Poster No:
2058
Submission Type:
Abstract Submission
Authors:
Monica Biggio1, Costanza Iester2, Ambra Bisio3, Sabrina Brigadoi4, Simone Cutini4, Laura Bonzano2, Marco Bove5
Institutions:
1Università degli studi di Genova, Genova, Italy, 2Department of Neuroscience, DINOGMI, University of Genoa, Genoa, Italy, Genova, Italy, 3DIMES, Section of Human Physiology, University of Genoa, Genova, Liguria, Italy, Genova, Italy, 4Department of Developmental Psychology, University of Padova, Padova, Italy, Padova, Italy, 5DIMES, University of Genoa, Genova, Italy
First Author:
Co-Author(s):
Costanza Iester
Department of Neuroscience, DINOGMI, University of Genoa, Genoa, Italy
Genova, Italy
Ambra Bisio
DIMES, Section of Human Physiology, University of Genoa, Genova, Liguria, Italy
Genova, Italy
Sabrina Brigadoi
Department of Developmental Psychology, University of Padova, Padova, Italy
Padova, Italy
Simone Cutini
Department of Developmental Psychology, University of Padova, Padova, Italy
Padova, Italy
Laura Bonzano
Department of Neuroscience, DINOGMI, University of Genoa, Genoa, Italy
Genova, Italy
Marco Bove
DIMES, University of Genoa
Genova, Italy
Introduction:
Hand Blink Reflex (HBR) is a subcortical defensive reflex evoked by the stimulation of the median nerve at the wrist1. Its intensity increases when the stimulated hand is placed near the face, inside the boundaries of the defensive peripersonal space of the face (DPPS). Therefore, along with the brainstem circuit mediating the blink reflex, a top-down modulation of HBR has been proposed, particularly in ventral intraparietal (VIP) and polysensory zone (PZ), areas related to DPPS representation. Here we aim to verify this hypothesis for the first time with the use of functional Near-Infrared Spectroscopy (fNIRS).
Methods:
Twenty-eight healthy participants (Age: 23 ± 0.57 years) were recruited for a session of non-invasive electromyography (EMG). HBR was evoked by administering transcutaneous electrical stimuli (ES) to the right median nerve of the wrist in two target positions with respect to the face: i.e., when the elbow angle was: 10◦ less than the maximal arm extension (FAR position) and 10◦ more than the maximal elbow flexion (NEAR position). Stimulus intensity was adjusted to elicit in each participant clear HBR responses (mean stimulus intensity: 7mA ± 0.52). Reflex responses were recorded bilaterally from orbicularis oculi muscles. Fifteen HBR responses were recorded from both positions for a total of thirty trials. Simultaneously, we performed an fNIRS acquisition to investigate the cortical activity immediately preceding the ES (PRE-STIMULUS_) and immediately after the ES, containing the HBR response (STIMULUS_) in the two positions. Optodes were arranged resulting in a total of 44 standard channels (3cm) and 8 short-separation channels. For each participant the fNIRS signal was pre-processed: channels with low signal–to–noise ratio were discarded; intensity data were converted to attenuation changes and motion artifacts were corrected by applying spline2 and wavelet3 motion correction techniques; a band-pass filter (0.01-3 Hz) was applied, and the mean hemodynamic response for each task block, participant and channel was recovered using a general linear model approach. This also led to removing physiological noise by regressing the most correlated short-separation channel from each standard channel. Then, we averaged channels belonging to the same Brodmann's area (BA) obtaining 11 regions of interest. The mean values of Oxy-hemoglobin (HbO) responses were computed for all BAs in an interval of 10 seconds before the stimulus onset in PRE-STIMULUS_ and after the stimulus onset in STIMULUS_ condition.
Results:
Participants showed a significantly increased HBR response when evoked in NEAR, with respect to FAR (Fig 1), as shown in previous literature1,4.
PRE-STIMULUS analysis showed a significant effect of POSITION, i.e. an overall lower cortical activity in PRE-STIMULUS_FAR with respect to PRE-STIMULUS_NEAR. Also, a significant POSITION * BA interaction indicated a greater activity in BA4 and 3 in PRE-STIMULUS_NEAR. In STIMULUS condition, significant effects of BA and HEMISPHERE were found, indicating greater activation of BA4 and 3, in particular in the left hemisphere, and a significant deactivation of BA44 in the NEAR with respect to the FAR condition (Fig 2).
Conclusions:
Stimulus preparation varies according to arm position, particularly in somatosensory and motor areas, predisposing the system to an increased response, or conversely deactivating the system when a response is not required, in a "energy saving" mechanism when the stimulus is implicitly perceived as not risky4. These areas remain active after stimulus reception, with no significant difference between positions. After the stimulus BA44, corresponding to the inferior frontal Gyrus, appears to be deactivated. BA44 has been associated with the judgement of the position of visual and somatosensory stimuli relative to their body midline5, and also with risk assessment and aversion6. At present it has not been possible to confirm the involvement of the VIP-PZ circuit in HBR modulation.
Motor Behavior:
Motor Behavior Other 1
Novel Imaging Acquisition Methods:
NIRS 2
Keywords:
Cortex
ELECTROPHYSIOLOGY
Near Infra-Red Spectroscopy (NIRS)
Nerves
Peripheral Nerve
1|2Indicates the priority used for review
Provide references using author date format
1. Sambo, C.F. (2012). 'Defensive peripersonal space: the blink reflex evoked by hand stimulation is increased when the hand is near the face.' Journal Neurophysiology. 107, 880–9.
2. Scholkmann, F. (2010). 'How to detect and reduce movement artifacts in near-infrared imaging using moving standard deviation and spline interpolation.' Physiological Measurement. 31, 649–662.
3. Molavi, B. (2012). 'Wavelet-based motion artifact removal for functional near-infrared spectroscopy.' Physiological Measurement. 33, 259–270.
4. Bisio, A. (2017). 'Dynamic Shaping of the Defensive Peripersonal Space through Predictive Motor Mechanisms: When the “Near” Becomes “Far.”' Journal Neuroscience. 37, 2415–2424.
5. Rizzolatti, G. (2002). 'Motor and cognitive functions of the ventral premotor cortex.' Current Opinion in Neurobiology. 12, 149–154.
6. Christopoulos, G.I. (2009). Neural correlates of value, risk, and risk aversion contributing to decision making under risk. Journal Neuroscience. 29, 12574–12583.