Abstract
Control of blood pressure in hypertension has generally been achieved in the past by the use of diuretics and betablockers, either alone or in combination with vasodilators or drugs interacting with the sympathetic nervous system. These treatments obviously have highly beneficial effects since several controlled trials have shown that lowering of blood pressure reduces cardiovascular mortality and morbidity in treated hypertensive patients. (Australian Therapeutic Trial of Mild Hypertension 1980; Smith 1977; Veterans Administration Cooperative Study Group 1970). There are, however, some limitations in this approach to the treatment of hypertension. In approximately two thirds of unselected patients, satisfactory control of blood pressure is not obtained with the drug of first choice alone. Therefore it is often necessary to prescribe two or more drugs. The antihypertensive effect of diuretics can be limited by overstimulation of the renin-angiotensin system (Alhenc-Gelas et al. 1978; Laragh 1973) and that of vasodilators by sodium retention (Ibsen et al. 1978). Side-effects such as postural hypotension, disturbance of the microcirculation or erectile dysfunction are not uncommon (Smith 1977). Recently, two new classes of antihypertensive agent: converting enzyme inhibitors and calcium channel blockers, became available for the treatment of hypertension (Table 1). Although their mechanisms of action vary they are all able to decrease vascular resistance and lower blood pressure in patients with mild to severe hypertension.
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References
Aldigier JC, Plouin PF, Alexandre JM, Corvol P, Menard J (1981) Dose dependency of Captopril effects in severely hypertensive patients. J Cardiovasc Pharmacol 3:1229–1235.
Aldigier JC, Plouin PF, Guyene TT, Thibonnier M, Corvol P, Menard J (1982) Comparison of the hormonal and renal effects of Captopril in severe essential and renovascular hypertension. Am J Cardiol 49:1447–1452.
Alhenc-Gelas F, Plouin P-F, Ducrocq M-B, Corvol P, Menard J (1978) Comparison of the antihypertensive and hormonal effects of a cardioselective beta-blocker, acebutolol, and diuretics in essential hypertension. Am J Med 64:1005–1012.
Aoki K, Kondo Mochizaki A, Yoshida T, Kato S, Kato K, Takiwawa K (1978) Antihypertensive effect of Ca2 + antagonist in hypertensive patients in the absence and presence of beta adrenergic blockage. Am Heart J 96:218–226.
Atlas SA, Case DB, Sealey JE, Laragh JH, McKinstry DN (1979) Interruption of the renin-angiotensin system in hypertensive patients by Captopril induces sustained reduction in aldosterone secretion, potassium retention and natriuresis. Hypertension 1:274–280.
Australian Therapeutic Trial in mild hypertension. Report by the Management Committee (1980) Lancet i: 1261–1267.
Bertel O, Conen D, Radu EW, Muller J, Lang C, Dubach UC (1983) Nifedipine in hypertensive emergencies. Br Med J 286:19–21.
Bühler FR, Hulthén UL, Kiowski W, Müller FB, Bolli P (1982) The place of the calcium antagonist verapamil in antihypertensive therapy. J Cardiovasc Pharmacol 4: S350–S357.
Case DB, Atlas SA, Laragh JH, Sullivan PA, Sealey JE (1980) Use of first-dose response or plasma renin activity to predict the long term effect of Captopril: identification of triphasic pattern of blood pressure response. J Cardiovasc Pharmacol 2:339–346.
Clauser E, Genain C, Bouhnik, Corvol P, Menard J (1982) Variations de l’angiotensinogene et du des-angiotensine I-angiotensinogene chez l’homme et le rat au cours de l’inhibition de l’enzyme de conversion. Arch Mal Coeur n° Special; 157–161.
Cody RJ, Burton J, Evin G, Poulsen K, Herd JA, Haber E (1980) A substrate analog inhibitor of renin that is effective in vivo. Biochem Biophys Res Commun 97:230–235.
Cushman DW, Cheung HS, Sabo EF, Ondetti MA (1977) Design of potent competitive inhibitors of angiotensin-converting enzyme. Biochemistry 16:5484–5491.
Erdos EG (1976) Conversion of angiotensin I to angiotensin II. Am J Med 60:749–759.
Fagard R, Amery A, Lijnen P, Reybrouck T (1979) Haemodynamic effects of Captopril in hypertensive patients comparison with saralasin. Clin Sci 57:131S–134S.
Ferguson RK, Brunner HR, Turini GA, Gavras H, McKinstry DN (1977) A specific orally active inhibitor of angiotensin converting enzyme in man. Lancet i: 775–778.
Gardes J, Evin G, Castro B, Corvol P, Menard J (1980) Synthesis and renin inhibitory properties of a new soluble pepstatin derivative. J Cardiovasc Pharmacol 2:687–698.
Heel RC, Brodgen RN, Speight TM, Avery GS (1980) Captopril: a preliminary review of its pharmacological properties and therapeutic efficacy. Drugs 20:409–452.
Huang CM, Saloman J, Molteni A, Quintanilla A, De Greco F (1980) Antihypertensive effect of Captopril and propranolol. Clin Pharmacol Ther 27:258–259.
Ibsen H, Rasmussen K, Jensen HAE, Leth A (1978) Changes in plasma volume and extracellular fluid volume after addition of hydralazine to propranolol in patients with hypertension. Acta Med Scand 203:419–423.
Jenkins AC, MacKinstry DN (1979) Review of clinical studies of hypertensive patients treated with Captopril. Med J Aust 2: (Suppl 2) xxxii–xxxvii.
Laragh JH (1973) Vasoconstriction volume analysis for understanding and treating hypertension. The use of renin and aldosterone profiles. Am J Med 55:261–274.
Lederballe Petersen O, Christensen NJ, Rämsch KD (1980) Comparison of acute effects of nifedipine in normotensive and hypertensive man. J Cardiovasc Pharmacol 2:357–366.
Levenson J, Simon A, Tremmar M, Safar M (1980) Action antihypertensive du Captopril: etude hemdynamique. Nouv Presse Med 9:617–619.
Lewis GRJ, Stewart DJ, Lewis BM, Bones PJ, Morley KD, Janus ED (1981) The antihypertensive effect of oral verapamil. Acute and long term administration and its effects on the high density lyoprotein values in plasma. In: Zanchetti and Kreber (eds) Calcium antagonism in cardiovascular therapy. Experience with verapamil. Excerpta Medica, Amsterdam-Oxford-Princetown 270–277.
MacGregor GA, Markander ND, Roulston JA, Jones JC, Morton JJ (1981) The renin angiotensin system: a normal mechanism for maintaining blood pressure in normotensive and hypertensive subjects. In: Angiotensin converting enzyme inhibitors Morowitz ZP (ed) Urban and Swarzenberg-Baltimore 329–349.
MacGregor GA, Markandu ND, Banks RA, Bayliss J, Rouston JE, Jones JC (1982a) Captopril in essential hypertension contrasting effects of adding hydrochlorothiazide or propranolol. Br Med J 284:693–698.
MacGregor GA, Rotellar C, Markandu ND, Smith SS, Sagnella GA (1982b) Contrasting effects of nifedipine, Captopril and propranolol in normotensive and hypertensive subjects. J Cardiovasc Pharmacol 4 (Suppl 3):S358–S362.
Maeda K, Takasugi T, Tsukano Y, Tanaka Y, Shiota K (1981) Clinical study on the hypertensive effect of diltiaziem hydrochloride. Int J Clin Pharmacol Therap Toxic 19:47–55.
Mimran A, Brunner HR, Turini GA, Waeber B, Brunner D (1979) Effect of Captopril on renal vascular tone in patients with essential hypertension. Clin Sci 57:421S–432S
Muiesan G, Abigiti-Rosei E, Alicandri C, Bescki M, Castercano M, Corea L, Fariello R, Romanelli G, Pasini C, Platto L (1981) Influence of verapamil on catecholamines renin and aldosterone in essential hypertensive patients. In: Zanchetti and Krikler (eds) Calcium antagonism in cardiovascular therapy. Experience with verapamil. Excerpta Medica, Amsterdam-Oxford-Princeton 238–249.
Olivart MT, Bartorelli C, Polese A, Fiorentini O, Moruzzi P, Guazzi MD (1979) Treatment of hypertension with nifedipine, a calcium antagonistic agent. Circulation 59:1056–1062.
Soto ME, Thibonnier M, Sire O, Menard J, Corvol P, Milliez P (1981) Antihypertensive and hormonal effects of single oral doses of Captopril and nifedipine in essential hypertension. Eur J Clin Pharmacol 20:157–161.
Spivack C, Ocken S, Frishman WH (1983) Calcium antagonists: clinical use in the treatment of systemic hypertension. Drugs: 25:154–177.
Triggle DJ, Swamy VC (1983) Calcium antagonists: some chemical-pharmacologic aspects. Circ Res 52 (Suppl 1): 17–28.
Patchett AA, Harris E, Tristram E, et al. (1981) A new class of angiotensin — converting enzyme inhibitors. Nature 288:280–283.
Smith WM (1977) US Public Health Service Hospitals Cooperative Study Group. Treatment of mild hypertension. Results of ten year intervention trial. Circ Res 40 (Suppl i): 98–105.
Veterans Administration Cooperative Study Group on antihypertensive agents. Effects of treatment on morbidity in hypertension. Results in patients with diastolic blood pressure averaging 90 through 114 mm Hg. JAMA 213 C: 1143–1152.
Weinberger MH (1980) Angiotensin converting enzyme (ACE 1) inhibition in treatment of resistant hypertension. Clin Pharmacol Ther 27:293.
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© 1984 Dr. Dietrich Steinkopff Verlag, GmbH & Co. KG, Darmstadt
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Alhenc-Gelas, F., Corvol, P., Menard, J. (1984). New pharmacological approaches in the treatment of mild hypertension. The potential role of converting enzyme inhibitors and calcium blocking agents. In: Weber, M.A., Mathias, C.J. (eds) Mild hypertension. Steinkopff. https://doi.org/10.1007/978-3-642-87506-9_13
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DOI: https://doi.org/10.1007/978-3-642-87506-9_13
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