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1.
Proc Natl Acad Sci U S A ; 118(44)2021 11 02.
Article in English | MEDLINE | ID: mdl-34716272

ABSTRACT

Actions with identical goals can be executed in different ways (gentle, rude, vigorous, etc.), which D. N. Stern called vitality forms [D. N. Stern, Forms of Vitality Exploring Dynamic Experience in Psychology, Arts, Psychotherapy, and Development (2010)]. Vitality forms express the agent's attitudes toward others. In a series of fMRI studies, we found that the dorso-central insula (DCI) is the region that is selectively active during both vitality form observation and execution. In one previous experiment, however, the middle cingulate gyrus also exhibited activation. In the present study, in order to assess the role of the cingulate cortex in vitality form processing, we adopted a classical vitality form paradigm, but making the control condition devoid of vitality forms using jerky movements. Participants performed two different tasks: Observation of actions performed gently or rudely and execution of the same actions. The results showed that in addition to the insula, the middle cingulate cortex (MCC) was strongly activated during both action observation and execution. Using a voxel-based analysis, voxels showing a similar trend of the blood-oxygen-level-dependent (BOLD) signal in both action observation and execution were found in the DCI and in the MCC. Finally, using a multifiber tractography analysis, we showed that the active sites in MCC and DCI are reciprocally connected.


Subject(s)
Behavior/physiology , Gyrus Cinguli/physiology , Insular Cortex/physiology , Adult , Attitude , Brain/physiology , Brain Mapping/methods , Cerebral Cortex/physiology , Female , Humans , Magnetic Resonance Imaging/methods , Male
2.
J Neural Eng ; 18(2)2021 02 26.
Article in English | MEDLINE | ID: mdl-33461177

ABSTRACT

Objective.Previous studies demonstrated the possibility to fabricate stereo-electroencephalography probes with high channel count and great design freedom, which incorporate macro-electrodes as well as micro-electrodes offering potential benefits for the pre-surgical evaluation of drug resistant epileptic patients. These new polyimide probes allowed to record local field potentials, multi- and single-unit activity (SUA) in the macaque monkey as early as 1 h after implantation, and yielded stable SUA for up to 26 d after implantation. The findings opened new perspectives for investigating mechanisms underlying focal epilepsy and its treatment, but before moving to possible human application, safety data are needed. In the present study we evaluate the tissue response of this new neural interface by assessing post-mortem the reaction of brain tissue along and around the probe implantation site.Approach.Three probes were implanted, independently, in the brain of one monkey (Macaca mulatta) at different times. We used specific immunostaining methods for visualizing neuronal cells and astrocytes, for measuring the extent of damage caused by the probe and for relating it with the implantation time.Main results.The size of the region where neurons cannot be detected did not exceed the size of the probe, indicating that a complete loss of neuronal cells is only present where the probe was physically positioned in the brain. Furthermore, around the probe shank, we observed a slightly reduced number of neurons within a radius of 50µm and a modest increase in the number of astrocytes within 100µm.Significance.In the light of previous electrophysiological findings, the present data suggest the potential usefulness and safety of this probe for human applications.


Subject(s)
Electroencephalography , Polymers , Animals , Electrodes, Implanted/adverse effects , Electroencephalography/methods , Macaca mulatta , Neurons/physiology
3.
Cereb Cortex ; 31(2): 899-916, 2021 01 05.
Article in English | MEDLINE | ID: mdl-32969467

ABSTRACT

Laughter is a complex motor behavior occurring in both emotional and nonemotional contexts. Here, we investigated whether the different functions of laughter are mediated by distinct networks and, if this is the case, which are the white matter tracts sustaining them. We performed a multifiber tractography investigation placing seeds in regions involved in laughter production, as identified by previous intracerebral electrical stimulation studies in humans: the pregenual anterior cingulate (pACC), ventral temporal pole (TPv), frontal operculum (FO), presupplementary motor cortex, and ventral striatum/nucleus accumbens (VS/NAcc). The primary motor cortex (M1) and two subcortical territories were also studied to trace the descending projections. Results provided evidence for the existence of two relatively distinct networks. A first network, including pACC, TPv, and VS/NAcc, is interconnected through the anterior cingulate bundle, the accumbofrontal tract, and the uncinate fasciculus, reaching the brainstem throughout the mamillo-tegmental tract. This network is likely involved in the production of emotional laughter. A second network, anchored to FO and M1, projects to the brainstem motor nuclei through the internal capsule. It is most likely the neural basis of nonemotional and conversational laughter. The two networks interact throughout the pre-SMA that is connected to both pACC and FO.


Subject(s)
Diffusion Tensor Imaging/methods , Laughter/physiology , Laughter/psychology , Nerve Net/diagnostic imaging , Nerve Net/physiology , Adult , Brain Mapping , Brain Stem/physiology , Cerebral Cortex/diagnostic imaging , Cerebral Cortex/physiology , Electric Stimulation , Emotions/physiology , Female , Gyrus Cinguli/diagnostic imaging , Gyrus Cinguli/physiology , Humans , Male , Nucleus Accumbens/diagnostic imaging , Nucleus Accumbens/physiology , Ventral Striatum/diagnostic imaging , Ventral Striatum/physiology , White Matter/diagnostic imaging , Young Adult
4.
Cereb Cortex ; 29(5): 2140-2147, 2019 05 01.
Article in English | MEDLINE | ID: mdl-29741595

ABSTRACT

It has been recently found that the human dorso-central insular cortex contributes to the execution and recognition of the affective component of hand actions, most likely through modulation of the activity of the parieto-frontal circuits. While the anatomical connections between the hand representation of the insula and, the parietal and frontal regions controlling reaching/grasping actions is well assessed in the monkey, it is unknown the existence of a homolog circuit in humans. In the present study, we performed a multifiber tractography investigation to trace the tracts possibly connecting the insula to the parieto-frontal circuits by locating seeds in the parietal, premotor, and prefrontal nodes of the reaching/grasping network, in both humans and monkeys. Results showed that, in both species, the insula is connected with the cortical action execution/recognition circuit by similar white matter tracts, running in parallel to the third branch of the superior longitudinal fasciculus and the anterior segment of the arcuate fasciculus.


Subject(s)
Arm/physiology , Cerebral Cortex/anatomy & histology , Frontal Lobe/anatomy & histology , Motor Activity , Parietal Lobe/anatomy & histology , Animals , Cerebral Cortex/physiology , Diffusion Magnetic Resonance Imaging , Female , Frontal Lobe/physiology , Humans , Macaca mulatta , Male , Neural Pathways/anatomy & histology , Neural Pathways/physiology , Parietal Lobe/physiology , Species Specificity , White Matter/anatomy & histology , White Matter/physiology
5.
Sci Rep ; 7(1): 8571, 2017 08 17.
Article in English | MEDLINE | ID: mdl-28819117

ABSTRACT

Following gaze is a crucial skill, in primates, for understanding where and at what others are looking, and often requires head rotation. The neural basis underlying head rotation are deemed to overlap with the parieto-frontal attention/gaze-shift network. Here, we show that a set of neurons in monkey's Brodmann area 9/46dr (BA 9/46dr), which is involved in orienting processes and joint attention, becomes active during self head rotation and that the activity of these neurons cannot be accounted for by saccade-related activity (head-rotation neurons). Another set of BA 9/46dr neurons encodes head rotation performed by an observed agent facing the monkey (visually triggered neurons). Among these latter neurons, almost half exhibit the intriguing property of encoding both execution and observation of head rotation (mirror-like neurons). Finally, by means of neuronal tracing techniques, we showed that BA 9/46dr takes part into two distinct networks: a dorso/mesial network, playing a role in spatial head/gaze orientation, and a ventrolateral network, likely involved in processing social stimuli and mirroring others' head. The overall results of this study provide a new, comprehensive picture of the role of BA 9/46dr in encoding self and others' head rotation, likely playing a role in head-following behaviors.


Subject(s)
Head Movements/physiology , Macaca fascicularis/physiology , Macaca mulatta/physiology , Neurons/physiology , Prefrontal Cortex/physiology , Action Potentials/physiology , Animals , Attention/physiology , Female , Fixation, Ocular/physiology , Neurons/cytology , Orientation, Spatial/physiology , Prefrontal Cortex/cytology , Psychomotor Performance/physiology , Rotation , Saccades/physiology , Visual Perception/physiology
6.
Neuroscience ; 358: 300-315, 2017 09 01.
Article in English | MEDLINE | ID: mdl-28687313

ABSTRACT

The vast majority of functional studies investigating mirror neurons (MNs) explored their properties in relation to hand actions, and very few investigated how MNs respond to mouth actions or communicative gestures. Since hand and mouth MNs were recorded in two partially overlapping sectors of the ventral precentral cortex of the macaque monkey, there is a general assumption that they share a same neuroanatomical network, with the parietal cortex as a main source of visual information. In the current review, we challenge this perspective and describe the connectivity pattern of mouth MN sector. The mouth MNs F5/opercular region is connected with premotor, parietal areas mostly related to the somatosensory and motor representation of the face/mouth, and with area PrCO, involved in processing gustatory and somatosensory intraoral input. Unlike hand MNs, mouth MNs do not receive their visual input from parietal regions. Such information related to face/communicative behaviors could come from the ventrolateral prefrontal cortex. Further strong connections derive from limbic structures involved in encoding emotional facial expressions and motivational/reward processing. These brain structures include the anterior cingulate cortex, the anterior and mid-dorsal insula, orbitofrontal cortex and the basolateral amygdala. The mirror mechanism is therefore composed and supported by at least two different anatomical pathways: one is concerned with sensorimotor transformation in relation to reaching and hand grasping within the traditional parietal-premotor circuits; the second one is linked to the mouth/face motor control and is connected with limbic structures, involved in communication/emotions and reward processing.


Subject(s)
Face/innervation , Hand/innervation , Limbic System/cytology , Mirror Neurons/physiology , Neural Pathways/physiology , Sensorimotor Cortex/cytology , Animals , Humans , Limbic System/physiology , Sensorimotor Cortex/physiology
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