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surface electrodes  (ADInstruments)


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    Structured Review

    ADInstruments surface electrodes
    Surface Electrodes, supplied by ADInstruments, used in various techniques. Bioz Stars score: 93/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/surface electrodes/product/ADInstruments
    Average 93 stars, based on 9 article reviews
    surface electrodes - by Bioz Stars, 2026-05
    93/100 stars

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    Data Sciences International surface electrocardiogram (ecg) p3 plus
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    Transplantation of gut microbiota from aged mice increases susceptibility to arrhythmia (A) Sample <t>ECG</t> traces of four different types of arrhythmic events: ventricular premature beats (VPB), ventricular tachycardia (VT), atrial fibrillation (AF), and atrioventricular block (AVB). (B) Summary the inducibility of VPB, VT, AF, and AVB in young and aged mice. Numbers in parentheses indicate the number of mice that were induced into VPB, VT, AF, AVB following ISO treated ( n = 6/per group). Data analyzed by Fischer’s exact test. (C) Differences in heart rates, PR intervals, QRS intervals, R amplitude, P duration and P amplitude among young-young FMT, young-aged FMT, aged-aged FMT and aged-young FMT mice ( n = 6/per group). Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (D) Representative western blot and quantification of Cx43, Cx40, Nav1.5, Cav1.2, Serca-2A, Kv4.2, IL-6, IL-10, IL-1β, TNF-α, TGF-β, α-SMA, GAPDH in ventricular and atrial tissue of young-young FMT, young-aged FMT, aged-aged FMT and aged-young FMT mice ( n = 6/per group). GAPDH was used for internal normalization. Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (E) Representative micrographs of Cx43 signal in ventricular and Cx40 in stained atrial sections visualized ( n = 6/per group). Cx43 indicates Connexin 43; Cx40, Connexin 40; ISO, isoproterenol; IL-6, Interleukin-6; TNF-α, tumor necrosis factor-α; TGF-β, transforming growth factor β.
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    Respiratory rate (RR) estimation in spontaneously breathing humans. ( A ) RR estimates, in breaths per minute (bpm), during 3 levels of exercise in one subject. Algorithm-estimated RRs (estimated, blue) are compared with RR measured from the subject using the respiratory inductive plethysmography based Hexoskin monitor (expected, red) while performing three consecutive tasks: (1) resting, standing upright on a treadmill (Int 1); (2) walking on the treadmill at a moderate speed (1.2 m/s) (int 2); and (3) walking on the treadmill with 15% track inclination at the moderate speed (Int 3). ( B ) Summary results of algorithm-estimated and reference RRs (blue and red, respectively) during each subject-task interval. The data are from seven subjects, each performing either or all the three levels of exercise described above (subject-tasks), and presented in order of increasing average expected RR values. ( C ) The absolute errors (black) and relative errors (gray) of the algorithmic RR estimations across the subject-task intervals described above. Equivalence testing revealed that the expected and estimated RRs were the same ( p < 0.0001) for all subject-task intervals. ( D ) A comparison of the <t>ECG</t> cycle-to-cycle estimated and expected RR for all subjects and tasks with the indicated R 2 value (0.9092) and low root mean square error (RMSE, 2.2bpm) support a close linear relationship between the values. ( E ) Absolute error (bpm) and ( F ) relative error (%) distributions across all subjects.
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    Transplantation of gut microbiota from aged mice increases susceptibility to arrhythmia (A) Sample ECG traces of four different types of arrhythmic events: ventricular premature beats (VPB), ventricular tachycardia (VT), atrial fibrillation (AF), and atrioventricular block (AVB). (B) Summary the inducibility of VPB, VT, AF, and AVB in young and aged mice. Numbers in parentheses indicate the number of mice that were induced into VPB, VT, AF, AVB following ISO treated ( n = 6/per group). Data analyzed by Fischer’s exact test. (C) Differences in heart rates, PR intervals, QRS intervals, R amplitude, P duration and P amplitude among young-young FMT, young-aged FMT, aged-aged FMT and aged-young FMT mice ( n = 6/per group). Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (D) Representative western blot and quantification of Cx43, Cx40, Nav1.5, Cav1.2, Serca-2A, Kv4.2, IL-6, IL-10, IL-1β, TNF-α, TGF-β, α-SMA, GAPDH in ventricular and atrial tissue of young-young FMT, young-aged FMT, aged-aged FMT and aged-young FMT mice ( n = 6/per group). GAPDH was used for internal normalization. Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (E) Representative micrographs of Cx43 signal in ventricular and Cx40 in stained atrial sections visualized ( n = 6/per group). Cx43 indicates Connexin 43; Cx40, Connexin 40; ISO, isoproterenol; IL-6, Interleukin-6; TNF-α, tumor necrosis factor-α; TGF-β, transforming growth factor β.

    Journal: iScience

    Article Title: Aged gut microbiota promotes arrhythmia susceptibility via oxidative stress

    doi: 10.1016/j.isci.2024.110888

    Figure Lengend Snippet: Transplantation of gut microbiota from aged mice increases susceptibility to arrhythmia (A) Sample ECG traces of four different types of arrhythmic events: ventricular premature beats (VPB), ventricular tachycardia (VT), atrial fibrillation (AF), and atrioventricular block (AVB). (B) Summary the inducibility of VPB, VT, AF, and AVB in young and aged mice. Numbers in parentheses indicate the number of mice that were induced into VPB, VT, AF, AVB following ISO treated ( n = 6/per group). Data analyzed by Fischer’s exact test. (C) Differences in heart rates, PR intervals, QRS intervals, R amplitude, P duration and P amplitude among young-young FMT, young-aged FMT, aged-aged FMT and aged-young FMT mice ( n = 6/per group). Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (D) Representative western blot and quantification of Cx43, Cx40, Nav1.5, Cav1.2, Serca-2A, Kv4.2, IL-6, IL-10, IL-1β, TNF-α, TGF-β, α-SMA, GAPDH in ventricular and atrial tissue of young-young FMT, young-aged FMT, aged-aged FMT and aged-young FMT mice ( n = 6/per group). GAPDH was used for internal normalization. Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (E) Representative micrographs of Cx43 signal in ventricular and Cx40 in stained atrial sections visualized ( n = 6/per group). Cx43 indicates Connexin 43; Cx40, Connexin 40; ISO, isoproterenol; IL-6, Interleukin-6; TNF-α, tumor necrosis factor-α; TGF-β, transforming growth factor β.

    Article Snippet: Surface electrocardiogram (ECG) was monitored by P3 plus (Data Sciences International), 1.5% isoflurane-oxygen mixture was anesthetized, and subcutaneous platinum electrode was placed on lead II.

    Techniques: Transplantation Assay, Blocking Assay, Western Blot, Staining

    Vitexin improved aged related arrhythmia through OLA1-Nrf2 signaling pathway (A) Experimental design for testing the anti-aging effect of vitexin on aged mice induced by 150 mg kg D-gal. (B) Sample ECG traces of three different types of arrhythmic events: ventricular premature beats (VPB), atrial fibrillation (AF), and atrioventricular block (AVB). (C) Summary of inducibility of VPB, AF, and AVB in vehicle, and vitexin treated aged mice. Numbers in parentheses indicate the number of mice that were induced into VPB, AF, AVB following ISO treated ( n = 6/per group). Data analyzed by Fischer’s exact test. And differences in heart rates, P-R intervals, QRS intervals, and R amplitude among different group ( n = 6/per group). Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (D) The examples of HE, Sirius red staining in the ventricle and atria from different group of mice ( n = 6/per group). Scale bar, 100 μm. Viteixn attenuated fibrosis in aged mice measured by Sirius red staining. Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (E and I) Cardiac, serum, colon MDA, SOD and GSH-px levels were quantified using commercial assay kits. ( n = 6/per group). Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (F) Representative western blot and quantification of Cx43, Nav1.5, Cav1.2, Serca-2A, Kv4.2, α-SMA, OLA1, Nrf2, GAPDH in ventricle and atria in the four groups ( n = 6/per group). GAPDH was used for internal normalization. Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (G) Experimental design for testing the anti-aging effect of Nrf2 activator and inhibitor on aged mice induced by 150 mg kg D-gal. Summary of inducibility of VPB, AF, and AVB in vitexin, DMF, ML385 treated aged mice. Numbers in parentheses indicate the number of mice that were induced into VPB, AF, AVB following ISO treated ( n = 6/per group). Data analyzed by Fischer’s exact test. (H) The examples of HE, Sirius red staining in the ventricle from different group of mice ( n = 6/per group). Scale bar, 100 μm. Viteixn and DMF attenuated fibrosis in aged mice measured by Sirius red staining. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. Serum levels were quantified using commercial assay kits. ( n = 6/per group). Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (J) Representative western blot and quantification of Cx43, Nav1.5, Cav1.2, Serca-2A, Kv4.2, α-SMA, OLA1, Nrf2, and GAPDH in ventricle in the four groups ( n = 6/per group). GAPDH was used for internal normalization. Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.

    Journal: iScience

    Article Title: Aged gut microbiota promotes arrhythmia susceptibility via oxidative stress

    doi: 10.1016/j.isci.2024.110888

    Figure Lengend Snippet: Vitexin improved aged related arrhythmia through OLA1-Nrf2 signaling pathway (A) Experimental design for testing the anti-aging effect of vitexin on aged mice induced by 150 mg kg D-gal. (B) Sample ECG traces of three different types of arrhythmic events: ventricular premature beats (VPB), atrial fibrillation (AF), and atrioventricular block (AVB). (C) Summary of inducibility of VPB, AF, and AVB in vehicle, and vitexin treated aged mice. Numbers in parentheses indicate the number of mice that were induced into VPB, AF, AVB following ISO treated ( n = 6/per group). Data analyzed by Fischer’s exact test. And differences in heart rates, P-R intervals, QRS intervals, and R amplitude among different group ( n = 6/per group). Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (D) The examples of HE, Sirius red staining in the ventricle and atria from different group of mice ( n = 6/per group). Scale bar, 100 μm. Viteixn attenuated fibrosis in aged mice measured by Sirius red staining. Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (E and I) Cardiac, serum, colon MDA, SOD and GSH-px levels were quantified using commercial assay kits. ( n = 6/per group). Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (F) Representative western blot and quantification of Cx43, Nav1.5, Cav1.2, Serca-2A, Kv4.2, α-SMA, OLA1, Nrf2, GAPDH in ventricle and atria in the four groups ( n = 6/per group). GAPDH was used for internal normalization. Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (G) Experimental design for testing the anti-aging effect of Nrf2 activator and inhibitor on aged mice induced by 150 mg kg D-gal. Summary of inducibility of VPB, AF, and AVB in vitexin, DMF, ML385 treated aged mice. Numbers in parentheses indicate the number of mice that were induced into VPB, AF, AVB following ISO treated ( n = 6/per group). Data analyzed by Fischer’s exact test. (H) The examples of HE, Sirius red staining in the ventricle from different group of mice ( n = 6/per group). Scale bar, 100 μm. Viteixn and DMF attenuated fibrosis in aged mice measured by Sirius red staining. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. Serum levels were quantified using commercial assay kits. ( n = 6/per group). Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. (J) Representative western blot and quantification of Cx43, Nav1.5, Cav1.2, Serca-2A, Kv4.2, α-SMA, OLA1, Nrf2, and GAPDH in ventricle in the four groups ( n = 6/per group). GAPDH was used for internal normalization. Data are presented as the mean ± SD. Data analyzed by one-way ANOVA with Tukey’s post-hoc test. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.

    Article Snippet: Surface electrocardiogram (ECG) was monitored by P3 plus (Data Sciences International), 1.5% isoflurane-oxygen mixture was anesthetized, and subcutaneous platinum electrode was placed on lead II.

    Techniques: Blocking Assay, Staining, Western Blot

    Respiratory rate (RR) estimation in spontaneously breathing humans. ( A ) RR estimates, in breaths per minute (bpm), during 3 levels of exercise in one subject. Algorithm-estimated RRs (estimated, blue) are compared with RR measured from the subject using the respiratory inductive plethysmography based Hexoskin monitor (expected, red) while performing three consecutive tasks: (1) resting, standing upright on a treadmill (Int 1); (2) walking on the treadmill at a moderate speed (1.2 m/s) (int 2); and (3) walking on the treadmill with 15% track inclination at the moderate speed (Int 3). ( B ) Summary results of algorithm-estimated and reference RRs (blue and red, respectively) during each subject-task interval. The data are from seven subjects, each performing either or all the three levels of exercise described above (subject-tasks), and presented in order of increasing average expected RR values. ( C ) The absolute errors (black) and relative errors (gray) of the algorithmic RR estimations across the subject-task intervals described above. Equivalence testing revealed that the expected and estimated RRs were the same ( p < 0.0001) for all subject-task intervals. ( D ) A comparison of the ECG cycle-to-cycle estimated and expected RR for all subjects and tasks with the indicated R 2 value (0.9092) and low root mean square error (RMSE, 2.2bpm) support a close linear relationship between the values. ( E ) Absolute error (bpm) and ( F ) relative error (%) distributions across all subjects.

    Journal: Scientific Reports

    Article Title: Open-source software for respiratory rate estimation using single-lead electrocardiograms

    doi: 10.1038/s41598-023-50470-0

    Figure Lengend Snippet: Respiratory rate (RR) estimation in spontaneously breathing humans. ( A ) RR estimates, in breaths per minute (bpm), during 3 levels of exercise in one subject. Algorithm-estimated RRs (estimated, blue) are compared with RR measured from the subject using the respiratory inductive plethysmography based Hexoskin monitor (expected, red) while performing three consecutive tasks: (1) resting, standing upright on a treadmill (Int 1); (2) walking on the treadmill at a moderate speed (1.2 m/s) (int 2); and (3) walking on the treadmill with 15% track inclination at the moderate speed (Int 3). ( B ) Summary results of algorithm-estimated and reference RRs (blue and red, respectively) during each subject-task interval. The data are from seven subjects, each performing either or all the three levels of exercise described above (subject-tasks), and presented in order of increasing average expected RR values. ( C ) The absolute errors (black) and relative errors (gray) of the algorithmic RR estimations across the subject-task intervals described above. Equivalence testing revealed that the expected and estimated RRs were the same ( p < 0.0001) for all subject-task intervals. ( D ) A comparison of the ECG cycle-to-cycle estimated and expected RR for all subjects and tasks with the indicated R 2 value (0.9092) and low root mean square error (RMSE, 2.2bpm) support a close linear relationship between the values. ( E ) Absolute error (bpm) and ( F ) relative error (%) distributions across all subjects.

    Article Snippet: Single-lead body surface ECG signals were obtained during the procedure and 90 min after coil placement using the AD Instruments PowerLab 4/35 system with Labchart 8 software.

    Techniques: Comparison

    Block diagram of respiration rate estimation algorithm. Raw single-lead ECG data are filtered (panels a and b ), R-peaks are detected (red symbols, panel c ), R-peak intervals are determined, QRS complexes are extracted (panel d ) and their root mean square amplitude (RMS) values are calculated (panel e ), a power spectrum is generated for a moving window of 16 QRS RMS values incremented one value at a time (panel f ), and its peak frequency and the R-peak interval data within the window are used to calculate the respiratory rate (RR) using the equation shown.

    Journal: Scientific Reports

    Article Title: Open-source software for respiratory rate estimation using single-lead electrocardiograms

    doi: 10.1038/s41598-023-50470-0

    Figure Lengend Snippet: Block diagram of respiration rate estimation algorithm. Raw single-lead ECG data are filtered (panels a and b ), R-peaks are detected (red symbols, panel c ), R-peak intervals are determined, QRS complexes are extracted (panel d ) and their root mean square amplitude (RMS) values are calculated (panel e ), a power spectrum is generated for a moving window of 16 QRS RMS values incremented one value at a time (panel f ), and its peak frequency and the R-peak interval data within the window are used to calculate the respiratory rate (RR) using the equation shown.

    Article Snippet: Single-lead body surface ECG signals were obtained during the procedure and 90 min after coil placement using the AD Instruments PowerLab 4/35 system with Labchart 8 software.

    Techniques: Blocking Assay, Generated