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Social behaviours characterize cooperative, mutualistic, aggressive or parental interactions that occur among conspecifics. Although the Ventral Tegmental Area (VTA) has been identified as a key substrate for social behaviours, the input and output pathways dedicated to specific aspects of conspecific interaction remain understudied. Here, in male mice, we investigated the activity and function of two distinct VTA inputs from superior colliculus (SC-VTA) and medial prefrontal cortex (mPFC-VTA). We observed that SC-VTA neurons display social interaction anticipatory calcium activity, which correlates with orienting responses towards an unfamiliar conspecific. In contrast, mPFC-VTA neuron population activity increases after initiation of the social contact. While protracted phasic stimulation of SC-VTA pathway promotes head/body movements and decreases social interaction, inhibition of this pathway increases social interaction. Here, we found that SC afferents mainly target a subpopulation of dorsolateral striatum (DLS)-projecting VTA dopamine (DA) neurons (VTA DA -DLS). While, VTA DA -DLS pathway stimulation decreases social interaction, VTA DA -Nucleus Accumbens stimulation promotes it. Altogether, these data support a model by which at least two largely anatomically distinct VTA sub-circuits oppositely control distinct aspects of social behaviour. Solié, Contestabile et al. show that the superior colliculus to ventral tegmental area (VTA) pathway encodes orienting behavior toward conspecifics, and modulates VTA dopamine neurons projecting onto dorsolateral striatum perturbing social interaction.

Humans tend to orient their attentional resources towards the same location indicated by spatial signals coming from the others, such as pointing fingers, head turns, or eye-gaze. Here, two experiments investigated whether an attentional orienting response can be elicited even by foot cues. Participants were asked to localize a peripheral target while a task-irrelevant picture of a naked human foot, oriented leftward or rightward, was presented on the centre of the screen. The foot appeared in a neutral posture (i.e., standing upright) or an action-oriented posture (i.e., walking/running). In Experiment 1, neutral and action-oriented feet were presented in two distinct blocks, while in Experiment 2 they were presented intermixed. The results showed that the action-oriented foot, but not the neutral one, elicited an orienting response, though this only emerged in Experiment 2. This work suggests that attentional shifts can be induced by action-oriented foot cues, as long as these stimuli are made contextually salient.

The process of information concealment is more relevant than ever in this day and age. Using a modified concealedinformation test (CIT), we aimed to unmask this process by investigating both the decision and the attempt to conceal information in 38 students. The attempt to conceal (vs. reveal) information induced a differential physiological response pattern within subjects—whereas skin conductance increased in both conditions, respiration and heart rate were suppressed only in the conceal condition—confirming the idea that these measures reflect different underlying mechanisms. The decision to conceal (vs. reveal) information induced enhanced anticipatory skin conductance responses. To our knowledge, this is the first study that observed such anticipatory responses in an informationconcealment paradigm. Together, these findings imply that our physiological responses reflect, to some degree, both the decision and the attempt to conceal information. In addition to strengthening CIT theory, this knowledge sheds novel light on anticipatory responding in decision making.

In the standard Hughson-Westlake hearing tests (Carhart and Jerger 1959), patient responses like a button press, raised hand, or verbal response are used to assess detection of brief test signals such as tones of varying pitch and level. Because of its reliance on voluntary responses, Hughson-Westlake audiometry is not suitable for patients who cannot follow instructions reliably, such as pre-lingual infants (Northern and Downs 2002). As an alternative approach, we explored the use of the pupillary dilation response (PDR), a short-latency component of the orienting response evoked by novel stimuli, as an indicator of sound detection. The pupils of 31 adult participants (median age 24 years) were monitored with an infrared video camera during a standard hearing test in which they indicated by button press whether or not they heard narrowband noises centered at 1, 2, 4, and 8 kHz. Tests were conducted in a quiet, carpeted office. Pupil size was summed over the first 1750 ms after stimulus delivery, excluding later dilations linked to expenditure of cognitive effort (Kahneman and Beatty 1966; Kahneman et al. 1969). The PDR yielded thresholds comparable to the standard test at all center frequencies tested, suggesting that the PDR is as sensitive as traditional methods of assessing detection. We also tested the effects of repeating a stimulus on the habituation of the PDR. Results showed that habituation can be minimized by operating at near-threshold stimulus levels. At sound levels well above threshold, the PDR habituated but could be recovered by changing the frequency or sound level, suggesting that the PDR can also be used to test stimulus discrimination. Given these features, the PDR may be useful as an audiometric tool or as a means of assessing auditory discrimination in those who cannot produce a reliable voluntary response.

The P3a observed after novel events is an event-related potential comprising an early fronto-central phase and a late fronto-parietal phase. It has classically been considered to reflect the attention processing of distracting stimuli. However, novel sounds can lead to behavioral facilitation as much as behavioral distraction. This illustrates the duality of the orienting response which includes both an attentional and an arousal component. Using a paradigm with visual or auditory targets to detect and irrelevant unexpected distracting sounds to ignore, we showed that the facilitation effect by distracting sounds is independent of the target modality and endures more than 1500 ms. These results confirm that the behavioral facilitation observed after distracting sounds is related to an increase in unspecific phasic arousal on top of the attentional capture. Moreover, the amplitude of the early phase of the P3a to distracting sounds positively correlated with subjective arousal ratings, contrary to other event-related potentials. We propose that the fronto-central early phase of the P3a would index the arousing properties of distracting sounds and would be linked to the arousal component of the orienting response. Finally, we discuss the relevance of the P3a as a marker of distraction. •Distracting sounds can either facilitate or impair performance in an unrelated-task.•This facilitation effect is independant of the sensory modality of the target.•This facilitation effect remains stable for at least 1500 ms.•The amplitude of the early-P3 increases with the “arousingness” of the sound.

This study introduces a new experimental method for analyzing auditory signals in the presence of background noise and identifying sounds that are consistently easy for humans to notice in daily environments. Attention to a signal was inferred from a physiological orienting response, measured as the change in heart rate (HR) before and after the presentation of a test sound in an experimental environment designed to simulate daily life. The test sounds consisted of eight musical sounds each composed of two piano notes at different pitches, and eight complex sounds, each composed of two pure tones. Each sound interval—C + E or C + G#—was recorded at four different octaves, covering the frequency range of 130.8 Hz to 1661.4 Hz. The change in HR was calculated as the difference in the mean RR interval (RRI) over five beats before and after the test sound. The strength of the orienting response (OR) was quantified as the RRI difference normalized by the standard deviation of RRI. An absolute value greater than 2 was considered to indicate the presence of an orienting response. Twenty-two healthy young male participants participated in the experiment during a three-day, two-night stay, which was repeated after a washout period of at least one week. The results showed that OR values were reproducible for 11 of the 16 test sounds. Based on the corresponding OR values, C3 + E3 (musical sound) was identified as a suitable pre-signal due to its calming response (negative OR), whereas C6 + G#6 (complex sound) was identified as a suitable alarm signal due to its tension-inducing response (positive OR). These findings suggest that the OR metric for assessing physiological responses, provides a novel and effective approach for objectively evaluating human reactions to unexpected auditory stimuli, when combined with an experimental protocol that simulates daily life and background noise.

Inhibitory control relies on attention, inhibition, and other functions that are integrated across neural networks in an interactive manner. Functional MRI studies have provided excellent spatial mapping of the involved regions. However, finer temporal resolution is needed to capture the underlying neural dynamics and the pattern of their functional contributions. Here, we used anatomically-constrained magnetoencephalography (aMEG) which combines MEG with structural MRI to examine how the spatial (“where”) and temporal (“when”) processing stages and interregional co-oscillations unfold in real time to contribute to inhibitory control. Healthy participants completed a modified Go/NoGo paradigm in which a subset of stimuli was modified to be visually salient (SAL). Compared to the non-modified condition, the SAL manipulation facilitated response withholding on NoGo trials and hindered responding to Go stimuli, reflecting attentional capture effectuated by an orienting response to SAL stimuli. aMEG source estimates indicate SAL stimuli elicited the attentional “circuit breaker” effect through early activity within a right-lateralized network centered around the lateral temporal cortex with additional activity in the pre-supplementary motor area (preSMA) and anterior insula (aINS/FO). Activity of the bilateral inferior frontal cortex responded specifically to inhibitory demands and was generally unaffected by the attentional manipulation. In contrast, early aINS/FO activity was sensitive to stimulus salience while subsequent activity was specific to inhibitory control. Activity estimated to the medial prefrontal cortex including the dorsal anterior cingulate cortex and preSMA reflected an integrative role that was sensitive to both inhibitory and attentional stimulus properties. At the level of neurofunctional networks, neural synchrony in the theta band (4–7 Hz) revealed interactions between principal cortical regions subserving attentional and inhibitory processes. Together, these results underscore the dynamic, integrative processing stages underlying inhibitory control.

The orienting reaction (OR) towards a new stimulus is subject to habituation, i.e., progressively attenuates with stimulus repetition. The skin conductance responses (SCRs) are known to represent a reliable measure of OR at the peripheral level. Yet, it is still a matter of debate which of the P3 subcomponents is the most likely to represent the central counterpart of the OR. The aim of the present work was to study habituation, recovery, and dishabituation phenomena intrinsic to a two-stimulus auditory oddball paradigm, one of the most-used paradigms both in research and clinic, by simultaneously recording SCRs and P3 in twenty healthy volunteers. Our findings show that the target stimulus was capable of triggering a more marked OR, as indexed by both SCRs and P3, compared to the standard stimulus, that could be due to its affective saliency and relevance for task completion; the application of temporal principal components analysis (PCA) to the P3 complex allowed us to identify several subcomponents including both early and late P3a (eP3a; lP3a), P3b, novelty P3 (nP3), and both a positive and a negative Slow Wave (+SW; −SW). Particularly, lP3a and P3b subcomponents showed a similar behavior to that observed for SCRs , suggesting them as central counterparts of OR. Finally, the P3 evoked by the first standard stimulus after the target showed a significant dishabituation phenomenon which could represent a sign of the local stimulus change. However, it did not reach a sufficient level to trigger an SCR/OR since it did not represent a salient event in the context of the task.

In a repetition-change paradigm it was explored whether the skin conductance response (SCR) and the heart rate (HR) response similarly reflect involuntary and voluntary orienting. Seven orienting stimuli, consisting of six contextually novel stimuli and one novel change, were presented to 144 participants. In order to evoke voluntary orienting, the signal value of the contextually novel stimuli was manipulated by task instruction. Results suggest that the SCR is a manifestation of the involuntary orienting response (iOR). The HR, however, showed a non-uniform pattern of response and turned out to be susceptible to voluntary orienting. While it responded to the last orienting stimulus, the novel change, with a clear-cut deceleration, the response to the first orienting stimulus had a polyphase structure and was sensitive to repetition and signal value. The HR response is, thus, of limited value as an indicator of the iOR because of its striking susceptibility to voluntary orienting.

This study aims to investigate how older adults react to a failed-inhibition error while performing a stop-signal task. That is, whether elderly people would exhibit enlarged post-error slowing and whether such slowing revealed an adaptive process, maladaptive process, or a mixture of maladaptive followed by adaptive processes. This study also addresses if the post-error process might further interact with a stimulus repetition effect based on the memory retrieval explanation. A group of 34 younger adults (age range 20–30 years) and a group of 34 older adults (age range 60–80 years) were included for the analyses. The results of the current study supported a mixture model by showing that older adults exhibited a larger post-error slowing than younger adults, and their post-error slowing was initially accompanied by deceased accuracy that then increased on the subsequent trial. Furthermore, such post-error slowing on older adults only occurred in the trial condition where the stimulus was repeated from the previous trial suggesting a memory-based process (a form of negative priming) involved in post-error processes. The implication of the current finding is that older adults might maintain the ability to detect and monitor the response error, yet their post-error adjustment might require a much longer time to start functioning well after the initial detrimental orienting response to the error and the entire process was memory-based.