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1.
Rhinology ; 2024 Jul 01.
Article in English | MEDLINE | ID: mdl-38950382

ABSTRACT

BACKGROUND: Persistent olfactory dysfunction (OD) is a common symptom following SARS-CoV-2 infection that can greatly impact quality of life (QoL). Because coping strategies have been shown to moderate the effect of disease symptoms on functional and affective outcomes, this study aims to determine whether specific coping strategies are associated with and moderate QoL outcomes. METHODOLOGY: Participants with prior SARS-CoV-2 infection underwent psychophysical olfactory testing with Sniffin' Sticks and completed questionnaires to elicit subjective olfactory function, coping strategies, olfactory-specific QoL, general QoL, and mental health. RESULTS: There were 93 participants included in the study. Olfactory specific QoL scores were significantly worse among individuals with subjective and psychophysically measured OD compared to those with subjective and psychophysically confirmed normosmia. Olfactory-specific QoL, general QoL, and anxiety symptom scores were positively correlated with avoidant and disengagement coping among individuals with subjective and psychophysically measured OD. Depression symptom scores were positively correlated with avoidant and disengagement coping and negatively correlated with approach and engagement coping. There were no significant moderating effects on the association between olfactory performance and QoL or mental health screening assessment. CONCLUSIONS: Approach and engagement coping mechanisms are associated with improved depression, whereas avoidant and disengagement coping tracks with worse QoL and mental health screening assessment, offering an opportunity to counsel patients accordingly.

2.
Philos Trans R Soc Lond B Biol Sci ; 377(1863): 20210180, 2022 11 07.
Article in English | MEDLINE | ID: mdl-36126672

ABSTRACT

According to an evolutionist approach, laughter is a multifaceted behaviour affecting social, emotional, motor and speech functions. Albeit previous studies have suggested that high-frequency electrical stimulation (HF-ES) of the pregenual anterior cingulate cortex (pACC) may induce bursts of laughter-suggesting a crucial contribution of this region to the cortical control of this behaviour-the complex nature of laughter implies that outward connections from the pACC may reach and affect a complex network of frontal and limbic regions. Here, we studied the effective connectivity of the pACC by analysing the cortico-cortical evoked potentials elicited by single-pulse electrical stimulation of pACC sites whose HF-ES elicited laughter in 12 patients. Once these regions were identified, we studied their clinical response to HF-ES, to reveal the specific functional target of pACC representation of laughter. Results reveal that the neural representation of laughter in the pACC interacts with several frontal and limbic regions, including cingulate, orbitofrontal, medial prefrontal and anterior insular regions-involved in interoception, emotion, social reward and motor behaviour. These results offer neuroscientific support to the evolutionist approach to laughter, providing a possible mechanistic explanation of the interplay between this behaviour and emotion regulation, speech production and social interactions. This article is part of the theme issue 'Cracking the laugh code: laughter through the lens of biology, psychology and neuroscience'.


Subject(s)
Gyrus Cinguli , Laughter , Electric Stimulation/methods , Emotions/physiology , Evoked Potentials , Gyrus Cinguli/physiology , Humans , Laughter/physiology , Laughter/psychology
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
5.
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
6.
Cereb Cortex ; 27(8): 4229-4243, 2017 08 01.
Article in English | MEDLINE | ID: mdl-28525604

ABSTRACT

A description of the spatiotemporal dynamics of human cortical activity during cognitive tasks is a fundamental goal of neuroscience. In the present study, we employed stereo-EEG in order to assess the neural activity during tool-action observation. We recorded from 49 epileptic patients (5502 leads) implanted with intracerebral electrodes, while they observed tool and hand actions. We deconstructed actions into 3 events-video onset, action onset, and tool-object contact-and assessed how different brain regions respond to these events. Video onset, with actions not yet visible, recruited only visual areas. Aligning the responses at action onset, yielded activity in the parietal-frontal manipulation circuit and, selectively for tool actions, in the left anterior supramarginal gyrus (aSMG). Finally, by aligning to the tool-object contact that signals the achievement of the main goal of the observed action, activations were found in SII and dorsal premotor cortex. In conclusion, our data show that during tool-action observation, in addition to the general action observation network there is a selective activation of aSMG, which exhibits internally different patterns of responsiveness. In addition, neural responses selective for the contact between the tool and the object were also observed.


Subject(s)
Cerebral Cortex/physiology , Motion Perception/physiology , Motor Skills , Adult , Cerebral Cortex/physiopathology , Drug Resistant Epilepsy/physiopathology , Drug Resistant Epilepsy/surgery , Electrocorticography , Epilepsies, Partial/physiopathology , Epilepsies, Partial/surgery , Female , Gamma Rhythm , Hand , Humans , Male , Neuropsychological Tests , Photic Stimulation
7.
Neuropsychologia ; 89: 364-370, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27401930

ABSTRACT

Laughter and smile are typical expressions of mirth and fundamental means of social communication. Despite their general interest, the current knowledge about the brain regions involved in the production of these expressions is still very limited, and the principal insights come from electrical stimulation (ES) studies in patients, in which, nevertheless, laughter or smile have been elicited very rarely. Previous studies showed that laughter is evoked by the stimulation of nodes of an emotional network encompassing the anterior cingulate, the superior frontal and basal temporal cortex. A common feature of these stimulation studies is that the facial expression was always accompanied by motor awareness and often by mirth, in line with the affective functions attributed to these regions. Little is known, in contrast, on the neural basis of the voluntary motor control of this expression. The objective of this study was to investigate the effect of ES of the frontal operculum (FO), which is considered a crucial node for the linkage of the voluntary motor system for emotional expression and limbic emotional network. We report the case of ES applied to the frontal operculum (FO) in four patients with drug-resistant focal epilepsy undergoing stereo-electroencephalographic (SEEG) implantation of intracerebral electrodes. In all patients, ES applied to the FO produced laughter or smile. Interestingly, in one patient, the production of a smiling expression was also clearly accompanied by the lack of motor awareness. Since the lack of motor awareness has been previously observed only after the stimulation of the voluntary motor network, we speculate that FO is involved in the voluntary control of facial expressions, and is placed at the interface with the emotional network, gating limbic information to the motor system.


Subject(s)
Communication Disorders/therapy , Electric Stimulation/methods , Evoked Potentials/physiology , Frontal Lobe/physiology , Laughter , Smiling , Adult , Brain Mapping , Child, Preschool , Communication Disorders/diagnostic imaging , Communication Disorders/physiopathology , Electroencephalography , Female , Frontal Lobe/diagnostic imaging , Functional Laterality , Humans , Male , Tomography Scanners, X-Ray Computed , Young Adult
8.
Proc Natl Acad Sci U S A ; 105(6): 2209-13, 2008 Feb 12.
Article in English | MEDLINE | ID: mdl-18238904

ABSTRACT

The capacity to use tools is a fundamental evolutionary achievement. Its essence stands in the capacity to transfer a proximal goal (grasp a tool) to a distal goal (e.g., grasp food). Where and how does this goal transfer occur? Here, we show that, in monkeys trained to use tools, cortical motor neurons, active during hand grasping, also become active during grasping with pliers, as if the pliers were now the hand fingers. This motor embodiment occurs both for normal pliers and for "reverse pliers," an implement that requires finger opening, instead of their closing, to grasp an object. We conclude that the capacity to use tools is based on an inherently goal-centered functional organization of primate cortical motor areas.


Subject(s)
Motor Cortex/physiology , Neurons/physiology , Animals , Electromyography , Female , Macaca nemestrina , Male , Motor Cortex/cytology
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