TY - JOUR
T1 - Differential effects of azelnidipine and amlodipine on sympathetic nerve activity in patients with primary hypertension
AU - Inomata, Jun Ichiro
AU - Murai, Hisayoshi
AU - Kaneko, Shuichi
AU - Hamaoka, Takuto
AU - Ikeda, Tatsunori
AU - Kobayashi, Daisuke
AU - Usui, Soichiro
AU - Furusho, Hiroshi
AU - Sugiyama, Yu
AU - Takata, Shigeo
AU - Takamura, Masayuki
PY - 2014/9
Y1 - 2014/9
N2 - OBJECTIVE:: Calcium channel blockers (CCBs) are used as antihypertensive agents and have a strong vasodilatory effect; however, the sympathetic activation mediated by baroreflex might cause adverse effects. A recently developed CCB, azelnidipine, decreases the heart rate (HR) while lowering blood pressure (BP), possibly by inhibiting sympathetic nerve activity in animal models. In this study, we evaluated whether azelnidipine inhibited sympathetic nerve activity, compared to amlodipine, in primary hypertensive patients. DESIGN AND METHODS:: We conducted a prospective, randomized, open-label, and crossover study of 14 patients. We measured the patients' BP, HR and baroreflex sensitivity, and directly recorded muscle sympathetic nerve activity (MSNA), via microneurography, after treatment with either CCB for 8 weeks. RESULTS:: Although systolic and diastolic BPs did not differ between the azelnidipine and amlodipine groups, the HR in the azelnidipine group significantly decreased compared with that in the amlodipine group. MSNA was significantly reduced in the azelnidipine compared with the amlodipine group (47.7±14.9 vs. 61.5±10.7bursts per 100 beats, P<0.05). However, no significant difference was observed in terms of the baroreflex control of HR, or MSNA, between the two groups. CONCLUSION:: Our data show, first, that azelnidipine, compared with amlodipine, exerted a favorable effect on sympathetic nerve activity, without affecting baroreflex sensitivity, in hypertensive patients. These results indicate that azelnidipine might be useful for treating hypertensive patients, in whom hypertension is complicated by heart failure and ischemic heart disease.
AB - OBJECTIVE:: Calcium channel blockers (CCBs) are used as antihypertensive agents and have a strong vasodilatory effect; however, the sympathetic activation mediated by baroreflex might cause adverse effects. A recently developed CCB, azelnidipine, decreases the heart rate (HR) while lowering blood pressure (BP), possibly by inhibiting sympathetic nerve activity in animal models. In this study, we evaluated whether azelnidipine inhibited sympathetic nerve activity, compared to amlodipine, in primary hypertensive patients. DESIGN AND METHODS:: We conducted a prospective, randomized, open-label, and crossover study of 14 patients. We measured the patients' BP, HR and baroreflex sensitivity, and directly recorded muscle sympathetic nerve activity (MSNA), via microneurography, after treatment with either CCB for 8 weeks. RESULTS:: Although systolic and diastolic BPs did not differ between the azelnidipine and amlodipine groups, the HR in the azelnidipine group significantly decreased compared with that in the amlodipine group. MSNA was significantly reduced in the azelnidipine compared with the amlodipine group (47.7±14.9 vs. 61.5±10.7bursts per 100 beats, P<0.05). However, no significant difference was observed in terms of the baroreflex control of HR, or MSNA, between the two groups. CONCLUSION:: Our data show, first, that azelnidipine, compared with amlodipine, exerted a favorable effect on sympathetic nerve activity, without affecting baroreflex sensitivity, in hypertensive patients. These results indicate that azelnidipine might be useful for treating hypertensive patients, in whom hypertension is complicated by heart failure and ischemic heart disease.
UR - https://www.scopus.com/pages/publications/84906092308
UR - https://www.scopus.com/pages/publications/84906092308#tab=citedBy
U2 - 10.1097/HJH.0000000000000270
DO - 10.1097/HJH.0000000000000270
M3 - Article
C2 - 24979307
AN - SCOPUS:84906092308
SN - 0263-6352
VL - 32
SP - 1898
EP - 1904
JO - Journal of hypertension
JF - Journal of hypertension
IS - 9
ER -