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Central integration and neural control of blood pressure during the cold pressor test: a comparison between hydrochlorothiazide and aliskiren

Individuals with hypertension and sympathetic overactivity are at risk for cardiovascular events. Renin inhibitors are new while thiazide diuretics are first-class drugs used for treatment of hypertension. The purpose of this study was to determine whether 6 months of treatment with aliskiren (ALSK)...

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Autores principales: Jarvis, Sara S, Okada, Yoshiyuki, Levine, Benjamin D, Fu, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600375/
https://www.ncbi.nlm.nih.gov/pubmed/26465969
http://dx.doi.org/10.14814/phy2.12502
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author Jarvis, Sara S
Okada, Yoshiyuki
Levine, Benjamin D
Fu, Qi
author_facet Jarvis, Sara S
Okada, Yoshiyuki
Levine, Benjamin D
Fu, Qi
author_sort Jarvis, Sara S
collection PubMed
description Individuals with hypertension and sympathetic overactivity are at risk for cardiovascular events. Renin inhibitors are new while thiazide diuretics are first-class drugs used for treatment of hypertension. The purpose of this study was to determine whether 6 months of treatment with aliskiren (ALSK) or hydrochlorothiazide (HCTZ) would alter blood pressure (BP) and muscle sympathetic nerve activity (MSNA) indices in older mild hypertensives during a cold pressor test (CPT). We hypothesized that the ALSK group would demonstrate a blunted response compared to HCTZ. Nineteen (9 men, 10 women) subjects performed a CPT pre- and post treatment where heart rate (HR), systolic BP (SBP) and diastolic BP (DBP), and MSNA were measured. Blood samples were withdrawn for assessment of renal-adrenal hormones. Both medications lowered ambulatory SBP and DBP (P < 0.05). Direct renin tended to be higher in the ALSK group after treatment (P = 0.081). Aldosterone was higher in the HCTZ group after treatment (P < 0.001). As expected, both groups showed increases in HR, SBP, DBP, and MSNA during the CPT (all P < 0.05). All cardiovascular and MSNA responses were similar pre- and post treatment in both groups (peak CPT SBP: 26 ± 10 vs. 17 ± 21 and 21 ± 20 vs. 29 ± 15 mmHg for pre vs. post for HCTZ and ALSK, respectively; peak CPT MSNA burst frequency: 13 ± 8 vs. 11 ± 11 and 11 ± 17 vs. 6 ± 13 bursts/min; all P > 0.05). Treatment with these antihypertensive medications lowered BP but was not successful in lowering the responsiveness to the CPT.
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spelling pubmed-46003752015-10-15 Central integration and neural control of blood pressure during the cold pressor test: a comparison between hydrochlorothiazide and aliskiren Jarvis, Sara S Okada, Yoshiyuki Levine, Benjamin D Fu, Qi Physiol Rep Original Research Individuals with hypertension and sympathetic overactivity are at risk for cardiovascular events. Renin inhibitors are new while thiazide diuretics are first-class drugs used for treatment of hypertension. The purpose of this study was to determine whether 6 months of treatment with aliskiren (ALSK) or hydrochlorothiazide (HCTZ) would alter blood pressure (BP) and muscle sympathetic nerve activity (MSNA) indices in older mild hypertensives during a cold pressor test (CPT). We hypothesized that the ALSK group would demonstrate a blunted response compared to HCTZ. Nineteen (9 men, 10 women) subjects performed a CPT pre- and post treatment where heart rate (HR), systolic BP (SBP) and diastolic BP (DBP), and MSNA were measured. Blood samples were withdrawn for assessment of renal-adrenal hormones. Both medications lowered ambulatory SBP and DBP (P < 0.05). Direct renin tended to be higher in the ALSK group after treatment (P = 0.081). Aldosterone was higher in the HCTZ group after treatment (P < 0.001). As expected, both groups showed increases in HR, SBP, DBP, and MSNA during the CPT (all P < 0.05). All cardiovascular and MSNA responses were similar pre- and post treatment in both groups (peak CPT SBP: 26 ± 10 vs. 17 ± 21 and 21 ± 20 vs. 29 ± 15 mmHg for pre vs. post for HCTZ and ALSK, respectively; peak CPT MSNA burst frequency: 13 ± 8 vs. 11 ± 11 and 11 ± 17 vs. 6 ± 13 bursts/min; all P > 0.05). Treatment with these antihypertensive medications lowered BP but was not successful in lowering the responsiveness to the CPT. John Wiley & Sons, Ltd 2015-09-14 /pmc/articles/PMC4600375/ /pubmed/26465969 http://dx.doi.org/10.14814/phy2.12502 Text en © 2015 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Jarvis, Sara S
Okada, Yoshiyuki
Levine, Benjamin D
Fu, Qi
Central integration and neural control of blood pressure during the cold pressor test: a comparison between hydrochlorothiazide and aliskiren
title Central integration and neural control of blood pressure during the cold pressor test: a comparison between hydrochlorothiazide and aliskiren
title_full Central integration and neural control of blood pressure during the cold pressor test: a comparison between hydrochlorothiazide and aliskiren
title_fullStr Central integration and neural control of blood pressure during the cold pressor test: a comparison between hydrochlorothiazide and aliskiren
title_full_unstemmed Central integration and neural control of blood pressure during the cold pressor test: a comparison between hydrochlorothiazide and aliskiren
title_short Central integration and neural control of blood pressure during the cold pressor test: a comparison between hydrochlorothiazide and aliskiren
title_sort central integration and neural control of blood pressure during the cold pressor test: a comparison between hydrochlorothiazide and aliskiren
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600375/
https://www.ncbi.nlm.nih.gov/pubmed/26465969
http://dx.doi.org/10.14814/phy2.12502
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