Literature DB >> 6241624

Regression of structural cardiovascular changes by antihypertensive therapy in spontaneously hypertensive rats.

S A Lundin, M I Hallbäck-Nordlander.   

Abstract

Trophic adrenergic influences may in part potentiate the pressure dependent development of structural cardiovascular changes in hypertension. Regression of such changes by antihypertensive treatment should therefore be most successful if adrenergic blocking drugs are used. In the present study spontaneously hypertensive rats (SHR) received either alpha-methyldopa, metoprolol, felodipine, a new vasodilating Ca2+-antagonist, or metoprolol and felodipine in combination for 10 weeks. Their left ventricles were weighed and resistance vessel design was analysed using a haemodynamic technique. Arterial pressure (MAP) was equally reduced by metoprolol and felodipine. Despite their different modes of action cardiovascular design was also equally affected. The combined regimen reduced average MAP more than either drug alone. It also caused more pronounced regression of cardiovascular structural changes. Methyldopa lowered MAP less than either metoprolol or felodipine and had only modest effects on cardiovascular design. Thus, the extent of MAP reduction, regardless of which therapeutic regimen is used to induce it, determines the extent of regression of structural cardiovascular changes during antihypertensive treatment.

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Year:  1984        PMID: 6241624     DOI: 10.1097/00004872-198402000-00003

Source DB:  PubMed          Journal:  J Hypertens        ISSN: 0263-6352            Impact factor:   4.844


  8 in total

Review 1.  The effects of treatment on target organ damage in hypertensive disease.

Authors:  J Lowenstein
Journal:  Postgrad Med J       Date:  1985-09       Impact factor: 2.401

2.  Haemodynamic effects of short and long term administration of felodipine in spontaneously hypertensive rats.

Authors:  M Nordlander
Journal:  Drugs       Date:  1985       Impact factor: 9.546

Review 3.  Changes to the vascular system resulting from hypertension and their effects on response to therapy.

Authors:  M J Mulvany
Journal:  Drugs       Date:  1990       Impact factor: 9.546

Review 4.  'Second generation' dihydropyridine calcium antagonists. Greater vascular selectivity and some unique applications.

Authors:  D D Freedman; D D Waters
Journal:  Drugs       Date:  1987-11       Impact factor: 9.546

Review 5.  Pharmacodynamic properties of felodipine.

Authors:  B Ljung; M Nordlander
Journal:  Drugs       Date:  1987       Impact factor: 9.546

6.  Prevention of hypertensive hypertrophy by medical therapy: effects on systolic wall stress and systolic function.

Authors:  W Motz; B E Strauer
Journal:  Basic Res Cardiol       Date:  1985 Nov-Dec       Impact factor: 17.165

7.  Reduction by oral propranolol treatment of left ventricular hypertrophy secondary to pressure-overload in the rat.

Authors:  I Ostman-Smith
Journal:  Br J Pharmacol       Date:  1995-11       Impact factor: 8.739

Review 8.  Factors involved in the pathogenesis of hypertensive cardiovascular hypertrophy. A review.

Authors:  B Dahlöf
Journal:  Drugs       Date:  1988       Impact factor: 9.546

  8 in total

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