Literature DB >> 15311086

Dihydropyridine calcium channel blockers: basic pharmacological similarities but fundamental therapeutic differences.

Peter A Meredith1, Henry L Elliott.   

Abstract

Recent trials indicate that treatment with calcium channel blockers (CCBs) reduces cardiovascular morbidity and mortality in hypertensive patients (including those with significant coronary artery disease). Since the fundamental mechanism of action of all CCBs is the same, it might be assumed that the findings of these outcome studies can be generalized to all types of CCB. However, in the light of the well-recognized clinical pharmacological differences between the 'rate-limiting' agents, verapamil and diltiazem, and the dihydropyridine group of CCBs, this must be considered to be a misconception. Less well-recognized, and often ignored, are the significant differences between agents within the dihydropyridine group. These differences translate to distinct differences in the therapeutic profiles and may well translate into differences in outcome during long-term treatment. Thus, the differences in pharmacokinetic, pharmacodynamic and therapeutic profiles make it clear that caution should be exercised in assuming that all dihydropyridine CCBs licensed for once-daily administration are equivalent in terms of their durations of action and overall antihypertensive efficacy.

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Year:  2004        PMID: 15311086     DOI: 10.1097/00004872-200409000-00002

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


  11 in total

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Authors:  Henry L Elliott; Peter A Meredith
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Review 5.  Modified-release nifedipine: a review of the use of modified-release formulations in the treatment of hypertension and angina pectoris.

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9.  Synthesis of Novel 4-[1-(4-fluorobenzyl)-5-imidazolyl] Dihydropyridines and Studying their Effects on Rat Blood Pressure.

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Review 10.  Open-loop static and dynamic characteristics of the arterial baroreflex system in rabbits and rats.

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Journal:  J Physiol Sci       Date:  2015-11-05       Impact factor: 2.781

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