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auditory steady state responses (assrs)  (Wolters Kluwer Health)

 
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    Wolters Kluwer Health auditory steady state responses (assrs)
    Auditory Steady State Responses (Assrs), supplied by Wolters Kluwer Health, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Article Title: Stability of Auditory Steady State Responses Over Time
    Article Snippet: 0196/0202/16/XXXX-00/0 • Ear & Hearing • Copyright © 2017 Wolters Kluwer Health, Inc. All rights reserved • Printed in the U.S.A. 1 Objectives: Auditory steady state responses (ASSRs) are used in clinical practice for objective hearing assessments.

    Article Title: Binaural Interaction Effects of 30–50 Hz Auditory Steady State Responses
    Article Snippet: e305 Objectives: Auditory stimuli modulated by modulation frequencies within the 30 to 50 Hz region evoke auditory steady state responses (ASSRs) with high signal to noise ratios in adults, and can be used to determine the frequency-specific hearing thresholds of adults who are unable to give behavioral feedback reliably.. To measure ASSRs as efficiently as possible a multiple stimulus paradigm can be used, stimulating both ears simultaneously.. The response strength of 30 to 50Hz ASSRs is, however, affected when both ears are stimulated simultaneously.



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    (A) Scheme showing the treatment regime used to study the effect of subchronic PCP on cognition using the T-Maze alternation task; on <t>ASSR</t> using electroencephalography (EEG); on local mPFC network using ex vivo electrophysiology (EPhys) and immunohistochemistry (IHC) of PV; on the long-range inputs from vHPC to mPFC using optogenetics; and on brain networks using functional ultrasound imaging (fUS). Different cohorts of mice were used for each experiment. (B) Percent of spontaneous alternation of vehicle- and PCP treated mice in the T-Maze task at day 21 (for Vh, mean spontaneous alternation: 70.3 ± 3.2 %, n= 9 mice; for PCP: 60.4 ± 8.9%, n= 15 mice; Mann-Whitney U test: U = 31.5, p = 0.03). (C) Heatmaps of phase-lock ratio (left) in 40 Hz ASSR from the mPFC of vehicle- and PCP treated animals and quantifications at day 24 (for Vh, mean ratio: 0.33 ± 0.046, n= 5 mice; for PCP: 0.462 ± 0.029, n= 9 mice; Mann-Whitney U test: U = 8, p = 0.0599) day 31 (for Vh, mean ratio: 0.27 ± 0.065, n= 6 mice; for PCP: 0.423 ± 0.035, n= 8 mice; Mann-Whitney U test: U = 7, p = 0.293); day 34 (for Vh, mean ratio: 0.32 ± 0.0627, n= 4 mice; for PCP: 0.3625 ± 0.030, n= 9 mice; Mann-Whitney U test: U = 12, p = 0.207) and day 40 (for Vh, mean ratio: 0.318 ± 0.071, n= 6 mice; for PCP: 0.318 ± 0.034, n= 9 mice; Mann-Whitney U test: U = 26, p = 0.964). Each dot is the quantification of a single animal.
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    (A) Scheme showing the treatment regime used to study the effect of subchronic PCP on cognition using the T-Maze alternation task; on <t>ASSR</t> using electroencephalography (EEG); on local mPFC network using ex vivo electrophysiology (EPhys) and immunohistochemistry (IHC) of PV; on the long-range inputs from vHPC to mPFC using optogenetics; and on brain networks using functional ultrasound imaging (fUS). Different cohorts of mice were used for each experiment. (B) Percent of spontaneous alternation of vehicle- and PCP treated mice in the T-Maze task at day 21 (for Vh, mean spontaneous alternation: 70.3 ± 3.2 %, n= 9 mice; for PCP: 60.4 ± 8.9%, n= 15 mice; Mann-Whitney U test: U = 31.5, p = 0.03). (C) Heatmaps of phase-lock ratio (left) in 40 Hz ASSR from the mPFC of vehicle- and PCP treated animals and quantifications at day 24 (for Vh, mean ratio: 0.33 ± 0.046, n= 5 mice; for PCP: 0.462 ± 0.029, n= 9 mice; Mann-Whitney U test: U = 8, p = 0.0599) day 31 (for Vh, mean ratio: 0.27 ± 0.065, n= 6 mice; for PCP: 0.423 ± 0.035, n= 8 mice; Mann-Whitney U test: U = 7, p = 0.293); day 34 (for Vh, mean ratio: 0.32 ± 0.0627, n= 4 mice; for PCP: 0.3625 ± 0.030, n= 9 mice; Mann-Whitney U test: U = 12, p = 0.207) and day 40 (for Vh, mean ratio: 0.318 ± 0.071, n= 6 mice; for PCP: 0.318 ± 0.034, n= 9 mice; Mann-Whitney U test: U = 26, p = 0.964). Each dot is the quantification of a single animal.
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    (A) Scheme showing the treatment regime used to study the effect of subchronic PCP on cognition using the T-Maze alternation task; on <t>ASSR</t> using electroencephalography (EEG); on local mPFC network using ex vivo electrophysiology (EPhys) and immunohistochemistry (IHC) of PV; on the long-range inputs from vHPC to mPFC using optogenetics; and on brain networks using functional ultrasound imaging (fUS). Different cohorts of mice were used for each experiment. (B) Percent of spontaneous alternation of vehicle- and PCP treated mice in the T-Maze task at day 21 (for Vh, mean spontaneous alternation: 70.3 ± 3.2 %, n= 9 mice; for PCP: 60.4 ± 8.9%, n= 15 mice; Mann-Whitney U test: U = 31.5, p = 0.03). (C) Heatmaps of phase-lock ratio (left) in 40 Hz ASSR from the mPFC of vehicle- and PCP treated animals and quantifications at day 24 (for Vh, mean ratio: 0.33 ± 0.046, n= 5 mice; for PCP: 0.462 ± 0.029, n= 9 mice; Mann-Whitney U test: U = 8, p = 0.0599) day 31 (for Vh, mean ratio: 0.27 ± 0.065, n= 6 mice; for PCP: 0.423 ± 0.035, n= 8 mice; Mann-Whitney U test: U = 7, p = 0.293); day 34 (for Vh, mean ratio: 0.32 ± 0.0627, n= 4 mice; for PCP: 0.3625 ± 0.030, n= 9 mice; Mann-Whitney U test: U = 12, p = 0.207) and day 40 (for Vh, mean ratio: 0.318 ± 0.071, n= 6 mice; for PCP: 0.318 ± 0.034, n= 9 mice; Mann-Whitney U test: U = 26, p = 0.964). Each dot is the quantification of a single animal.
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    (A) Scheme showing the treatment regime used to study the effect of subchronic PCP on cognition using the T-Maze alternation task; on <t>ASSR</t> using electroencephalography (EEG); on local mPFC network using ex vivo electrophysiology (EPhys) and immunohistochemistry (IHC) of PV; on the long-range inputs from vHPC to mPFC using optogenetics; and on brain networks using functional ultrasound imaging (fUS). Different cohorts of mice were used for each experiment. (B) Percent of spontaneous alternation of vehicle- and PCP treated mice in the T-Maze task at day 21 (for Vh, mean spontaneous alternation: 70.3 ± 3.2 %, n= 9 mice; for PCP: 60.4 ± 8.9%, n= 15 mice; Mann-Whitney U test: U = 31.5, p = 0.03). (C) Heatmaps of phase-lock ratio (left) in 40 Hz ASSR from the mPFC of vehicle- and PCP treated animals and quantifications at day 24 (for Vh, mean ratio: 0.33 ± 0.046, n= 5 mice; for PCP: 0.462 ± 0.029, n= 9 mice; Mann-Whitney U test: U = 8, p = 0.0599) day 31 (for Vh, mean ratio: 0.27 ± 0.065, n= 6 mice; for PCP: 0.423 ± 0.035, n= 8 mice; Mann-Whitney U test: U = 7, p = 0.293); day 34 (for Vh, mean ratio: 0.32 ± 0.0627, n= 4 mice; for PCP: 0.3625 ± 0.030, n= 9 mice; Mann-Whitney U test: U = 12, p = 0.207) and day 40 (for Vh, mean ratio: 0.318 ± 0.071, n= 6 mice; for PCP: 0.318 ± 0.034, n= 9 mice; Mann-Whitney U test: U = 26, p = 0.964). Each dot is the quantification of a single animal.
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    (A) Scheme showing the treatment regime used to study the effect of subchronic PCP on cognition using the T-Maze alternation task; on <t>ASSR</t> using electroencephalography (EEG); on local mPFC network using ex vivo electrophysiology (EPhys) and immunohistochemistry (IHC) of PV; on the long-range inputs from vHPC to mPFC using optogenetics; and on brain networks using functional ultrasound imaging (fUS). Different cohorts of mice were used for each experiment. (B) Percent of spontaneous alternation of vehicle- and PCP treated mice in the T-Maze task at day 21 (for Vh, mean spontaneous alternation: 70.3 ± 3.2 %, n= 9 mice; for PCP: 60.4 ± 8.9%, n= 15 mice; Mann-Whitney U test: U = 31.5, p = 0.03). (C) Heatmaps of phase-lock ratio (left) in 40 Hz ASSR from the mPFC of vehicle- and PCP treated animals and quantifications at day 24 (for Vh, mean ratio: 0.33 ± 0.046, n= 5 mice; for PCP: 0.462 ± 0.029, n= 9 mice; Mann-Whitney U test: U = 8, p = 0.0599) day 31 (for Vh, mean ratio: 0.27 ± 0.065, n= 6 mice; for PCP: 0.423 ± 0.035, n= 8 mice; Mann-Whitney U test: U = 7, p = 0.293); day 34 (for Vh, mean ratio: 0.32 ± 0.0627, n= 4 mice; for PCP: 0.3625 ± 0.030, n= 9 mice; Mann-Whitney U test: U = 12, p = 0.207) and day 40 (for Vh, mean ratio: 0.318 ± 0.071, n= 6 mice; for PCP: 0.318 ± 0.034, n= 9 mice; Mann-Whitney U test: U = 26, p = 0.964). Each dot is the quantification of a single animal.
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    auditory steady state responses (assrs)  (Wolters Kluwer Health)
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    Wolters Kluwer Health auditory steady state responses (assrs)
    (A) Scheme showing the treatment regime used to study the effect of subchronic PCP on cognition using the T-Maze alternation task; on <t>ASSR</t> using electroencephalography (EEG); on local mPFC network using ex vivo electrophysiology (EPhys) and immunohistochemistry (IHC) of PV; on the long-range inputs from vHPC to mPFC using optogenetics; and on brain networks using functional ultrasound imaging (fUS). Different cohorts of mice were used for each experiment. (B) Percent of spontaneous alternation of vehicle- and PCP treated mice in the T-Maze task at day 21 (for Vh, mean spontaneous alternation: 70.3 ± 3.2 %, n= 9 mice; for PCP: 60.4 ± 8.9%, n= 15 mice; Mann-Whitney U test: U = 31.5, p = 0.03). (C) Heatmaps of phase-lock ratio (left) in 40 Hz ASSR from the mPFC of vehicle- and PCP treated animals and quantifications at day 24 (for Vh, mean ratio: 0.33 ± 0.046, n= 5 mice; for PCP: 0.462 ± 0.029, n= 9 mice; Mann-Whitney U test: U = 8, p = 0.0599) day 31 (for Vh, mean ratio: 0.27 ± 0.065, n= 6 mice; for PCP: 0.423 ± 0.035, n= 8 mice; Mann-Whitney U test: U = 7, p = 0.293); day 34 (for Vh, mean ratio: 0.32 ± 0.0627, n= 4 mice; for PCP: 0.3625 ± 0.030, n= 9 mice; Mann-Whitney U test: U = 12, p = 0.207) and day 40 (for Vh, mean ratio: 0.318 ± 0.071, n= 6 mice; for PCP: 0.318 ± 0.034, n= 9 mice; Mann-Whitney U test: U = 26, p = 0.964). Each dot is the quantification of a single animal.
    Auditory Steady State Responses (Assrs), supplied by Wolters Kluwer Health, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    (A) Scheme showing the treatment regime used to study the effect of subchronic PCP on cognition using the T-Maze alternation task; on ASSR using electroencephalography (EEG); on local mPFC network using ex vivo electrophysiology (EPhys) and immunohistochemistry (IHC) of PV; on the long-range inputs from vHPC to mPFC using optogenetics; and on brain networks using functional ultrasound imaging (fUS). Different cohorts of mice were used for each experiment. (B) Percent of spontaneous alternation of vehicle- and PCP treated mice in the T-Maze task at day 21 (for Vh, mean spontaneous alternation: 70.3 ± 3.2 %, n= 9 mice; for PCP: 60.4 ± 8.9%, n= 15 mice; Mann-Whitney U test: U = 31.5, p = 0.03). (C) Heatmaps of phase-lock ratio (left) in 40 Hz ASSR from the mPFC of vehicle- and PCP treated animals and quantifications at day 24 (for Vh, mean ratio: 0.33 ± 0.046, n= 5 mice; for PCP: 0.462 ± 0.029, n= 9 mice; Mann-Whitney U test: U = 8, p = 0.0599) day 31 (for Vh, mean ratio: 0.27 ± 0.065, n= 6 mice; for PCP: 0.423 ± 0.035, n= 8 mice; Mann-Whitney U test: U = 7, p = 0.293); day 34 (for Vh, mean ratio: 0.32 ± 0.0627, n= 4 mice; for PCP: 0.3625 ± 0.030, n= 9 mice; Mann-Whitney U test: U = 12, p = 0.207) and day 40 (for Vh, mean ratio: 0.318 ± 0.071, n= 6 mice; for PCP: 0.318 ± 0.034, n= 9 mice; Mann-Whitney U test: U = 26, p = 0.964). Each dot is the quantification of a single animal.

    Journal: bioRxiv

    Article Title: Long-term adaptation of prefrontal circuits in a mouse model of NMDAR hypofunction

    doi: 10.1101/2024.02.15.580421

    Figure Lengend Snippet: (A) Scheme showing the treatment regime used to study the effect of subchronic PCP on cognition using the T-Maze alternation task; on ASSR using electroencephalography (EEG); on local mPFC network using ex vivo electrophysiology (EPhys) and immunohistochemistry (IHC) of PV; on the long-range inputs from vHPC to mPFC using optogenetics; and on brain networks using functional ultrasound imaging (fUS). Different cohorts of mice were used for each experiment. (B) Percent of spontaneous alternation of vehicle- and PCP treated mice in the T-Maze task at day 21 (for Vh, mean spontaneous alternation: 70.3 ± 3.2 %, n= 9 mice; for PCP: 60.4 ± 8.9%, n= 15 mice; Mann-Whitney U test: U = 31.5, p = 0.03). (C) Heatmaps of phase-lock ratio (left) in 40 Hz ASSR from the mPFC of vehicle- and PCP treated animals and quantifications at day 24 (for Vh, mean ratio: 0.33 ± 0.046, n= 5 mice; for PCP: 0.462 ± 0.029, n= 9 mice; Mann-Whitney U test: U = 8, p = 0.0599) day 31 (for Vh, mean ratio: 0.27 ± 0.065, n= 6 mice; for PCP: 0.423 ± 0.035, n= 8 mice; Mann-Whitney U test: U = 7, p = 0.293); day 34 (for Vh, mean ratio: 0.32 ± 0.0627, n= 4 mice; for PCP: 0.3625 ± 0.030, n= 9 mice; Mann-Whitney U test: U = 12, p = 0.207) and day 40 (for Vh, mean ratio: 0.318 ± 0.071, n= 6 mice; for PCP: 0.318 ± 0.034, n= 9 mice; Mann-Whitney U test: U = 26, p = 0.964). Each dot is the quantification of a single animal.

    Article Snippet: Wireless recording of 40Hz auditory steady-state response (ASSR) was established using the Neurologger system (TSE Systems) and auditory stimuli generated with an audio generator (MED Associates Inc.).

    Techniques: Ex Vivo, Immunohistochemistry, Optogenetics, Functional Assay, Imaging, MANN-WHITNEY