Cerebellar direct current stimulation modulates hand blink reflex: implications for defensive behavior in humans
The cerebellum is involved in a wide number of integrative functions. We evaluated the role of cerebellum in peripersonal defensive behavior, as assessed by the so‐called hand blink reflex (HBR), modulating cerebellar activity with transcranial direct current stimulation (tDCS). Healthy subjects und...
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Published in | Physiological reports Vol. 6; no. 10; pp. e13471 - n/a |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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John Wiley & Sons, Inc
01.05.2018
John Wiley and Sons Inc |
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Abstract | The cerebellum is involved in a wide number of integrative functions. We evaluated the role of cerebellum in peripersonal defensive behavior, as assessed by the so‐called hand blink reflex (HBR), modulating cerebellar activity with transcranial direct current stimulation (tDCS). Healthy subjects underwent cerebellar (sham, anodal, and cathodal tcDCS) and motor cortex tDCS (anodal or cathodal; 20′, 2 mA). For the recording of HBR, electrical stimuli were delivered using a surface bipolar electrode placed on the median nerve at the wrist and EMG activity recorded from the orbicularis oculi muscle bilaterally. Depending on the hand position respective to the face, HBR was assessed in four different conditions: “hand‐far,” “hand‐near” (eyes open), “side hand,” and “hand‐patched” (eyes closed). While sham and cathodal cerebellar stimulation had no significant effect, anodal tcDCS dramatically dampened the magnitude of the HBR, as measured by the area under the curve (AUC), in the “hand‐patched” and “side hand” conditions only, for ipsilateral (F(4,171) = 15.08, P < 0.0001; F(4,171) = 8.95, P < 0.0001) as well as contralateral recordings (F(4,171) = 17.96, P < 0.0001); F4,171) = 5.35, P = 0.0004). Cerebellar polarization did not modify AUC in the “hand‐far” and “hand‐near” sessions. tDCS applied over the motor area did not affect HBR. These results seem to support a role of the cerebellum in the defensive responses within the peripersonal space surrounding the face, thus suggesting a possible cerebellar involvement in visual‐independent defensive behavior.
We evaluated the role of cerebellum in peripersonal defensive behavior. Cerebellum modulates defensive behavior when the visual feedback is missing. Cerebellum may be involved in visual‐independent learning of defensive behavior. |
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AbstractList | The cerebellum is involved in a wide number of integrative functions. We evaluated the role of cerebellum in peripersonal defensive behavior, as assessed by the so-called hand blink reflex (HBR), modulating cerebellar activity with transcranial direct current stimulation (tDCS). Healthy subjects underwent cerebellar (sham, anodal, and cathodal tcDCS) and motor cortex tDCS (anodal or cathodal; 20', 2 mA). For the recording of HBR, electrical stimuli were delivered using a surface bipolar electrode placed on the median nerve at the wrist and EMG activity recorded from the orbicularis oculi muscle bilaterally. Depending on the hand position respective to the face, HBR was assessed in four different conditions: "hand-far," "hand-near" (eyes open), "side hand," and "hand-patched" (eyes closed). While sham and cathodal cerebellar stimulation had no significant effect, anodal tcDCS dramatically dampened the magnitude of the HBR, as measured by the area under the curve (AUC), in the "hand-patched" and "side hand" conditions only, for ipsilateral (F
= 15.08, P < 0.0001; F
= 8.95, P < 0.0001) as well as contralateral recordings (F
= 17.96, P < 0.0001); F
= 5.35, P = 0.0004). Cerebellar polarization did not modify AUC in the "hand-far" and "hand-near" sessions. tDCS applied over the motor area did not affect HBR. These results seem to support a role of the cerebellum in the defensive responses within the peripersonal space surrounding the face, thus suggesting a possible cerebellar involvement in visual-independent defensive behavior. The cerebellum is involved in a wide number of integrative functions. We evaluated the role of cerebellum in peripersonal defensive behavior, as assessed by the so‐called hand blink reflex (HBR), modulating cerebellar activity with transcranial direct current stimulation (tDCS). Healthy subjects underwent cerebellar (sham, anodal, and cathodal tcDCS) and motor cortex tDCS (anodal or cathodal; 20′, 2 mA). For the recording of HBR, electrical stimuli were delivered using a surface bipolar electrode placed on the median nerve at the wrist and EMG activity recorded from the orbicularis oculi muscle bilaterally. Depending on the hand position respective to the face, HBR was assessed in four different conditions: “hand‐far,” “hand‐near” (eyes open), “side hand,” and “hand‐patched” (eyes closed). While sham and cathodal cerebellar stimulation had no significant effect, anodal tcDCS dramatically dampened the magnitude of the HBR, as measured by the area under the curve (AUC), in the “hand‐patched” and “side hand” conditions only, for ipsilateral (F(4,171) = 15.08, P < 0.0001; F(4,171) = 8.95, P < 0.0001) as well as contralateral recordings (F(4,171) = 17.96, P < 0.0001); F4,171) = 5.35, P = 0.0004). Cerebellar polarization did not modify AUC in the “hand‐far” and “hand‐near” sessions. tDCS applied over the motor area did not affect HBR. These results seem to support a role of the cerebellum in the defensive responses within the peripersonal space surrounding the face, thus suggesting a possible cerebellar involvement in visual‐independent defensive behavior. The cerebellum is involved in a wide number of integrative functions. We evaluated the role of cerebellum in peripersonal defensive behavior, as assessed by the so-called hand blink reflex (HBR), modulating cerebellar activity with transcranial direct current stimulation (tDCS). Healthy subjects underwent cerebellar (sham, anodal, and cathodal tcDCS) and motor cortex tDCS (anodal or cathodal; 20', 2 mA). For the recording of HBR, electrical stimuli were delivered using a surface bipolar electrode placed on the median nerve at the wrist and EMG activity recorded from the orbicularis oculi muscle bilaterally. Depending on the hand position respective to the face, HBR was assessed in four different conditions: "hand-far," "hand-near" (eyes open), "side hand," and "hand-patched" (eyes closed). While sham and cathodal cerebellar stimulation had no significant effect, anodal tcDCS dramatically dampened the magnitude of the HBR, as measured by the area under the curve (AUC), in the "hand-patched" and "side hand" conditions only, for ipsilateral (F(4,171) = 15.08, P < 0.0001; F(4,171) = 8.95, P < 0.0001) as well as contralateral recordings (F(4,171) = 17.96, P < 0.0001); F4,171) = 5.35, P = 0.0004). Cerebellar polarization did not modify AUC in the "hand-far" and "hand-near" sessions. tDCS applied over the motor area did not affect HBR. These results seem to support a role of the cerebellum in the defensive responses within the peripersonal space surrounding the face, thus suggesting a possible cerebellar involvement in visual-independent defensive behavior.The cerebellum is involved in a wide number of integrative functions. We evaluated the role of cerebellum in peripersonal defensive behavior, as assessed by the so-called hand blink reflex (HBR), modulating cerebellar activity with transcranial direct current stimulation (tDCS). Healthy subjects underwent cerebellar (sham, anodal, and cathodal tcDCS) and motor cortex tDCS (anodal or cathodal; 20', 2 mA). For the recording of HBR, electrical stimuli were delivered using a surface bipolar electrode placed on the median nerve at the wrist and EMG activity recorded from the orbicularis oculi muscle bilaterally. Depending on the hand position respective to the face, HBR was assessed in four different conditions: "hand-far," "hand-near" (eyes open), "side hand," and "hand-patched" (eyes closed). While sham and cathodal cerebellar stimulation had no significant effect, anodal tcDCS dramatically dampened the magnitude of the HBR, as measured by the area under the curve (AUC), in the "hand-patched" and "side hand" conditions only, for ipsilateral (F(4,171) = 15.08, P < 0.0001; F(4,171) = 8.95, P < 0.0001) as well as contralateral recordings (F(4,171) = 17.96, P < 0.0001); F4,171) = 5.35, P = 0.0004). Cerebellar polarization did not modify AUC in the "hand-far" and "hand-near" sessions. tDCS applied over the motor area did not affect HBR. These results seem to support a role of the cerebellum in the defensive responses within the peripersonal space surrounding the face, thus suggesting a possible cerebellar involvement in visual-independent defensive behavior. The cerebellum is involved in a wide number of integrative functions. We evaluated the role of cerebellum in peripersonal defensive behavior, as assessed by the so‐called hand blink reflex (HBR), modulating cerebellar activity with transcranial direct current stimulation (tDCS). Healthy subjects underwent cerebellar (sham, anodal, and cathodal tcDCS) and motor cortex tDCS (anodal or cathodal; 20′, 2 mA). For the recording of HBR, electrical stimuli were delivered using a surface bipolar electrode placed on the median nerve at the wrist and EMG activity recorded from the orbicularis oculi muscle bilaterally. Depending on the hand position respective to the face, HBR was assessed in four different conditions: “hand‐far,” “hand‐near” (eyes open), “side hand,” and “hand‐patched” (eyes closed). While sham and cathodal cerebellar stimulation had no significant effect, anodal tcDCS dramatically dampened the magnitude of the HBR, as measured by the area under the curve (AUC), in the “hand‐patched” and “side hand” conditions only, for ipsilateral (F(4,171) = 15.08, P < 0.0001; F(4,171) = 8.95, P < 0.0001) as well as contralateral recordings (F(4,171) = 17.96, P < 0.0001); F4,171) = 5.35, P = 0.0004). Cerebellar polarization did not modify AUC in the “hand‐far” and “hand‐near” sessions. tDCS applied over the motor area did not affect HBR. These results seem to support a role of the cerebellum in the defensive responses within the peripersonal space surrounding the face, thus suggesting a possible cerebellar involvement in visual‐independent defensive behavior. We evaluated the role of cerebellum in peripersonal defensive behavior. Cerebellum modulates defensive behavior when the visual feedback is missing. Cerebellum may be involved in visual‐independent learning of defensive behavior. The cerebellum is involved in a wide number of integrative functions. We evaluated the role of cerebellum in peripersonal defensive behavior, as assessed by the so‐called hand blink reflex ( HBR ), modulating cerebellar activity with transcranial direct current stimulation ( tDCS ). Healthy subjects underwent cerebellar (sham, anodal, and cathodal tc DCS ) and motor cortex tDCS (anodal or cathodal; 20′, 2 mA). For the recording of HBR , electrical stimuli were delivered using a surface bipolar electrode placed on the median nerve at the wrist and EMG activity recorded from the orbicularis oculi muscle bilaterally. Depending on the hand position respective to the face, HBR was assessed in four different conditions: “hand‐far,” “hand‐near” (eyes open), “side hand,” and “hand‐patched” (eyes closed). While sham and cathodal cerebellar stimulation had no significant effect, anodal tc DCS dramatically dampened the magnitude of the HBR , as measured by the area under the curve ( AUC ), in the “hand‐patched” and “side hand” conditions only, for ipsilateral ( F (4,171) = 15.08, P < 0.0001; F (4,171) = 8.95, P < 0.0001) as well as contralateral recordings ( F (4,171) = 17.96, P < 0.0001); F 4,171) = 5.35, P = 0.0004). Cerebellar polarization did not modify AUC in the “hand‐far” and “hand‐near” sessions. tDCS applied over the motor area did not affect HBR . These results seem to support a role of the cerebellum in the defensive responses within the peripersonal space surrounding the face, thus suggesting a possible cerebellar involvement in visual‐independent defensive behavior. |
Author | Bocci, Tommaso Barloscio, Davide Priori, Alberto Sartucci, Ferdinando Ferrucci, Roberta Parenti, Laura Cortese, Francesca |
AuthorAffiliation | 6 Neuroscience Institute National Research Council Pisa Italy 4 Department of Neurological Sciences University of Milan Fondazione IRCCS Ospedale Maggiore Policlinico Milan Italy 1 Department of Clinical and Experimental Medicine Cisanello Neurology Unit Pisa University Medical School Pisa Italy 5 Department of Medical‐Surgical Sciences and Biotechonologies Sapienza University of Rome Rome Italy 2 Department of Medical‐Surgical Pathophysiology and Transplants University of Milan Milan Italy 3 Clinical Center for Neurotechnology Neurostimulation and Movement Disorders Fondazione IRCCS “Ca' Granda” Ospedale Maggiore di Milano Milan Italy |
AuthorAffiliation_xml | – name: 1 Department of Clinical and Experimental Medicine Cisanello Neurology Unit Pisa University Medical School Pisa Italy – name: 5 Department of Medical‐Surgical Sciences and Biotechonologies Sapienza University of Rome Rome Italy – name: 2 Department of Medical‐Surgical Pathophysiology and Transplants University of Milan Milan Italy – name: 3 Clinical Center for Neurotechnology Neurostimulation and Movement Disorders Fondazione IRCCS “Ca' Granda” Ospedale Maggiore di Milano Milan Italy – name: 6 Neuroscience Institute National Research Council Pisa Italy – name: 4 Department of Neurological Sciences University of Milan Fondazione IRCCS Ospedale Maggiore Policlinico Milan Italy |
Author_xml | – sequence: 1 givenname: Tommaso surname: Bocci fullname: Bocci, Tommaso organization: Fondazione IRCCS “Ca' Granda” Ospedale Maggiore di Milano – sequence: 2 givenname: Roberta surname: Ferrucci fullname: Ferrucci, Roberta organization: Fondazione IRCCS Ospedale Maggiore Policlinico – sequence: 3 givenname: Davide surname: Barloscio fullname: Barloscio, Davide organization: Pisa University Medical School – sequence: 4 givenname: Laura surname: Parenti fullname: Parenti, Laura organization: Pisa University Medical School – sequence: 5 givenname: Francesca surname: Cortese fullname: Cortese, Francesca organization: Sapienza University of Rome – sequence: 6 givenname: Alberto surname: Priori fullname: Priori, Alberto organization: Fondazione IRCCS Ospedale Maggiore Policlinico – sequence: 7 givenname: Ferdinando surname: Sartucci fullname: Sartucci, Ferdinando email: ferdinando.sartucci@med.unipi.it organization: National Research Council |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29845771$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s12311_019_01013_9 crossref_primary_10_1007_s12311_019_01020_w crossref_primary_10_1186_s12984_019_0581_1 crossref_primary_10_1038_s41598_021_84241_6 crossref_primary_10_4103_1673_5374_308083 crossref_primary_10_31083_j_jin2310195 crossref_primary_10_3389_fnins_2019_00412 |
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Keywords | peripersonal space defensive behavior hand blink reflex Cerebellar direct current stimulation tDCS cerebellum |
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Snippet | The cerebellum is involved in a wide number of integrative functions. We evaluated the role of cerebellum in peripersonal defensive behavior, as assessed by... |
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SubjectTerms | Adult Behavior Blink reflex Blinking Central Nervous System Cerebellar direct current stimulation Cerebellum Cerebellum - physiology Cognitive and Behavioural Neuroscience Consciousness Cortex (motor) Defensive behavior Electric Stimulation Electrical stimulation of the brain Electrical stimuli Electrodes Electromyography ESB Female Hand Hand - physiology hand blink reflex Humans Hypotheses Male Median nerve Median Nerve - physiology Motor Control Motor Cortex - physiology Original Research peripersonal space Personal Space Physiology tDCS Transcranial Direct Current Stimulation Visual cortex Wrist Young Adult |
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Title | Cerebellar direct current stimulation modulates hand blink reflex: implications for defensive behavior in humans |
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