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Kent Scientific Corp coda noninvasive blood pressure system
Coda Noninvasive Blood Pressure System, supplied by Kent Scientific Corp, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/coda+noninvasive+system/coda+system/pm42045383-73-30-35
Average 86 stars, based on 1 article reviews
coda noninvasive blood pressure system - by Bioz Stars, 2026-09
86/100 stars

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Article Title: Vericiguat improves cardiac remodelling and function in rats with doxorubicin‐induced cardiomyopathy
Article Snippet: Blood pressure was assessed using the CODA noninvasive BP system (Kent Scientific) via tail‐cuff methodology.

Article Title: xCT/Slc7a11 promotes pulmonary arterial hypertension by disrupting AMPKα suppression of mTOR activation.
Article Snippet: While mTOR plays a key role in the development of pulmonary arterial hypertension (PAH), its suppressor, AMPKα, acts as an inhibitor.. Although mTOR-driven transcriptional upregulation of the plasma membrane exchanger and amino acid transporter xCT, encoded by the Slc7a11 gene, is critical for cell proliferation and tumorigenesis, the involvement of xCT in PAH remains unexplored.. In this study, we found that xCT expression was elevated in hypoxia-treated human pulmonary arterial endothelial cells (HPAECs) and the lungs of hypoxiaexposed mice and Sugen5416/hypoxia (SuHx)-induced PAH mice.

Article Title: Dietary fiber intake impacts gut bacterial and viral populations in a hypertensive mouse model.
Article Snippet: Systolic BP was measured using tail-cuff in a CODA noninvasive BP system (Kent Scientific Corporation).

Article Title: Vericiguat improves cardiac remodelling and function in rats with doxorubicin-induced cardiomyopathy.
Article Snippet: Blood pressure and fasting blood glucose measurement Blood pressure was assessed using the CODA noninvasive BP system (Kent Scientific) via tail-cuff methodology.

Article Title: Genetic mapping of electrocardiographic parameters in BXD strains reveals Chromosome 3 loci to be associated with cardiac repolarization abnormalities.
Article Snippet: 149 150 Blood pressure and echocardiography parameters 151 The CODA noninvasive BP system (a tail-cuff method, Kent Scientific Corporation) measured systolic 152 and diastolic blood pressure by determining the tail blood volume.

Article Title: Endothelial cell (EC)-specific CTGF/CCN2 Expression Increases EC Reprogramming and Atherosclerosis.
Article Snippet: Arterial endothelial cells (ECs) reside in a complex biomechanical environment.. ECs sense and respond to wall shear stress.. Low and oscillatory wall shear stress is characteristic of disturbed flow and commonly found at arterial bifurcations and around atherosclerotic 4 plaques.

Article Title: Dietary fiber intake impacts gut bacterial and viral populations in a hypertensive mouse model
Article Snippet: Systolic BP was measured using tail-cuff in a CODA noninvasive BP system (Kent Scientific Corporation).

Article Title: Longitudinal Changes in Blood Pressure are Preceded by Changes in Albuminuria and Accelerated by Increasing Dietary Sodium Intake
Article Snippet: Systolic (SBP) and diastolic BP (DBP), as well as heart rate (HR) were measured in conscious animals every month, for 13 months, using tail-cuff plethysmography and the CODA noninvasive BP system (KENT Scientific Corporation, Torrington, CT), as previously described by us 18 , 19 .



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Kent Scientific Corp noninvasive computerized coda tail cuff blood pressure system
a Experiment design. 16-week-old C57BL/6 J mice were infused with AngII (1000 ng/kg·min − 1 ) for 28 days. After 7 days of infusion, the mice were daily injected with vehicle, dihydropyridine CCBs [amlodipine (1 mg/kg/day) or nifedipine (20 mg/kg/day)], benzothiazepine CCB [diltiazem (8 mg/kg/day)], phenylalkylamine CCBs [verapamil (12 mg/kg/day)]. b SBP was measured <t>by</t> <t>tail-cuff</t> at −7, 0, 3, 7, 14, 21 days after vehicle/CCBs treatment. c –e Ultrasound-monitored maximal inner diameters of the aortic root, ascending aorta, and aortic arch at 0, 7, 14, 21 days. f Representative ultrasound images of thoracic aorta after 21 days of vehicle/CCB treatment. g –i Monitoring of rd-PWV and ascending aortic strain in mice at different time points by M-mode ultrasound. ( g ) Schematic illustration of calculation method. ( h ) rd-PWV. i Ascending aortic strain. j Representative ex vivo morphology of thoracic aortas. Scale bar=2 mm. k –m Maximal external diameters of ascending aorta ( k ), aortic arch ( l ), and descending aorta ( m ). Data presentation : Data in ( b –e, h , i, k-m ) are presented as mean ± SEM. For some points, SEM is smaller than the symbol size and not visually discernible. Each data point represents an individual mouse as a biological replicate with similar results. The initial sample sizes per group were: Saline + Vehicle ( n = 7), AngII + Vehicle ( n = 13), AngII + Amlodipine ( n = 12), AngII + Nifedipine ( n = 12), AngII + Diltiazem ( n = 11), AngII + Verapamil ( n = 11). Due to mortality during the experimental period, exact n at each time point is provided in the Source Data file. Statistical analysis : Two-sided one-way ANOVA with Dunnett multiple comparisons test, Brown-Forsythe and Welch ANOVA with Dunnett T3 multiple comparisons test or Kruskal-Wallis test with Dunn’s multiple comparisons was used as appropriate for ( b-e , h , i ) at different time points (detailed for each comparison in the Source Data file). * P < 0.05 vs. AngII + Vehicle group. Exact P -values for all comparisons are provided in the Source Data file. Statistical analysis of ( k –m ) were performed using two-sided Brown-Forsythe and Welch ANOVA with Dunnett T3 multiple comparisons test. Source data are provided as a Source Data file. AngII angiotensin II, SBP systolic blood pressure, CCB calcium channel blocker, rd-PWV root to descending aorta pulse wave velocity.
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a Experiment design. 16-week-old C57BL/6 J mice were infused with AngII (1000 ng/kg·min − 1 ) for 28 days. After 7 days of infusion, the mice were daily injected with vehicle, dihydropyridine CCBs [amlodipine (1 mg/kg/day) or nifedipine (20 mg/kg/day)], benzothiazepine CCB [diltiazem (8 mg/kg/day)], phenylalkylamine CCBs [verapamil (12 mg/kg/day)]. b SBP was measured by tail-cuff at −7, 0, 3, 7, 14, 21 days after vehicle/CCBs treatment. c –e Ultrasound-monitored maximal inner diameters of the aortic root, ascending aorta, and aortic arch at 0, 7, 14, 21 days. f Representative ultrasound images of thoracic aorta after 21 days of vehicle/CCB treatment. g –i Monitoring of rd-PWV and ascending aortic strain in mice at different time points by M-mode ultrasound. ( g ) Schematic illustration of calculation method. ( h ) rd-PWV. i Ascending aortic strain. j Representative ex vivo morphology of thoracic aortas. Scale bar=2 mm. k –m Maximal external diameters of ascending aorta ( k ), aortic arch ( l ), and descending aorta ( m ). Data presentation : Data in ( b –e, h , i, k-m ) are presented as mean ± SEM. For some points, SEM is smaller than the symbol size and not visually discernible. Each data point represents an individual mouse as a biological replicate with similar results. The initial sample sizes per group were: Saline + Vehicle ( n = 7), AngII + Vehicle ( n = 13), AngII + Amlodipine ( n = 12), AngII + Nifedipine ( n = 12), AngII + Diltiazem ( n = 11), AngII + Verapamil ( n = 11). Due to mortality during the experimental period, exact n at each time point is provided in the Source Data file. Statistical analysis : Two-sided one-way ANOVA with Dunnett multiple comparisons test, Brown-Forsythe and Welch ANOVA with Dunnett T3 multiple comparisons test or Kruskal-Wallis test with Dunn’s multiple comparisons was used as appropriate for ( b-e , h , i ) at different time points (detailed for each comparison in the Source Data file). * P < 0.05 vs. AngII + Vehicle group. Exact P -values for all comparisons are provided in the Source Data file. Statistical analysis of ( k –m ) were performed using two-sided Brown-Forsythe and Welch ANOVA with Dunnett T3 multiple comparisons test. Source data are provided as a Source Data file. AngII angiotensin II, SBP systolic blood pressure, CCB calcium channel blocker, rd-PWV root to descending aorta pulse wave velocity.

Journal: Nature Communications

Article Title: Calcium channel blockers increase the risk of aortic aneurysm and dissection

doi: 10.1038/s41467-025-68086-5

Figure Lengend Snippet: a Experiment design. 16-week-old C57BL/6 J mice were infused with AngII (1000 ng/kg·min − 1 ) for 28 days. After 7 days of infusion, the mice were daily injected with vehicle, dihydropyridine CCBs [amlodipine (1 mg/kg/day) or nifedipine (20 mg/kg/day)], benzothiazepine CCB [diltiazem (8 mg/kg/day)], phenylalkylamine CCBs [verapamil (12 mg/kg/day)]. b SBP was measured by tail-cuff at −7, 0, 3, 7, 14, 21 days after vehicle/CCBs treatment. c –e Ultrasound-monitored maximal inner diameters of the aortic root, ascending aorta, and aortic arch at 0, 7, 14, 21 days. f Representative ultrasound images of thoracic aorta after 21 days of vehicle/CCB treatment. g –i Monitoring of rd-PWV and ascending aortic strain in mice at different time points by M-mode ultrasound. ( g ) Schematic illustration of calculation method. ( h ) rd-PWV. i Ascending aortic strain. j Representative ex vivo morphology of thoracic aortas. Scale bar=2 mm. k –m Maximal external diameters of ascending aorta ( k ), aortic arch ( l ), and descending aorta ( m ). Data presentation : Data in ( b –e, h , i, k-m ) are presented as mean ± SEM. For some points, SEM is smaller than the symbol size and not visually discernible. Each data point represents an individual mouse as a biological replicate with similar results. The initial sample sizes per group were: Saline + Vehicle ( n = 7), AngII + Vehicle ( n = 13), AngII + Amlodipine ( n = 12), AngII + Nifedipine ( n = 12), AngII + Diltiazem ( n = 11), AngII + Verapamil ( n = 11). Due to mortality during the experimental period, exact n at each time point is provided in the Source Data file. Statistical analysis : Two-sided one-way ANOVA with Dunnett multiple comparisons test, Brown-Forsythe and Welch ANOVA with Dunnett T3 multiple comparisons test or Kruskal-Wallis test with Dunn’s multiple comparisons was used as appropriate for ( b-e , h , i ) at different time points (detailed for each comparison in the Source Data file). * P < 0.05 vs. AngII + Vehicle group. Exact P -values for all comparisons are provided in the Source Data file. Statistical analysis of ( k –m ) were performed using two-sided Brown-Forsythe and Welch ANOVA with Dunnett T3 multiple comparisons test. Source data are provided as a Source Data file. AngII angiotensin II, SBP systolic blood pressure, CCB calcium channel blocker, rd-PWV root to descending aorta pulse wave velocity.

Article Snippet: Briefly, a noninvasive computerized CODA tail-cuff blood pressure system (Kent Scientific, Torrington, CT, USA) was used to measure mouse SBP.

Techniques: Injection, Ex Vivo, Saline, Comparison

a Experiment design. 8-week-old mice infrarenal abdominal aortas were incubated with PBS or elastase (10 mg/ml) and then daily injected with vehicle, amlodipine (1 mg/kg/day), nifedipine (20 mg/kg/day), diltiazem (8 mg/kg/day) or verapamil (12 mg/kg/day) for 14 days. b SBP was measured by tail-cuff at 14 days after vehicle/CCBs treatment. c Representative ex vivo morphology of aortas. Scale bar=2 mm. d Maximal external diameter of abdominal aorta. e , f Representative image of abdominal aorta elastin Van Gieson staining ( e ) and statistical analysis on elastin degradation grade. Scale bar=250/50 μm. Data presentation: Data in ( b , d , e , f ) are presented as mean ± SEM. Each data point represents an individual mouse as a biological replicate with similar results. The sample sizes per group were: PBS + vehicle ( n = 3), Elastase + vehicle ( n = 9), Elastase + amlodipine ( n = 11), Elastase + nifedipine ( n = 10), Elastase + diltiazem ( n = 12), Elastase + verapamil ( n = 9). Statistical analysis: Statistical analysis of ( b ) were performed using two-sided one-way ANOVA with Dunnett multiple comparisons test. Statistical analysis of ( d ) were performed using two-sided Brown-Forsythe and Welch ANOVA with Dunnett T3 multiple comparisons test. Statistical analysis of ( f ) were performed using two-sided Kruskal-Wallis test with Dunn’s multiple comparisons. Source data are provided as a Source Data file. CCB calcium channel blocker, PBS phosphate buffered saline, SBP systolic blood pressure.

Journal: Nature Communications

Article Title: Calcium channel blockers increase the risk of aortic aneurysm and dissection

doi: 10.1038/s41467-025-68086-5

Figure Lengend Snippet: a Experiment design. 8-week-old mice infrarenal abdominal aortas were incubated with PBS or elastase (10 mg/ml) and then daily injected with vehicle, amlodipine (1 mg/kg/day), nifedipine (20 mg/kg/day), diltiazem (8 mg/kg/day) or verapamil (12 mg/kg/day) for 14 days. b SBP was measured by tail-cuff at 14 days after vehicle/CCBs treatment. c Representative ex vivo morphology of aortas. Scale bar=2 mm. d Maximal external diameter of abdominal aorta. e , f Representative image of abdominal aorta elastin Van Gieson staining ( e ) and statistical analysis on elastin degradation grade. Scale bar=250/50 μm. Data presentation: Data in ( b , d , e , f ) are presented as mean ± SEM. Each data point represents an individual mouse as a biological replicate with similar results. The sample sizes per group were: PBS + vehicle ( n = 3), Elastase + vehicle ( n = 9), Elastase + amlodipine ( n = 11), Elastase + nifedipine ( n = 10), Elastase + diltiazem ( n = 12), Elastase + verapamil ( n = 9). Statistical analysis: Statistical analysis of ( b ) were performed using two-sided one-way ANOVA with Dunnett multiple comparisons test. Statistical analysis of ( d ) were performed using two-sided Brown-Forsythe and Welch ANOVA with Dunnett T3 multiple comparisons test. Statistical analysis of ( f ) were performed using two-sided Kruskal-Wallis test with Dunn’s multiple comparisons. Source data are provided as a Source Data file. CCB calcium channel blocker, PBS phosphate buffered saline, SBP systolic blood pressure.

Article Snippet: Briefly, a noninvasive computerized CODA tail-cuff blood pressure system (Kent Scientific, Torrington, CT, USA) was used to measure mouse SBP.

Techniques: Incubation, Injection, Ex Vivo, Staining, Saline