Literature DB >> 7512486

Effect of verapamil on atherosclerosis.

G Leonetti1, L Sampieri, R Bragato, G Comerio.   

Abstract

Whether antihypertensive agents exert an antiatherosclerotic effect by blood pressure reduction or independently of their antihypertensive effect is clinically relevant. Animal studies have generally shown that the calcium antagonist verapamil has a preventive rather than a therapeutic antiatherosclerotic effect, which is independent of its antihypertensive effect. However, doses used in animal studies were much higher than those administered to humans and, in animals, the time of administration of verapamil coincided with the application of atherogenic stimulus. Human studies have given controversial results. Verapamil appears to effectively reduce the restenosis rate after coronary angioplasty. However, in patients with coronary stenosis who were undergoing bypass surgery, results were conflicting: a retrospective study provided positive results, while a prospective study gave negative results. An ongoing study investigating the effect of verapamil on the carotid arteries of hypertensive patients could help clarify the relationship between blood pressure reduction and the progression, regression or development of carotid lesions.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 7512486     DOI: 10.2165/00003495-199300462-00014

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  24 in total

Review 1.  Antiperoxidative actions of calcium antagonists and atherogenesis.

Authors:  P D Henry
Journal:  J Cardiovasc Pharmacol       Date:  1991       Impact factor: 3.105

2.  Vascular protection of lacidipine in salt-loaded Dahl-S rats at nonsustained antihypertensive doses.

Authors:  P Cristofori; A Terron; D Micheli; G Bertolini; G Gaviraghi; C Carpi
Journal:  J Cardiovasc Pharmacol       Date:  1991       Impact factor: 3.105

Review 3.  The antiatherogenic potential of calcium antagonists.

Authors:  D B Weinstein
Journal:  J Cardiovasc Pharmacol       Date:  1988       Impact factor: 3.105

4.  Failure of diltiazem to prevent restenosis after percutaneous transluminal coronary angioplasty.

Authors:  T Corcos; P R David; P G Val; J Renkin; V Dangoisse; H G Rapold; M G Bourassa
Journal:  Am Heart J       Date:  1985-05       Impact factor: 4.749

5.  Interventional clinical trials using noninvasive ultrasound end points: the Multicenter Isradipine/Diuretic Atherosclerosis Study. The MIDAS Research Group.

Authors:  M G Bond; H L Strickland; S K Wilmoth; A Safrit; R Phillips; L Szostak
Journal:  J Cardiovasc Pharmacol       Date:  1990       Impact factor: 3.105

6.  Atherosclerosis and calcium antagonists: the VHAS. The Verapamil-Hypertension Atherosclerosis Study (VHAS) Investigators.

Authors:  A Zanchetti; B Magnani; C Dal Palù
Journal:  J Hum Hypertens       Date:  1992-12       Impact factor: 3.012

7.  Antiatherogenic activity of FR34235 (Nilvadipine), a new potent calcium antagonist. Effect on cuff-induced intimal thickening of rabbit carotid artery.

Authors:  A Nomoto; J Hirosumi; C Sekiguchi; S Mutoh; I Yamaguchi; H Aoki
Journal:  Atherosclerosis       Date:  1987-04       Impact factor: 5.162

8.  Retardation of angiographic progression of coronary artery disease by nifedipine. Results of the International Nifedipine Trial on Antiatherosclerotic Therapy (INTACT). INTACT Group Investigators.

Authors:  P R Lichtlen; P G Hugenholtz; W Rafflenbeul; H Hecker; S Jost; J W Deckers
Journal:  Lancet       Date:  1990-05-12       Impact factor: 79.321

9.  Multicenter isradipine diuretic atherosclerosis study (MIDAS). Design features. The Midas Research Group.

Authors:  C D Furberg; R P Byington; N A Borhani
Journal:  Am J Med       Date:  1989-04-17       Impact factor: 4.965

10.  Verapamil suppresses atherosclerosis in cholesterol-fed rabbits.

Authors:  J L Rouleau; W W Parmley; J Stevens; J Wikman-Coffelt; R Sievers; R W Mahley; R J Havel
Journal:  J Am Coll Cardiol       Date:  1983-06       Impact factor: 24.094

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.