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physiological signal acquisition system mp160  (BIOPAC)

 
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    Structured Review

    BIOPAC physiological signal acquisition system mp160
    <t>Physiological</t> and biochemical analyses after HF model establishment. (A) Ejection fraction (EF) and fractional shortening (FS) were analyzed via ultrasonography (n = 10). (B) The maximum rate of rising/declining LV intraventricular pressure (±dp/dt max), left ventricular end systolic pressure (LVSP) and left ventricular end diastolic pressure (LVEDP) were analyzed via hemodynamic analyses (n = 10). (C) Serum B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP) were measured by ELISA. * p < 0.05, ** p < 0.01 and *** p < 0.001 vs. the sham group (n = 10). (D) Representative images of cardiac tissue sections following H&E staining. (E) Representative images of cardiac tissue sections following Masson’s trichrome staining.
    Physiological Signal Acquisition System Mp160, supplied by BIOPAC, 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/result/physiological signal acquisition system mp160/product/BIOPAC
    Average 90 stars, based on 1 article reviews
    physiological signal acquisition system mp160 - by Bioz Stars, 2026-02
    90/100 stars

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    1) Product Images from "Whole-body mass spectrometry imaging reveals the systemic metabolic disorder and catecholamines biosynthesis alteration on heart-gut axis in heart failure rat"

    Article Title: Whole-body mass spectrometry imaging reveals the systemic metabolic disorder and catecholamines biosynthesis alteration on heart-gut axis in heart failure rat

    Journal: Journal of Advanced Research

    doi: 10.1016/j.jare.2024.09.001

    Physiological and biochemical analyses after HF model establishment. (A) Ejection fraction (EF) and fractional shortening (FS) were analyzed via ultrasonography (n = 10). (B) The maximum rate of rising/declining LV intraventricular pressure (±dp/dt max), left ventricular end systolic pressure (LVSP) and left ventricular end diastolic pressure (LVEDP) were analyzed via hemodynamic analyses (n = 10). (C) Serum B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP) were measured by ELISA. * p < 0.05, ** p < 0.01 and *** p < 0.001 vs. the sham group (n = 10). (D) Representative images of cardiac tissue sections following H&E staining. (E) Representative images of cardiac tissue sections following Masson’s trichrome staining.
    Figure Legend Snippet: Physiological and biochemical analyses after HF model establishment. (A) Ejection fraction (EF) and fractional shortening (FS) were analyzed via ultrasonography (n = 10). (B) The maximum rate of rising/declining LV intraventricular pressure (±dp/dt max), left ventricular end systolic pressure (LVSP) and left ventricular end diastolic pressure (LVEDP) were analyzed via hemodynamic analyses (n = 10). (C) Serum B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP) were measured by ELISA. * p < 0.05, ** p < 0.01 and *** p < 0.001 vs. the sham group (n = 10). (D) Representative images of cardiac tissue sections following H&E staining. (E) Representative images of cardiac tissue sections following Masson’s trichrome staining.

    Techniques Used: Enzyme-linked Immunosorbent Assay, Staining

    Physiological and biochemical analyses of validation experiments. (A) Ejection fraction (EF), fractional shortening (FS), left ventricular internal dimension systole (LVIDs) and left ventricular end-systolic volume (LVESV) were analyzed via ultrasonography in Sham (n = 10), Sham-NE (n = 6), Model (n = 10), Model-NE (n = 9) and MET groups (n = 11). (B) The maximum rate of rising/declining LV intraventricular pressure (±dp/dt max), LV systolic pressure (LVSP) and left ventricular end diastolic pressure (LVEDP) were analyzed via hemodynamic analyses in Sham (n = 10), Sham-NE (n = 6), Model (n = 10), Model-NE (n = 9) and MET groups (n = 11). (C) Serum B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP), lipopolysaccharide (LPS) and diamine oxidase (DAO) were measured by ELISA in Sham (n = 10), Sham-NE (n = 6), Model (n = 10), Model-NE (n = 9) and MET groups (n = 11). (D) Representative images of cardiac tissue sections following H&E or Masson’s trichrome staining. (E) Representative images of colonic tissue sections following H&E staining. (F) Relative abundance of s_Turicibacter_sanguinis in Sham, Sham-NE, Model, Model-NE and MET groups. * p < 0.05, ** p < 0.01 and *** p < 0.001 vs. the sham group, # p < 0.05, ## p < 0.01 and ### p < 0.001 vs. the model group.
    Figure Legend Snippet: Physiological and biochemical analyses of validation experiments. (A) Ejection fraction (EF), fractional shortening (FS), left ventricular internal dimension systole (LVIDs) and left ventricular end-systolic volume (LVESV) were analyzed via ultrasonography in Sham (n = 10), Sham-NE (n = 6), Model (n = 10), Model-NE (n = 9) and MET groups (n = 11). (B) The maximum rate of rising/declining LV intraventricular pressure (±dp/dt max), LV systolic pressure (LVSP) and left ventricular end diastolic pressure (LVEDP) were analyzed via hemodynamic analyses in Sham (n = 10), Sham-NE (n = 6), Model (n = 10), Model-NE (n = 9) and MET groups (n = 11). (C) Serum B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP), lipopolysaccharide (LPS) and diamine oxidase (DAO) were measured by ELISA in Sham (n = 10), Sham-NE (n = 6), Model (n = 10), Model-NE (n = 9) and MET groups (n = 11). (D) Representative images of cardiac tissue sections following H&E or Masson’s trichrome staining. (E) Representative images of colonic tissue sections following H&E staining. (F) Relative abundance of s_Turicibacter_sanguinis in Sham, Sham-NE, Model, Model-NE and MET groups. * p < 0.05, ** p < 0.01 and *** p < 0.001 vs. the sham group, # p < 0.05, ## p < 0.01 and ### p < 0.001 vs. the model group.

    Techniques Used: Biomarker Discovery, Enzyme-linked Immunosorbent Assay, Staining



    Similar Products

    physiological signal acquisition system mp160  (BIOPAC)
    90
    BIOPAC physiological signal acquisition system mp160
    <t>Physiological</t> and biochemical analyses after HF model establishment. (A) Ejection fraction (EF) and fractional shortening (FS) were analyzed via ultrasonography (n = 10). (B) The maximum rate of rising/declining LV intraventricular pressure (±dp/dt max), left ventricular end systolic pressure (LVSP) and left ventricular end diastolic pressure (LVEDP) were analyzed via hemodynamic analyses (n = 10). (C) Serum B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP) were measured by ELISA. * p < 0.05, ** p < 0.01 and *** p < 0.001 vs. the sham group (n = 10). (D) Representative images of cardiac tissue sections following H&E staining. (E) Representative images of cardiac tissue sections following Masson’s trichrome staining.
    Physiological Signal Acquisition System Mp160, supplied by BIOPAC, 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/result/physiological signal acquisition system mp160/product/BIOPAC
    Average 90 stars, based on 1 article reviews
    physiological signal acquisition system mp160 - by Bioz Stars, 2026-02
    90/100 stars
    		  Buy from Supplier
    physiological signal acquisition device biopac mp160  (BIOPAC)
    90
    BIOPAC physiological signal acquisition device biopac mp160
    <t>Physiological</t> and biochemical analyses after HF model establishment. (A) Ejection fraction (EF) and fractional shortening (FS) were analyzed via ultrasonography (n = 10). (B) The maximum rate of rising/declining LV intraventricular pressure (±dp/dt max), left ventricular end systolic pressure (LVSP) and left ventricular end diastolic pressure (LVEDP) were analyzed via hemodynamic analyses (n = 10). (C) Serum B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP) were measured by ELISA. * p < 0.05, ** p < 0.01 and *** p < 0.001 vs. the sham group (n = 10). (D) Representative images of cardiac tissue sections following H&E staining. (E) Representative images of cardiac tissue sections following Masson’s trichrome staining.
    Physiological Signal Acquisition Device Biopac Mp160, supplied by BIOPAC, 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/result/physiological signal acquisition device biopac mp160/product/BIOPAC
    Average 90 stars, based on 1 article reviews
    physiological signal acquisition device biopac mp160 - by Bioz Stars, 2026-02
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Physiological and biochemical analyses after HF model establishment. (A) Ejection fraction (EF) and fractional shortening (FS) were analyzed via ultrasonography (n = 10). (B) The maximum rate of rising/declining LV intraventricular pressure (±dp/dt max), left ventricular end systolic pressure (LVSP) and left ventricular end diastolic pressure (LVEDP) were analyzed via hemodynamic analyses (n = 10). (C) Serum B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP) were measured by ELISA. * p < 0.05, ** p < 0.01 and *** p < 0.001 vs. the sham group (n = 10). (D) Representative images of cardiac tissue sections following H&E staining. (E) Representative images of cardiac tissue sections following Masson’s trichrome staining.

    Journal: Journal of Advanced Research

    Article Title: Whole-body mass spectrometry imaging reveals the systemic metabolic disorder and catecholamines biosynthesis alteration on heart-gut axis in heart failure rat

    doi: 10.1016/j.jare.2024.09.001

    Figure Lengend Snippet: Physiological and biochemical analyses after HF model establishment. (A) Ejection fraction (EF) and fractional shortening (FS) were analyzed via ultrasonography (n = 10). (B) The maximum rate of rising/declining LV intraventricular pressure (±dp/dt max), left ventricular end systolic pressure (LVSP) and left ventricular end diastolic pressure (LVEDP) were analyzed via hemodynamic analyses (n = 10). (C) Serum B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP) were measured by ELISA. * p < 0.05, ** p < 0.01 and *** p < 0.001 vs. the sham group (n = 10). (D) Representative images of cardiac tissue sections following H&E staining. (E) Representative images of cardiac tissue sections following Masson’s trichrome staining.

    Article Snippet: Following weighing and anesthetization, a Millar catheter (SPR-320NR, Millar,USA) was introduced into the left ventricle, and hemodynamic indices were simultaneously recorded using a physiological signal acquisition system (MP160, BIOPAC System, USA).

    Techniques: Enzyme-linked Immunosorbent Assay, Staining

    Physiological and biochemical analyses of validation experiments. (A) Ejection fraction (EF), fractional shortening (FS), left ventricular internal dimension systole (LVIDs) and left ventricular end-systolic volume (LVESV) were analyzed via ultrasonography in Sham (n = 10), Sham-NE (n = 6), Model (n = 10), Model-NE (n = 9) and MET groups (n = 11). (B) The maximum rate of rising/declining LV intraventricular pressure (±dp/dt max), LV systolic pressure (LVSP) and left ventricular end diastolic pressure (LVEDP) were analyzed via hemodynamic analyses in Sham (n = 10), Sham-NE (n = 6), Model (n = 10), Model-NE (n = 9) and MET groups (n = 11). (C) Serum B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP), lipopolysaccharide (LPS) and diamine oxidase (DAO) were measured by ELISA in Sham (n = 10), Sham-NE (n = 6), Model (n = 10), Model-NE (n = 9) and MET groups (n = 11). (D) Representative images of cardiac tissue sections following H&E or Masson’s trichrome staining. (E) Representative images of colonic tissue sections following H&E staining. (F) Relative abundance of s_Turicibacter_sanguinis in Sham, Sham-NE, Model, Model-NE and MET groups. * p < 0.05, ** p < 0.01 and *** p < 0.001 vs. the sham group, # p < 0.05, ## p < 0.01 and ### p < 0.001 vs. the model group.

    Journal: Journal of Advanced Research

    Article Title: Whole-body mass spectrometry imaging reveals the systemic metabolic disorder and catecholamines biosynthesis alteration on heart-gut axis in heart failure rat

    doi: 10.1016/j.jare.2024.09.001

    Figure Lengend Snippet: Physiological and biochemical analyses of validation experiments. (A) Ejection fraction (EF), fractional shortening (FS), left ventricular internal dimension systole (LVIDs) and left ventricular end-systolic volume (LVESV) were analyzed via ultrasonography in Sham (n = 10), Sham-NE (n = 6), Model (n = 10), Model-NE (n = 9) and MET groups (n = 11). (B) The maximum rate of rising/declining LV intraventricular pressure (±dp/dt max), LV systolic pressure (LVSP) and left ventricular end diastolic pressure (LVEDP) were analyzed via hemodynamic analyses in Sham (n = 10), Sham-NE (n = 6), Model (n = 10), Model-NE (n = 9) and MET groups (n = 11). (C) Serum B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP), lipopolysaccharide (LPS) and diamine oxidase (DAO) were measured by ELISA in Sham (n = 10), Sham-NE (n = 6), Model (n = 10), Model-NE (n = 9) and MET groups (n = 11). (D) Representative images of cardiac tissue sections following H&E or Masson’s trichrome staining. (E) Representative images of colonic tissue sections following H&E staining. (F) Relative abundance of s_Turicibacter_sanguinis in Sham, Sham-NE, Model, Model-NE and MET groups. * p < 0.05, ** p < 0.01 and *** p < 0.001 vs. the sham group, # p < 0.05, ## p < 0.01 and ### p < 0.001 vs. the model group.

    Article Snippet: Following weighing and anesthetization, a Millar catheter (SPR-320NR, Millar,USA) was introduced into the left ventricle, and hemodynamic indices were simultaneously recorded using a physiological signal acquisition system (MP160, BIOPAC System, USA).

    Techniques: Biomarker Discovery, Enzyme-linked Immunosorbent Assay, Staining