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64-channel multielectrode array (mea) recording system  (Alpha MED Scientific)


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    Alpha MED Scientific 64-channel multielectrode array (mea) recording system
    64 Channel Multielectrode Array (Mea) Recording System, supplied by Alpha MED Scientific, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/64-channel+multielectrode+recording+system/64+channel+multielectrode+system/bio_rxiv__2024__10__14__618205-236-1-7
    Average 90 stars, based on 1 article reviews
    64-channel multielectrode array (mea) recording system - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Brain-derived neurotrophic factor produced long-term synaptic enhancement in the anterior cingulate cortex of adult mice.
    Article Snippet: In the present study, we aimed to study the effect of BDNF on synaptic transmission in ACC by using a 64-channel multielectrode (MED64) recording system.

    Article Title: Diabetic hyperglycemia aggravates seizures and status epilepticus-induced hippocampal damage.
    Article Snippet: Epileptic seizures in diabetic hyperglycemia (DH) are not uncommon.. This study aimed to determine the acute behavioral, pathological, and electrophysiological effects of status epilepticus (SE) on diabetic animals.. Adult male Sprague-Dawley rats were first divided into groups with and without streptozotocin (STZ)-induced diabetes, and then into treatment groups given a normal saline (NS) (STZ-only and NS-only) or a lithium-pilocarpine injection to induce status epilepticus (STZ ?



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    Changed presynaptic transmitter release probably within aIC of observer and demonstrator mice. (A) Left: schematic diagram showing location of the <t>MED64</t> probe on the coronal IC slice; Right: light microscopy photograph showing relative location of aIC within the probe; (B) Spatial distribution of extracellular field potential induced by electrical stimulation on channel 45 (marked as red circle) in layers VI of aIC; (C,D) Input–output curve of fEPSP slope (%) vs. stimulus intensity (mA) in the slice among naïve ( n = 4 slices of 3 mice), observer ( n = 4 slices of 3 mice), and demonstrator ( n = 7 slices of 5 mice) in the superficial (C) and in the deep layers (D) of aIC; (E,F) Example traces of paired-pulse facilitation (PPF) with an interval of 25 ms recorded in the superficial (E) and deep layers (F) of aIC; (G,H) The paired-pulse ratios (slope of fEPSP2/slope of fEPSP1) recorded with intervals of 25, 50, 75, and 100 ms in superficial (G) and deep layers (H) of aIC; Data are shown as mean ± SEM (PPF: Naïve n = 4 slices of 3 mice, observer n = 7 slices of 6 mice, and demonstrator n = 4 slices of 4 mice) and compared by two-way ANOVA analysis followed by Tukey’s multiple comparisons test, * p < 0.05, vs. naïve.
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    Changed presynaptic transmitter release probably within aIC of observer and demonstrator mice. (A) Left: schematic diagram showing location of the <t>MED64</t> probe on the coronal IC slice; Right: light microscopy photograph showing relative location of aIC within the probe; (B) Spatial distribution of extracellular field potential induced by electrical stimulation on channel 45 (marked as red circle) in layers VI of aIC; (C,D) Input–output curve of fEPSP slope (%) vs. stimulus intensity (mA) in the slice among naïve ( n = 4 slices of 3 mice), observer ( n = 4 slices of 3 mice), and demonstrator ( n = 7 slices of 5 mice) in the superficial (C) and in the deep layers (D) of aIC; (E,F) Example traces of paired-pulse facilitation (PPF) with an interval of 25 ms recorded in the superficial (E) and deep layers (F) of aIC; (G,H) The paired-pulse ratios (slope of fEPSP2/slope of fEPSP1) recorded with intervals of 25, 50, 75, and 100 ms in superficial (G) and deep layers (H) of aIC; Data are shown as mean ± SEM (PPF: Naïve n = 4 slices of 3 mice, observer n = 7 slices of 6 mice, and demonstrator n = 4 slices of 4 mice) and compared by two-way ANOVA analysis followed by Tukey’s multiple comparisons test, * p < 0.05, vs. naïve.
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    Changed presynaptic transmitter release probably within aIC of observer and demonstrator mice. (A) Left: schematic diagram showing location of the <t>MED64</t> probe on the coronal IC slice; Right: light microscopy photograph showing relative location of aIC within the probe; (B) Spatial distribution of extracellular field potential induced by electrical stimulation on channel 45 (marked as red circle) in layers VI of aIC; (C,D) Input–output curve of fEPSP slope (%) vs. stimulus intensity (mA) in the slice among naïve ( n = 4 slices of 3 mice), observer ( n = 4 slices of 3 mice), and demonstrator ( n = 7 slices of 5 mice) in the superficial (C) and in the deep layers (D) of aIC; (E,F) Example traces of paired-pulse facilitation (PPF) with an interval of 25 ms recorded in the superficial (E) and deep layers (F) of aIC; (G,H) The paired-pulse ratios (slope of fEPSP2/slope of fEPSP1) recorded with intervals of 25, 50, 75, and 100 ms in superficial (G) and deep layers (H) of aIC; Data are shown as mean ± SEM (PPF: Naïve n = 4 slices of 3 mice, observer n = 7 slices of 6 mice, and demonstrator n = 4 slices of 4 mice) and compared by two-way ANOVA analysis followed by Tukey’s multiple comparisons test, * p < 0.05, vs. naïve.
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    Changed presynaptic transmitter release probably within aIC of observer and demonstrator mice. (A) Left: schematic diagram showing location of the MED64 probe on the coronal IC slice; Right: light microscopy photograph showing relative location of aIC within the probe; (B) Spatial distribution of extracellular field potential induced by electrical stimulation on channel 45 (marked as red circle) in layers VI of aIC; (C,D) Input–output curve of fEPSP slope (%) vs. stimulus intensity (mA) in the slice among naïve ( n = 4 slices of 3 mice), observer ( n = 4 slices of 3 mice), and demonstrator ( n = 7 slices of 5 mice) in the superficial (C) and in the deep layers (D) of aIC; (E,F) Example traces of paired-pulse facilitation (PPF) with an interval of 25 ms recorded in the superficial (E) and deep layers (F) of aIC; (G,H) The paired-pulse ratios (slope of fEPSP2/slope of fEPSP1) recorded with intervals of 25, 50, 75, and 100 ms in superficial (G) and deep layers (H) of aIC; Data are shown as mean ± SEM (PPF: Naïve n = 4 slices of 3 mice, observer n = 7 slices of 6 mice, and demonstrator n = 4 slices of 4 mice) and compared by two-way ANOVA analysis followed by Tukey’s multiple comparisons test, * p < 0.05, vs. naïve.

    Journal: Frontiers in Synaptic Neuroscience

    Article Title: Different Synaptic Plasticity After Physiological and Psychological Stress in the Anterior Insular Cortex in an Observational Fear Mouse Model

    doi: 10.3389/fnsyn.2022.851015

    Figure Lengend Snippet: Changed presynaptic transmitter release probably within aIC of observer and demonstrator mice. (A) Left: schematic diagram showing location of the MED64 probe on the coronal IC slice; Right: light microscopy photograph showing relative location of aIC within the probe; (B) Spatial distribution of extracellular field potential induced by electrical stimulation on channel 45 (marked as red circle) in layers VI of aIC; (C,D) Input–output curve of fEPSP slope (%) vs. stimulus intensity (mA) in the slice among naïve ( n = 4 slices of 3 mice), observer ( n = 4 slices of 3 mice), and demonstrator ( n = 7 slices of 5 mice) in the superficial (C) and in the deep layers (D) of aIC; (E,F) Example traces of paired-pulse facilitation (PPF) with an interval of 25 ms recorded in the superficial (E) and deep layers (F) of aIC; (G,H) The paired-pulse ratios (slope of fEPSP2/slope of fEPSP1) recorded with intervals of 25, 50, 75, and 100 ms in superficial (G) and deep layers (H) of aIC; Data are shown as mean ± SEM (PPF: Naïve n = 4 slices of 3 mice, observer n = 7 slices of 6 mice, and demonstrator n = 4 slices of 4 mice) and compared by two-way ANOVA analysis followed by Tukey’s multiple comparisons test, * p < 0.05, vs. naïve.

    Article Snippet: The 64-channel multielectrode array recording system (MED64; Panasonic Alpha-Med Sciences, Osaka, Japan) was used for extracellular field potential recordings.

    Techniques: Light Microscopy