The shift in the "paradigm" of the pharmacology of hypertension.

Abstract

Until recently elevated blood pressure was considered as a hemodynamic entity representing an increase in workload for the heart and the arterial tree. Control of hypertension meant hemodynamic unloading, through inhibition of vasoconstrictor pathways, principally renin-angiotensin system and sympathetic system. In recent years however a new pharmacological approach has evolved as a result of (i) the dissociation of endothelial dysfunction and vascular pathology from increased blood pressure; (ii) the recognition that endothelial dysfunction regards not only the vascular reactivity, but also promotes atherosclerosis and thrombosis; and (iii) an improved understanding of the complexity of local-tissue renin angiotensin system and of the vasodilatory and cytoprotective role of natriuretic peptides. This has led to a reconsideration of existing medicines in terms of specification on endothelial function, more rationalized application of drugs and search for new compounds targeting both vasodilatory and anti-proliferative pathways. Examples include beta1-adrenergic antagonists, such as Nebivolol and Carvedilol, and vasopeptidase inhibitors, such as Omapatrilat, that inhibit simultaneously the angiotensin converting enzyme and neutral endopeptidase. Furthermore the identification of genetic polymorphisms in the effectors involved in the pathophysiology of hypertension or in the response to anti-hypertensive drugs, such as the p22phox subunit of NADPH oxidase, alpha-adducin or adrenergic receptors, has promoted the prospective of both better understanding of hypertension and individualized strategies for its treatment.

• Authors: Christodoulos S Flordellis, Dimitrios Goumenos, George Kourounis, Sotirios A Tsementzis, Hervé Paris, Jaannis Vlachojiannis
• Journal: Current topics in medicinal chemistry (Curr Top Med Chem) Vol. 4 Issue 4 Pg. 487-98 ( 2004) ISSN: 1568-0266 [Print] United Arab Emirates
• PMID: 14965315 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)

Chemical References

• Adrenergic beta-Antagonists
• Angiotensins
• Antihypertensive Agents
• GTP-Binding Proteins

Topics

• Adrenergic beta-Antagonists (pharmacology)
• Angiotensins (metabolism)
• Antihypertensive Agents (adverse effects, pharmacology, therapeutic use)
• Cardiovascular System (metabolism)
• Endothelium (drug effects, metabolism)
• GTP-Binding Proteins (metabolism)
• Humans
• Hypertension (drug therapy, genetics, metabolism)
• Pharmacogenetics
• Renin-Angiotensin System (drug effects)
• Vasculitis (metabolism)