Your browser doesn't support javascript.
loading
The angiotensin II type 1 receptor blocker azilsartan can overwhelm the sympathetic nerve activation stimulated by coadministration of calcium channel blockers.
Fukuda, Michio; Isobe-Sasaki, Yukako; Sato, Ryo; Miura, Toshiyuki; Mizuno, Masashi; Ono, Minamo; Kiyono, Ken; Yamamoto, Yoshiharu; Hayano, Junichiro; Ohte, Nobuyuki.
Affiliation
  • Fukuda M; 1 Department of Cardio-Renal Medicine and Hypertension, Nagoya City University Graduate School of Medical Sciences, Japan.
  • Isobe-Sasaki Y; 1 Department of Cardio-Renal Medicine and Hypertension, Nagoya City University Graduate School of Medical Sciences, Japan.
  • Sato R; 1 Department of Cardio-Renal Medicine and Hypertension, Nagoya City University Graduate School of Medical Sciences, Japan.
  • Miura T; 1 Department of Cardio-Renal Medicine and Hypertension, Nagoya City University Graduate School of Medical Sciences, Japan.
  • Mizuno M; 1 Department of Cardio-Renal Medicine and Hypertension, Nagoya City University Graduate School of Medical Sciences, Japan.
  • Ono M; 1 Department of Cardio-Renal Medicine and Hypertension, Nagoya City University Graduate School of Medical Sciences, Japan.
  • Kiyono K; 2 Department of Mechanical Science and Bioengineering, Osaka University, Japan.
  • Yamamoto Y; 3 Department of Physical and Health Education, University of Tokyo Graduate School of Education, Japan.
  • Hayano J; 4 Department of Medical Education, Nagoya City University Graduate School of Medical Sciences, Japan.
  • Ohte N; 1 Department of Cardio-Renal Medicine and Hypertension, Nagoya City University Graduate School of Medical Sciences, Japan.
J Renin Angiotensin Aldosterone Syst ; 20(1): 1470320319839525, 2019.
Article in En | MEDLINE | ID: mdl-30915878
OBJECTIVE:: In our recent study, non-Gaussianity of heart rate variability (λ25s), an indicator of sympathetic nerve activity, did not change during two-day treatment with the angiotensin II type 1 receptor blocker (ARB) azilsartan. Coadministration of calcium channel blockers (CCBs) might affect the study results. METHODS:: In this subanalysis, 20 patients with chronic kidney disease (14 men; age 61±15 years) were divided into three groups: patients with coadministration of L-type CCB, patients without coadministration of CCB, and patients with coadministration of sympathoinhibitory (L/T- or L/T/N-type) CCB. λ25s was calculated separately in daytime and nighttime. RESULTS:: Daytime λ25s at baseline was higher in patients with L-type CCB coadministration (0.62±0.18, n = 5) compared with those without CCB (0.49±0.13, n = 11) and those with sympathoinhibitory CCB (0.46±0.06, n = 4). The relationship between the changes in daytime λ25s and systolic blood pressure was positive in patients with L-type CCB coadministration, whereas the relationship was inverse in the other two groups. A larger decrease in daytime λ25s was shown in patients with L-type CCB coadministration compared with those in the other two groups. CONCLUSIONS:: CCBs, as well as diuretics, are recommended as second-line antihypertensive agents. Our results suggested that ARBs can overwhelm the activation of sympathetic nerve activity stimulated by coadministration of L-type CCBs.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxadiazoles / Sympathetic Nervous System / Benzimidazoles / Calcium Channel Blockers / Angiotensin II Type 1 Receptor Blockers Limits: Female / Humans / Male / Middle aged Language: En Journal: J Renin Angiotensin Aldosterone Syst Journal subject: FISIOLOGIA Year: 2019 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxadiazoles / Sympathetic Nervous System / Benzimidazoles / Calcium Channel Blockers / Angiotensin II Type 1 Receptor Blockers Limits: Female / Humans / Male / Middle aged Language: En Journal: J Renin Angiotensin Aldosterone Syst Journal subject: FISIOLOGIA Year: 2019 Document type: Article Affiliation country: Country of publication: