K. Sakata et al., Effects of amlodipine and cilnidipine on cardiac sympathetic nervous system and neurohormonal status in essential hypertension, HYPERTENSIO, 33(6), 1999, pp. 1447-1452
Citations number
46
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
N-Type calcium channel antagonists may suppress sympathetic activity, The p
urpose of this study was to assess the effects of amlodipine and cilnidipin
e on the cardiac sympathetic nervous system and the neurohormonal status of
essential hypertension. I-123-metaiodobenzylguanidine (MIBG) cardiac imagi
ng was performed and blood samples were taken to determine plasma renin act
ivity and plasma norepinephrine concentration before and 3 months after dru
g administration in 47 patients with mild essential hypertension. Twenty-fo
ur of the patients were treated with 5 to 10 mg/d of amlodipine; the other
23 were treated with 10 to 20 mg/d of cilnidipine. For comparison, 12 normo
tensive subjects were also studied. No significant differences were found i
n the basal characteristics between the 2 hypertensive groups. In both hype
rtensive groups, both the systolic and diastolic blood pressures were signi
ficantly reduced to similar levels 3 months after drug treatment. Before th
e drug treatment, the 2 hypertensive groups had a significantly higher wash
out rate and lower heart-to-mediastinum (H/M) ratio compared with the normo
tensive subjects. The H/M ratio significantly increased (P<0.05) in combina
tion with a decreased washout rate (P<0.02) after drug treatment in the cil
nidipine group. In the amlodipine group, a significant decrease in washout
rate (P<0.04) was noted, without an increase in the H/M ratio. However, no
significant changes were found in plasma renin activity and plasma norepine
phrine concentration in either group. Thus, in patients with essential hype
rtension, cilnidipine suppressed cardiac sympathetic overactivity and amlod
ipine had a little suppressive effect. Cilnidipine may provide a new strate
gy for treatment of cardiovascular diseases with sympathetic overactivity.