin with Dp71 and ε-SG. Co-immunostaining evidence increased protein levels of dysbindin, dystrophin, and ε-SG and their colocalization. Conclusions Altogether, results suggest that Epi is capable of restoring pre-frontal cortex DAPC and dysbindin levels of mdx mice towards that of healthy brains. The functional implications of such studies warrant further investigation. [ABSTRACT FROM AUTHOR]

• How insufficient sleep affects cognitive function has not been clear. • CSR could induce the decrease of circulating IGF-1 in mice. • Down-regulating IGF-1R could reduce Aβ deposition via inhibiting BACE-1 after CSR. • Inhibiting IGF-1 pathway might be a protection mechanism for alleviating CSR. Insufficient sleep affects cognitive function, but the underlying mechanism and potential protective ways are yet to be fully understood. This study aimed to explore the influence of chronic sleep restriction (CSR) on the insulin-like growth factor-1 (IGF-1) signaling pathway, and whether down-regulating IGF-1 signaling pathway would modulate amyloid-β (Aβ) peptides metabolism and its cortical deposition after CSR. Methods 8-week IGF-1R+/- mice and wild-type (WT) C57BL/6 (C57) mice were divided into four groups: IGF-1R+/- CSR (MUSR), IGF-1R+/- control (MUCO), C57 CSR (C57SR) and C57 control (C57CO). CSR model was established by application of slowly rotating drum for 2 months. Body weight and Lee's index were measured. The level of IGF-1 in plasma was measured by enzyme linked immunosorbent assay (ELISA). Aβ accumulation was detected by immunofluorescence. The expressions of amyloid precursor protein (APP), β-site amyloid precursor protein-cleaving enzyme-1 (BACE-1) and C99 were detected using western-blot (WB). Results Two-way ANOVA showed genotypic effect was significant on body weight and Lee's index. Neither treatment effect nor interaction reached significant difference on body weight and Lee's index. The level of IGF-1 in plasma was significantly decreased in C57SR compared with C57CO. Besides, compared with C57CO, Aβ was markedly accumulated in frontal cortex, in parallel with increased expressions of BACE-1 and C99, and with no difference of APP in C57SR group. Further, no significant changes of Aβ, BACE-1, C99 and APP were detected in MUSR compared with MUCO. Conclusions This study showed that CSR could induce the decrease of circulating IGF-1 in mice. By using the IGF-1R+/- mice, we found that down-regulating IGF-1R could reduce Aβ deposition in mice frontal cortex after CSR via inhibiting BACE-1 protein expression and activity, which were independent of the changes of body weight and Lee's index. These findings indicate that the blockage of IGF-1 signaling pathway might be a protection mechanism for alleviating the impact of CSR. [ABSTRACT FROM AUTHOR]

• MSTA and HSTA groups had similar damage in bilateral CST and Left SLT fiber. • MSTA patients had worse ATR and IFOT diffusion than HSTA patients. • Fusiform and superior temporal gyrus cortical thickness was consistently damaged. • Mismatched aberrant gray matter lesions were extensive in two groups. Heroin and methamphetamine cause great damage to individuals and society. However, numerous withdrawal mechanisms remain unidentified. In this study, 19 heroin short-term abstinent (HSTA) patients, 20 methamphetamine short-term abstinent (MSTA) patients, and 27 healthy controls (HCs) were scanned using multimodal magnetic resonance imaging. Degraded nodes of fiber tracts were identified using automated fiber quantification. Voxel- and surface-based morphometric measurements were performed to determine the gray matter volume and cortical thickness. The MSTA and HSTA groups had abnormal diffusion metrics in a variety of bilateral corticospinal tract (CST) and left superior longitudinal tract (SLT) nodes compared with the HC group. The MSTA patients reported more severely disrupted diffusion metrics in certain nodes of the bilateral anterior thalamic radiation and left inferior fronto-occipital tract than the HSTA patients. The MSTA and HSTA groups exhibited identical cortical damage in the fusiform and superior temporal gyri, as well as in the superior frontal gyrus, posterior cerebellum, and precentral gyrus. Extensive differences in gray matter lesions were observed between the MSTA and HSTA groups. Neuroimaging mechanisms of short-term abstinence may aid in the development of rehabilitation strategies. [ABSTRACT FROM AUTHOR]

• Pain associated with bottom-up activation from Ventral Attention System. • Task demand increased top-down activation on frontoparietal network. • Top-down activation increased when pain combined with high task demand. • Right inferior frontal gyrus implicated as hub for interhemispheric connectivity. The dorsal and ventral attention networks (DAN & VAN) provide a framework for studying attentional modulation of pain. It has been argued that cognitive demand distracts attention from painful stimuli via top-down reinforcement of task goals (DAN), whereas pain exerts an interruptive effect on cognitive performance via bottom-up pathways (VAN). The current study explores this explanatory framework by manipulating pain and task demand in combination with functional near-infrared spectroscopy (fNIRS) and Granger Causal Connectivity Analyses (GCCA). Twenty-one participants played a racing game at low and high difficulty levels with or without experimental pain (administered via a cold pressor test). Six channels of fNIRS were collected from bilateral frontal eye fields and intraparietal sulci (DAN), with right-lateralised channels at the inferior frontal gyrus and temporoparietal junction (VAN). Our first analysis revealed increased G-causality from bottom-up pathways (VAN) during the cold pressor test. However, an equivalent experience of experimental pain during gameplay increased G-causality in top-down (DAN) pathways, with the left intraparietal sulcus serving a hub of connectivity. High game difficulty increased G-causality via top-down pathways and implicated the right inferior frontal gyrus as an interhemispheric hub. Our results are discussed with reference to existing models of both networks and attentional modulation of pain. [ABSTRACT FROM AUTHOR]

It is a point of controversy as to whether directed forgetting effects are a result of active inhibition or a change of context initiated by the instruction to forget. In this study we test the causal role of active inhibition in directed forgetting. By applying cathodal transcranial direct current stimulation (tDCS) over the right prefrontal cortex we suppressed cortical activity commonly associated with inhibitory control. Participants who underwent real brain stimulation before completing the directed forgetting paradigm showed no directed forgetting effects. Conversely, those who underwent sham brain stimulation demonstrated classical directed forgetting effects. We argue that these findings suggest that inhibition is the primary mechanism that results in directed forgetting costs and benefits. [ABSTRACT FROM AUTHOR]

This study investigated whether catechol- O -methyltransferase (COMT) Val/Met polymorphism was associated with variation in event-related desynchronization/synchronization (ERD/ERS) of responses during working memory (WM). 11 Val/Val and 11 Met/Met homozygous participants underwent magnetoencephalography (MEG) while performing a WM task. In contrast to small effects behaviourally, during the delay period Val/Val individuals showed lower ERS in the gamma band (Hz 30–50) in frontal regions, increased ERS in the alpha band (Hz 8–12) in the right frontal and parietal regions and increased ERD in the beta band (Hz 14–30) in the left fronto-temporal regions as compared with Met/Met homozygous individuals. During the response period Val/Val participants showed greater beta ERD in the prefrontal and parietotemporal regions. These results demonstrate that COMT genotype has a strong impact on brain responses (oscillatory activity) during WM performance likely a consequence of compensatory activity during the delay and response periods. [ABSTRACT FROM AUTHOR]

[Display omitted] • The COVID-19 pandemic of Shanghai 2022 has led many young adults to stay indoors. • It's the first fNIRS study on long-term effects of confinement and music stimulation. • The negative emotions increased significantly with the length of confinement. • Negative emotions may inhibit prefrontal function in young people. • Music stimulation improve efficiency by altering the pattern of connections in frontal lobe. The Corona Virus Disease 2019 (COVID-19) pandemic may have had a negative emotional impact on individuals. This study investigated the effect of long-term lockdown and music on young people's mood and neurophysiological responses in the prefrontal cortex (PFC). Fifteen healthy young adults were recruited and PFC activation was acquired using functional near-infrared spectroscopy during the conditions of resting, Stroop and music stimulation. The Depression Anxiety Stress Scales mental scale scores were simultaneously recorded. Mixed effect models, paired t-tests, one-way ANOVAs and Spearman analyses were adopted to analyse the experimental parameters. Stress, anxiety and depression levels increased significantly from Day 30 to Day 40. In terms of reaction time, both Stroop1 and Stroop2 were faster on Day 40 than on Day 30 (P = 0.01, P = 0.003). The relative concentration changes of oxyhemoglobin were significantly higher during premusic conditions than music stimulation and postmusic Stroop. The intensity of functional connectivity shifted from inter- to intracerebral over time. In conclusion, the reduced hemodynamic response of the PFC in healthy young adults is associated with negative emotions, especially anxiety, during lockdown. Immediate music stimulation appears to improve efficiency by altering the pattern of connections in PFC. [ABSTRACT FROM AUTHOR]

• Functional connectivity (FC) of firefighters with low sleep quality was explored. • Poor sleepers had weaker FC centred on attentional network seeds. • Sleep duration was associated with FC centred on the ventral frontal cortex. [ABSTRACT FROM AUTHOR]

This study assessed whether the use of an “anchor system” benefited older adults who performed a tandem walking task. Additionally, we tested the effects of practice with the anchor system during walking on trunk stability, in the frontal plane, of older adults. Forty-four older adults were randomly assigned to three groups: control group, 0 g anchor group, and 125 g anchor group. Individuals in each group performed a tandem walking task on the GaitRite system with an accelerometer placed on the cervical region. The participants in the 125 g anchor group held, in each hand, a flexible cable with a light mass attached at the end of the cable, which rested on the ground. While the participants walked, they pulled on the cables just enough to keep them taut as the masses slid over the ground. The 0 g anchor group held an anchor tool without any mass attached to the end portion. The results of this study demonstrated that the use of the anchor system contributed to the reduction of trunk acceleration in the frontal plane. However, this effect did not persist after removal of the anchors, which suggests that the amount of practice with this tool was insufficient to generate any lasting effect, or that the task was not sufficiently challenging, or both. [ABSTRACT FROM AUTHOR]

Previous in vitro binding studies identified a 7-fluoro derivative of marsanidine, a partial α 2 -adrenoceptor (α 2 -AR) agonist, to display high affinity and selectivity for α 2 -AR over α 1 -AR, imidazoline-1 and imidazoline-2 binding sites. In the present study 7-fluoro-marsanidine is further characterised in vivo to investigate its pharmacological effects on extracellular noradrenaline (NA) levels at frontal cortex in conscious freely moving rats using the technique of in vivo brain microdialysis. Peripheral administration of 7-fluoro-marsanidine via intraperitoneal (i.p.) route at the dose of 0.1 mg/kg slightly, but non-significantly, decreased extracellular NA level (maximum by 17% at 20 min) in rat frontal cortex compared to basal level. At a higher dose of 1 mg/kg, 7-fluoro-marsanidine reduced cortical NA level (maximum by 73% at 40 min) significantly as compared to basal level between 20 and 80 min. In addition, systemic administration of 7-fluoro-marsanidine at both the doses produced rapid onset of sedation in rats. These data suggest that 7-fluoro-marsanidine is able to cross the blood–brain barrier and, by acting as an α 2 -AR agonist, reduces extracellular NA levels in rat frontal cortex in a dose related manner. Thus, initial studies indicate 7-fluoro-marsanidine to possess favourable functional properties at α 2 -AR. [ABSTRACT FROM AUTHOR]

Highlights: [•] Using fMRI, we investigated the neural basis of made-up face processing. [•] The OFC showed greater activity for made-up faces than for faces without make-up. [•] OFC activity reflected increasing facial attractiveness by cosmetics use. [•] We show a direct link between the OFC and enhanced attractiveness of made-up faces. [ABSTRACT FROM AUTHOR]

[Display omitted] • EtOH 3.0 g/kg dose increased the levels of DOPAC and HVA and decreased the levels of 3-MT. • Clorgyline alone increased 3-MT and decreased DOPAC and HVA levels. • Tolcapone alone increased DOPAC and decreased 3-MT and HVA levels. • Combination of EtOH with clorgyline or tolcapone further decreased 3-MT and increased DOPAC and HVA levels. First, we aimed to investigate ex vivo the effects of ethanol (EtOH) on levels of norepinephrine (NE), dopamine (DA), serotonin (5-HT), and their metabolites in the frontal cortex, hippocampus, and striatum of Aldh2 -knockout (Aldh2 -KO) and wild-type (WT) mice. Animals were treated intraperitoneally with saline (control) or EtOH (1.0, 2.0, or 3.0 g/kg). Brain samples were collected 60 and 120 min after EtOH injection, and monoamines and their metabolites were measured by HPLC-ECD. We found in both WT and Aldh2 -KO mice that 3.0 g/kg EtOH increased the levels of 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) and decreased the level of 3-methoxytyramine (3-MT). A 2.0 g / kg dose of EtOH also increased HVA, but there was not a consistent effect within the brain regions of Aldh2 -KO and WT mice. There were inconsistent findings of genotype differences in the levels of DA, 5-HT, and their metabolites in the brain regions tested. None of the EtOH doses altered NE, DA, 5-HT, or 5-hydroxyindoleacetic acid contents in any of the brain regions studied. Second, we tested whether EtOH-induced increases in DOPAC and HVA are mediated by increased monoamine oxidase (MAO) or catechol-O-methyltransferase (COMT) activity. To test this, we used the MAO blocker clorgyline (2.0 and 4.0 mg/kg) and the COMT blocker tolcapone (15 and 30 mg/kg) alone or in combination with EtOH (3.0 g/kg). Clorgyline alone increased 3-MT and decreased DOPAC and HVA levels, whereas tolcapone alone increased DOPAC and decreased 3-MT and HVA levels. Surprisingly, the combination of EtOH with clorgyline (4.0 mg/kg) or tolcapone (30 mg/kg) further decreased 3-MT and increased DOPAC and HVA levels, an effect that reversed the inhibitor-induced decreases in HVA. These results suggest that a high concentration of EtOH can accelerate DA metabolism, as evidenced by the increase in DOPAC and HVA, and this effect is likely a consequence of increased degradation of DA by MAO. [ABSTRACT FROM AUTHOR]

• 7,8-DHF does not modify drinking in IA2BC paradigm. • 7,8-DHF has weak effect on anxiety-like behavior during early abstinence after IA2BC. • 7,8-DHF enhances SHH in a region-specific manner during early abstinence. A mimetic of brain-derived neurotrophic factor (BDNF), 7,8-dihydroxyflavone (7,8-DHF), alleviates some aspects of alcohol abstinence after voluntary alcohol intake in rodents. The interaction between BDNF and sonic hedgehog (SHH) was demonstrated in adult brain in some situations, though relationship between BDNF and SHH during alcohol abstinence remains obscure. We aimed to study effect of 7,8-DHF on drinking pattern, anxiety-like behavior and expression of SHH and a downstream transcription factor, GLI, in the limbic brain structures during early abstinence after voluntary ethanol intake. Male Wistar rats were subjected to intermittent access to 20% ethanol in a two-bottle choice procedure (IA2BC). The animals experienced twenty 24-h sessions of free access to two-bottle choice (water or 20% ethanol) with 24-h withdrawal periods (water only); 7,8-DHF (5 mg/kg, i.p.) was administered one hour prior to each alcohol access session. Anxiety-like behavior was estimated in the open-field (OFT) and elevated plus-maze (EPM) tests on the first and second days of abstinence, respectively. The expression of SHH and GLI was analyzed on the third day after withdrawal in the frontal cortex, hippocampus and striatum. Repeated measures ANOVA did not show significant main effect of 7,8-DHF injections during IA2BC on ethanol intake and ethanol preference over water. As expected, pair-wise comparisons of OFT and EPM data by Mann-Whitney U test revealed elevated anxiety-like behavior during early abstinence in IA2BC paradigm as compared with control group. When all groups were included in the analysis, Kruskal-Wallis ANOVA did not show significant differences in time spent in the center zone of the OFT and number of entries. However, time spent in the open arms of the EPM but not number of entries differed significantly between the groups studied according to Kruskal-Wallis ANOVA. Factorial ANOVA followed by Tukey's HSD post hoc test demonstrated significant elevation of SHH protein levels in the hippocampus and striatum but not in the frontal cortex of animals with access to ethanol and administered with 7,8-DHF as compared with respective animals without 7,8-DHF. GLI expression changed only in the hippocampus; its protein level increased in control animals administered 7,8-DHF. Thus, 7,8-DHF administration during IA2BC procedure induces region-specific levels elevation of SHH in the brain, but does not significantly change drinking pattern and anxiety-like behavior during early abstinence. [ABSTRACT FROM AUTHOR]

Highlights: [•] Rats were exposed to oral nicotine choice starting at adolescence or adulthood. [•] Brain nitrate+nitrite determined in rats with maximum/minimum nicotine preference. [•] Control rats received only water from both bottles, naïve rats were group housed. [•] Isolation stress increased NO metabolites in the hippocampus (naïve–control). [•] Preference had no effect; adolescent-onset rats had higher NO activity in frontal cortex. [ABSTRACT FROM AUTHOR]

Abstract: Mirror neurons are a class of neurons in the ventral pre-motor cortex (area F5) and inferior parietal lobule (area PFG) that respond during the execution as well as the observation of goal-directed motor acts. These intriguing response properties stirred an intense debate in the scientific community with respect to the possible cognitive role of mirror neurons. The aim of the present review is to contribute to this debate by providing, in a single paper, an extended summary of 20 years of neurophysiological research on mirror neurons in the macaque. To this end, I provide a comprehensive description of the methodology and the main results of each paper about mirror neurons published since their first report in 1992. Particular care was devoted in reporting the different response characteristics and the percentages of neurons exhibiting them in relation to the total number of studied neurons. Furthermore, I also discuss recent results indicating that mirror neurons might not be confined to areas F5 and PFG and that “mirroring” might not be limited to action observation. Finally, I offer a unifying framework for many of the results discussed here by speculating that a potential functional role of mirror neurons might be, during action observation, to generalize from the particular grasping movement being observed to the “concept” of grasping. [Copyright &y& Elsevier]

Abstract: Psychophysiological detection of deception has seen increased attention in both research and applied settings. In this field, the most scientifically validated paradigm is the Concealed Information Test (CIT). The CIT does not directly deal with whether a participant is lying, but examines whether a participant recognizes a critical relevant detail, inferred by differences in physiological responses between critical and non-critical items. Although event-related potential (ERP) approaches to the CIT have shown high accuracy, a combination of measures might improve the test''s performance. We thus assessed whether a new CIT index, frontal EEG asymmetry that is supposed to reflect differences in approach/withdrawal motivation, would prove useful. Nineteen participants were asked to steal one item in a mock crime, and were then administered two CITs while concealing the stolen item. One CIT included the stolen item (i.e., guilty condition), whereas the other CIT did not (i.e., innocent condition). In the guilty condition, the concealed stolen item elicited greater relative left frontal alpha activity (indicative of relative right frontal cortical activity) as compared to the other items, suggesting that the recognition of the concealed item might have induced withdrawal motivation. Although the discrimination between guilty and innocent conditions by the asymmetry score alone was not as good as that by the ERP P3 index, combining the asymmetry score and P3 improved the detection performance significantly. The results suggest that the frontal EEG asymmetry can be used as a new measure in the CIT that provides additional information beyond that captured by the traditional ERP index. [Copyright &y& Elsevier]

Abstract: Previous event-related potentials (ERPs) research has suggested that the retrieval tasks for many sources of items were operated in the frontal regions, but Cycowicz et al. [2–4,6] recorded the late posterior negativity (LPN), a component over the posterior cortex, in retrieving the associative color sources of pictures. To examine whether the LPN could also be observed in retrieving both the associative and the organizational color sources of verbal stimuli, two experiments were designed by using Chinese nouns as stimuli. Both experiments revealed significant LPN that was related to the tasks of color source retrieval. These findings demonstrate that the association between LPN and search for and/or retrieval/evaluation of the colors of objects is fairly strong, and this association is insensitive to both the attributes of stimulus materials and those of the color sources. [Copyright &y& Elsevier]

Abstract: Recently, research on attention has focused on 3 networks that are linked to separate brain regions, i.e. orienting, alerting, and executive control. The attention network test (ANT) is one of the methods to measure the three attention functions. However, neuropsychological investigations have not examined the anatomical disassociation of different attention networks with the same task. We compared the efficiencies of the 3 networks between brain-damaged patients (27 frontal lesions, 20 temporal lesions, and 21 parietal lesions) and healthy controls (N =58) with ANT. Comparing the brain damaged group with the normal controls, a reduced efficiency of the executive network was found in patients with frontal lobe and parietal lobe injuries, and there was also a deficit in the orienting network in patients with parietal lobe injuries. Analysis of lateralization indicated the right hemisphere superiority to the alerting system. The present study found that the three attentional networks were selectively impaired following brain damage which affected different areas in the brain. [Copyright &y& Elsevier]

Abstract: It is well-known that physical exercise can affect cognition and the frontal lobe is an important structure involved in motor function and cognition. Furthermore, many functional neuroimaging studies have demonstrated that cortical activation patterns of hand and leg movements differ. However, no study has been undertaken to identify differences between the frontal activation patterns generated by hand and leg movements. In the present study, the frontal activation patterns associated with finger and toe movements, as visualized by functional MRI, were investigated and compared. Twelve healthy volunteers were recruited. Functional MRI was performed using a 1.5T Philips Gyroscan Intera. Flexion-extension movements of fingers or toes were performed in one extremity. Regions of interest (ROIs) were set at the primary sensory-motor cortex (SM1: Brodmann area [BA] 1, 2, 3, 4), the premotor area (PMA: BA 6), and the prefrontal cortex (PFC: BA 8, 9, 10, 11, 46). In SM1, finger movements (10,809) induced more activation than toe movements (5349). On the other hand, in the PMA and PFC, toe movements (PMA: 4201, PFC: 921) induced more activation than finger movements (PMA: 2887, PFC: 912) respectively. In the analysis of relative voxel counts in the PMA and PFC versus the SM1, toe movements generated more activation in the PMA and PFC than finger movements. The PMA and PFC were more activated by toe than finger movements, although the SM1 was more activated by finger movements. [Copyright &y& Elsevier]

Abstract: This study aimed to affirm the use of functional near-infrared spectroscopy (fNIR) in examining frontal lobe role during automatic (i.e., requires retrieval from long-term memory) and method-based (i.e., requires calculation) arithmetic processing. Adult university students (math difficulties [MD] and control) performed simple arithmetic calculations while monitored using an fNIR system designed to image regions within the frontal cortices. Addition and subtraction problems presented on a computer screen belonged to one of three categories: triples “under 10” (e.g., 2+3=?, 5−3=?), triples that “break 10” (e.g., 5+8=?, 13−5=?), or triples “including 10” (e.g., 10+7=?, 17−10=?). fNIR recordings indicated significant interactions between type of triple, operation, and group over left frontal lobe, and between type of triple and group over right frontal lobe. Within-group differences among controls were found in the “break 10” triples with higher DeOxyHb level recorded during subtraction processing. Between-group differences were found in the “break 10” and “including 10” triples for subtraction with higher levels of DeOxyHb recorded among controls. Results imply that among adults frontal lobe is still involved during simple mathematical processing and fNIR recordings can differentiate its role in adults of varying mathematical ability. [Copyright &y& Elsevier]

Abstract: The amyloid β (Aβ) protein is believed to be the key pathological mediator of Alzheimer''s disease (AD) which is the first and most well known type of dementia. Despite a growing body of evidence indicating that Aβ neurotoxicity induces changes in synaptic function, little effort, if any, has been made to investigate the effect of in vivo Aβ treatment on intrinsic neuronal properties. The present study was designed to examine the effects that in vivo Aβ treatment have on the intrinsic repetitive firing properties of CA1 pyramidal neurons, using whole cell patch clamp recording. Protective effect of cannabinoid CB1 receptor activation was also investigated against Aβ-induced alterations in evoked electrophysiological activities. The findings from present study demonstrated that a bilateral injection of Aβ into the prefrontal cortex causes robust changes in activity-dependent electrophysiological responses in hippocampal CA1 pyramidal neurons. The effects of Aβ treatment alone was almost completely prevented by combined treatment with Aβ and ACEA, a selective CB1 receptor agonist. It can be concluded Aβ treatment reduces evoked neuronal activity and activation of CB1 cannabinoid receptors may have beneficial preventative effects on Aβ-induced electrophysiological changes. [Copyright &y& Elsevier]

Abstract: Abnormal baseline brain functional connectivity in attention-deficit/hyperactivity disorder (ADHD) has been revealed in a number of studies by using resting-state functional MRI (rfMRI). The aim of this study was to investigate the spontaneous frontal activities in medication-naïve ADHD boys using the rfMRI derived index, amplitude of low-frequency fluctuation (ALFF). In total 17 ADHD boys and 17 matched controls were recruited to undergo rfMRI scan on a 3.0T MRI system. For each subject, six oblique slices covering the frontal areas were acquired with a rapid sampling rate (TR=400ms). Functional images were processed in AFNI for calculation of ALFF and then group comparison was performed using voxel-based t-test. With a corrected threshold of p <0.05 determined by AlphaSim, we found that in comparison with controls, ADHD patients demonstrated higher ALFF values in the left superior frontal gyrus and sensorimotor cortex (SMC), and lower ALFF values in the bilateral anterior, middle cingulate and the right middle frontal gyrus (MFG). Significant correlations were found between patients’ WSCT measures and the peak ALFF located in the right MFG (r =0.69, p =0.02), and the left SMC (r =0.65, p =0.03). Our results revealed abnormal frontal activities at resting state associated with underlying physiopathology of ADHD, and suggested the ALFF analysis to be a potential approach in further exploration of this disorder. [Copyright &y& Elsevier]

Abstract: There is growing interest in the effects of experience on the neural processes linking action execution and action perception. We tested whether experience with unfamiliar actions can alter desynchronization of alpha-range power in the EEG upon re-observation of those actions. In a training session, participants (N =21) watched videos of novel drawing movements. Half of the movements were imitated after each viewing, and half of the movements were seen but not imitated, thus forming two training conditions: visual plus motor experience (V+M), and visual experience only (VO). In a testing session the next day, participants were shown the same videos of both sets of movements, and were also shown a third, completely novel, set of movements. Imitative performance was better for both training conditions than for novel actions. Event-related EEG desynchronization in the upper alpha band during action observation differed between conditions at frontal electrode sites, with novel actions being associated with less frontal desynchronization compared to V+M and VO actions. Differences between conditions were not noted over other regions. This suggests that moderate amounts of initial experience with novel actions can alter the neural processing of these actions when viewed again, particularly over frontal regions. [Copyright &y& Elsevier]

Abstract: Intrinsic brain activity known as default-mode networks (DMNs) has been observed predominantly within the medial/superior frontal areas, anterior/posterior cingulate gyri, and precuneus using blood-oxygenation-level-dependent (BOLD) functional MRI (fMRI). Despite anecdotal evidence of distinct spatial patterns reflecting neuropsychiatric conditions in these DMNs, rigorous analysis of the characteristic traits of DMNs has been limited in previous studies. In this letter, the reproducibility and potential variability of the anterior and posterior DMNs were evaluated based on individual-level variations in effect sizes, activated areas, and causal interactions. Our results indicated that the DMNs were indeed reproducible between sessions/subjects. Region-specific traits were also observed: the posterior DMN seemed more robust to individual-level variations than the anterior DMN. The proposed analytical methods and reported findings may be useful in the development of a wide range of applications, including those involving clinical populations, which utilize the characteristic traits of DMNs. [Copyright &y& Elsevier]

Abstract: It has recently been reported that prestimulus electroencephalogram (EEG) frontal theta and occipital alpha oscillations of healthy controls were modulated by the type of upcoming tasks, reflecting prestimulus top-down preparation. The present study explored the differences in dynamics of frontal theta and occipital alpha activities between obsessive-compulsive disorder (OCD) patients and healthy participants in terms of reflection of prestimulus top-down regulation. EEGs were recorded from 16 OCD patients and 16 healthy controls using a color and a shape discrimination task. The power and time course of oscillatory activity were calculated by convolving the EEG signals with Morlet wavelets. Although OCD patients yielded significantly lower total alpha and total theta power results than the normal controls, they demonstrated that significantly higher total alpha and total theta power preceded the difficult task (shape-task) as compared to the easy task (color-task). Furthermore, the frontal region, where OCD patients usually revealed abnormalities, showed significant differences in the prestimulus total theta power between the normal and OCD groups. Taken together, frontal theta and occipital alpha oscillations seem to be potent electrophysiological correlates reflecting impairment in the prestimulus top-down processing of OCD patients. [Copyright &y& Elsevier]

Abstract: Occipital transcranial magnetic stimulation applied in a task-free experimental setup leads to enhanced relative negativity of frontally recorded evoked slow potentials under the influence of caffeine (Murd et al., 2010 ). We tested whether this increased negativity could be reversed when a similar magnetic stimulation is applied during quiet sleep where consciousness is absent. Consistently with the hypothesis, non-REM sleep led to relative more positive slow brain potentials, compared to wakefulness. This effect was lateralized to the right hemisphere. We conclude that TMS indeed elicits slow negative potentials in higher arousal states, but the effect has hemispheric specificity depending on how arousal is manipulated. [Copyright &y& Elsevier]

Abstract: Although the mechanisms of visual short term memory (VSTM) are extensively investigated in the recent decade, how we compare the representation stored in VSTM to the perceptual input to detect and process the mismatch information remains largely unclear. The current study explored whether there is an ERP component tracking the mismatch process in VSTM by adopting a delayed matching task. To exclude non-memory factors, for instance, using perceptual representation which dominated in previous studies using this paradigm, we lengthened the blank interval between the two sequentially displayed stimuli to 4s to ensure the first stimuli is stored in VSTM. In order to test the sensitivity of this potential neural index and its functional relation to VSTM comparison process, colored shapes were adopted as materials while both the target feature color and the irrelevant feature shape could be changed. We found both the target feature change and the irrelevant feature change elicited a more negative component N270 (or N2-enhancement) around the anterior areas, with their neural sources located at frontal lobe. These results suggest that the N270 can sensitively reflect the mismatch information between the representation in VSTM and the perceptual input. Moreover, it may reflect the limited-capacity process in the VSTM-perception comparison, in which a deliberative comparison was conducted after an unlimited-capacity comparison process. [Copyright &y& Elsevier]

Abstract: Although different lesion and neuroimaging studies had highlighted the importance of the dorsolateral prefrontal cortex (DLPFC) in language switching, the nature of this higher cortical disorder of communication and its neural correlates have not been clearly established. To further investigate the functional involvement of the DLPFC, we used transcranial magnetic stimulation (TMS) given as theta burst stimulation (TBS) in a bilingual patient showing pathologic language switching after an ischemic stroke involving the left frontal lobe. Inhibitory and excitatory TBS were applied to the left DLPFC, to the right DLPFC, or to an occipital cortical control site. A short-lasting interruption of the pathological language switching occurred after excitatory left DLPFC stimulation, while inhibitory left DLPFC TBS transiently increased the number of utterances produced in the unwanted second language. Effects were non-significant after right DLPFC and occipital TBS. Our findings suggest that left DLPFC is actively involved in language switching. TMS techniques may help in understanding the neural bases of bilingualism. [Copyright &y& Elsevier]

Abstract: Deficient control of irrelevant information with greater age can be demonstrated in paradigms like inhibition of return (IOR). IOR is a mechanism to protect the organism from redirecting attention to a previously scanned irrelevant location and is assumed to be generated slower but to a comparable amount with increasing age. We investigated this putative deficit by means of event-related potentials (ERPs). As expected, IOR developed later in older subjects. In the cue-related ERPs, young subjects showed a large frontocentral N2 (reflecting control or inhibition) which was virtually absent in the old subjects. Instead, the older subjects showed a P3b, reflecting controlled processing of information. Thus, older adults process irrelevant stimuli more like relevant ones, thereby overloading their information processing system. [ABSTRACT FROM AUTHOR]

Abstract: Linkage analysis identified a region on chromosome 9p associated with Frontotemporal Lobar Degeneration (FTLD). A detailed analysis of candidate genes lying in this region demonstrated an association with Ubiquitin Associated Protein (UBAP)1. The distribution of five Single Nucleotide Polymorphisms (SNPs) located in the chromosome 9 haplotype identified via linkage analysis, including UBAP1 rs7018487, UBAP2 rs1785506 and rs307658, and KIF24 rs17350674 and rs10814083, has been determined in a population of 284 patients diagnosed with FTLD, including 245 with behavioural variant Frontotemporal Dementia (bvFTD), 23 with Progressive Aphasia and 16 with Semantic Dementia, compared with 318 age-matched controls. A statistically significant increased frequency of the KIF24 rs17350674 AA genotype was observed in patients compared with controls (7.4 versus 2.5%; P =0.0068, OR: 3.63, CI: 1.58–8.35). Considering each syndrome separately, similar results where obtained in bvFTD versus controls (7.7 versus 2.5%, P =0.005, OR: 3.26, CI: 1.40–7.57). Stratifying for gender, a statistically significant increased genotypic frequency was observed in female patients as compared with female controls (8.9 versus 2.5%, P =0.008, OR: 3.85, CI: 1.36–10.93). In silico analysis predicted that the substitution from W to L caused by the rs17350674 affects protein function (P <0.05). The KIF24 rs17350674 polymorphism likely acts as a risk factor for sporadic FTLD, but a replication study would be needed to confirm these preliminary findings. [ABSTRACT FROM AUTHOR]

Abstract: Respiration is essential for smell perception. Previously we found that 8–12-Hz cortical rhythms were phase-locked to inspiration onset during the presentation of odor stimuli; this is referred to as inspiration phase-locked alpha band oscillation (I-α). Generators of I-α estimated with a dipole fitting model were found in the piriform, the entorhinal cortex (ENT), the amygdala (AMG), the hippocampus (HI) and the orbitofrontal cortex (OFC). Such olfactory perception is said to occur via the orthonasal olfaction route. Another route is the retronasal olfaction route. In this study, we investigated the link between respiration phase and retronasal olfactory perception. Electroencephalograph (EEG) and respiratory flows (separately measured with mouth and nose) were simultaneously recorded during stimulation of subjects’ tongues with liquids of chocolate, sucrose and water. The percentage of subjects correctly identifying the chocolate taste was higher when subjects were asked to breathe through the nose than when they were breathing through the mouth. In the averaged EEGs triggered by the onset of expiration measured from the flow through the nose, a 8–12-Hz oscillation was observed. Generators of this potential were found in the left ENT, HI, AMG and OFC in the order of milliseconds after expiration onset. Perception of retronasal olfaction is dependent on expiration, and combining retronasal olfactory information with gustatory information and somatosensation enable us to identify flavors when drinking and feeding. [Copyright &y& Elsevier]

Abstract: Suicidality is a life-threatening symptom in patients with bipolar disorder (BD). Impulsivity and mood instability are associated with suicidality in mood disorders. Evidence suggests that gray and white matter abnormalities are linked with impulsivity in mood disorders, but little is known about the association between corpus callosum (CC) and impulsivity in BD. We examined the relationship between CC areas, impulsivity and suicidality in BD patients. We studied 10 female BD patients with a history of suicide attempt (mean±SD age 36.2±10.1 years), 10 female BD patients without suicide attempt history (44.2±12.5 years) and 27 female healthy subjects (36.9±13.8 years). Impulsivity was evaluated by the Barratt Impulsivity Scale (BIS). We traced MR images to measure the areas of the CC genu, anterior body, posterior body, isthmus and splenium. The genu was divided into anterior, middle and posterior regions. The suicidal and non-suicidal BD patients had significantly higher BIS total, attention and non-planning scores than the healthy subjects (ps<0.01), and the suicidal BD patients had significantly higher BIS motor scores than the non-suicidal BD and healthy subjects (ps<0.01). There were no significant differences among the three groups on any regional CC areas, although the suicidal BD patients had the smallest areas. The suicidal BD patients showed a significant inverse correlation between anterior genu area and the BIS total (r =−0.75, p =0.04), motor (r =−0.79, p =0.02) and non-planning scores (r =−0.79, p =0.02). These correlations were not found in the non-suicidal BD patients or healthy subjects. The results suggest that the anterior medial frontal region may be involved in the pathophysiology of impulsive and suicidal behaviors in BD. [Copyright &y& Elsevier]