» Articles » PMID: 6184568

Contrasting Effects of Nifedipine, Captopril, and Propranolol in Normotensive and Hypertensive Subjects

Overview
Date 1982 Jan 1
PMID 6184568
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Nifedipine was given to 15 patients with essential hypertension for 6 weeks and to 8 normotensive subjects for 5 days. In the hypertensives, 30 min after the first dose of nifedipine (5-mg capsule), there was a 13.9% fall in mean blood pressure (p less than 0.001), and, at the 6th week of treatment at the maximum dose of 20 mg t.d.s., a 20.6% fall in mean blood pressure (p less than 0.001). In the normotensive subjects, 30 min after the first dose of 5 mg of nifedipine, there was a 2.3% fall in mean blood pressure (NS), and on the 5th day with the maximum dose of 20 mg t.d.s., the fall was 2.2% (NS). In view of the difference in age between these normotensive and hypertensive subjects, a larger group of patients with essential hypertension and older normotensive subjects were also studied acutely after a single 5-mg capsule of nifedipine. Thirty minutes after the first dose of nifedipine in the larger group of hypertensives, there was a significant fall in mean blood pressure (10.4%; p less than 0.001, n = 33). In the normotensive subjects, there was also a significant fall in mean blood pressure (4.7%; p less than 0.01, n = 29). This was significantly less than in the hypertensives (p less than 0.001). In both the normotensive and hypertensive subjects, there was a significant correlation between pretreatment blood pressure and percentage decrease in blood pressure with nifedipine. Nifedipine, therefore, has a greater blood pressure-lowering effect the higher the initial blood pressure. This finding is compatible with the idea that nifedipine reveals a functional abnormality of vascular smooth muscle that becomes greater the higher the blood pressure.

Citing Articles

The beneficial effects of omega-3 polyunsaturated fatty acids on controlling blood pressure: An umbrella meta-analysis.

Musazadeh V, Kavyani Z, Naghshbandi B, Dehghan P, Vajdi M Front Nutr. 2022; 9:985451.

PMID: 36061895 PMC: 9435313. DOI: 10.3389/fnut.2022.985451.


Fenoldopam Sensitizes Primary Cilia-Mediated Mechanosensing to Promote Osteogenic Intercellular Signaling and Whole Bone Adaptation.

Spasic M, Duffy M, Jacobs C J Bone Miner Res. 2022; 37(5):972-982.

PMID: 35230705 PMC: 9098671. DOI: 10.1002/jbmr.4536.


The β3 subunit contributes to vascular calcium channel upregulation and hypertension in angiotensin II-infused C57BL/6 mice.

Kharade S, Sonkusare S, Srivastava A, Thakali K, Fletcher T, Rhee S Hypertension. 2012; 61(1):137-42.

PMID: 23129698 PMC: 3748590. DOI: 10.1161/HYPERTENSIONAHA.112.197863.


A mathematical model for dynamics of cardiovascular drug action: application to intravenous dihydropyridines in healthy volunteers.

Francheteau P, Steimer J, Merdjan H, GUERRET M, Dubray C J Pharmacokinet Biopharm. 1993; 21(5):489-514.

PMID: 8145128 DOI: 10.1007/BF01059111.


The effect of felodipine on forearm haemodynamics and the myogenic response of the forearm resistance vessels in normal man.

Mace P, Stallard T, Littler W Br J Clin Pharmacol. 1985; 20(4):383-6.

PMID: 4074606 PMC: 1400883. DOI: 10.1111/j.1365-2125.1985.tb05081.x.