Antihypertensive and humoral effects of verapamil and nifedipine in essential hypertension
- PMID: 6184562
Antihypertensive and humoral effects of verapamil and nifedipine in essential hypertension
Abstract
The aim of this study was to investigate and compare the effects of two calcium antagonist drugs, verapamil (VER) and nifedipine (NIF), on blood pressure (BP), heart rate (HR), plasma catecholamines (pCA), renin (PRA), plasma aldosterone (pALD), and plasma volume (PV) in a group of patients with mild to moderate essential hypertension. In 12 hypertensive patients on a fixed normal sodium and potassium intake, VER (80 mg t.i.d., per os) first and then NIF (10 mg, t.i.d. per os), or vice versa according to a random sequence, were each given for 8 days, with an interval of 5 days between the two treatments. Both NIF and VER significantly reduced BP (p less than 0.001); this reduction was quantitatively similar in both treatment schedules. Supine and standing PRA, pALD, and PV were not significantly affected by VER or NIF. HR and pCA were unchanged after VER, whereas they were significantly increased (p less than 0.05, at least) mainly in standing position after NIF treatment. The antihypertensive and metabolic effects of VER (80 mg t.i.d.) and NIF (10 mg t.i.d.) were maintained after chronic treatment (4 months with VER in 10 patients and 2 months with NIF in 12 patients). After 2 months of treatment with VER (160 mg t.i.d.) in 18 patients, BP was further reduced, while pCA were slightly increased. In conclusion, VER and NIF are effective and equipotent antihypertensive agents that do not induce significant renin stimulation or fluid retention; adrenergic stimulation seems to be greater with NIF, which should be taken into account in the clinical use of these drugs.
Similar articles
-
[Relationship of the renin-angiotensin-aldosterone system with auricular natriuretic factor in its response to the action of thiazide diuretics and to nifedipine, a sustained-release calcium antagonist].Med Clin (Barc). 1994 Jan 22;102(2):41-5. Med Clin (Barc). 1994. PMID: 8133694 Spanish.
-
Comparison of cardiovascular, renal, and humoral effects of acute administration of two calcium channel blockers in normotensive and hypertensive subjects.J Cardiovasc Pharmacol. 1982;4 Suppl 3:S319-24. J Cardiovasc Pharmacol. 1982. PMID: 6184561
-
Calcium antagonists in the treatment of hypertension: a critical overview.Adv Nephrol Necker Hosp. 1985;14:197-232. Adv Nephrol Necker Hosp. 1985. PMID: 3919532 Review. No abstract available.
-
Humoral and haemodynamic interactions between clonidine and nifedipine in human essential hypertension.J Hypertens Suppl. 1985 Dec;3(3):S227-9. J Hypertens Suppl. 1985. PMID: 2856710 Clinical Trial.
-
Calcium-channel blocking agents.Clin Pharm. 1982 Jan-Feb;1(1):17-33. Clin Pharm. 1982. PMID: 6764159 Review.
Cited by
-
Effect of verapamil on renal plasma flow, glomerular filtration rate and plasma angiotensin II, aldosterone and arginine vasopressin in essential hypertension.Eur J Clin Pharmacol. 1985;29(3):257-61. doi: 10.1007/BF00544077. Eur J Clin Pharmacol. 1985. PMID: 4076325 Clinical Trial.
-
Renal effects of antihypertensive drugs.Drugs. 1989 Jun;37(6):900-25. doi: 10.2165/00003495-198937060-00005. Drugs. 1989. PMID: 2667938 Review.
-
Calcium channel antagonists, Part I: Fundamental properties: mechanisms, classification, sites of action.Cardiovasc Drugs Ther. 1987 Dec;1(4):411-30. doi: 10.1007/BF02209083. Cardiovasc Drugs Ther. 1987. PMID: 2856470 Review.
-
Long-term therapy with slow-release nifedipine in essential hypertension.Cardiovasc Drugs Ther. 1990 Aug;4 Suppl 5:941-5. doi: 10.1007/BF02018297. Cardiovasc Drugs Ther. 1990. PMID: 2076404 Clinical Trial.
-
The effect of 8 weeks treatment with the calcium antagonist felodipine on blood pressure, heart rate, working capacity, plasma renin activity, plasma angiotensin II, urinary catecholamines and aldosterone in patients with essential hypertension.Br J Clin Pharmacol. 1986 Jun;21(6):633-40. doi: 10.1111/j.1365-2125.1986.tb05227.x. Br J Clin Pharmacol. 1986. PMID: 3527242 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical
Research Materials