Literature DB >> 2973331

The atrial peptide system in cardiac disease.

J C Burnett1.   

Abstract

Atrial natriuretic factor (ANF) is a peptide hormone of cardiac origin, released in response to atrial distention, that increases sodium excretion, inhibits the renin-angiotensin-aldosterone (RAA) system, and decreases arterial pressure. Congestive heart failure (CHF) is a clinical syndrome that is characterized by chronic atrial distention, sodium retention with edema, and activation of the RAA system. The role of ANF in the pathophysiology of CHF remains to be defined. Circulating ANF is greatly increased in congestive heart failure. The mechanism of this elevation of ANF is explained by increased synthesis and release of ANF from the atria with atrial depletion of ANF in response to chronic atrial overload. Recent work also suggests the presence of ANF in ventricular myocardium in heart failure in which the ventricle is recruited to synthesize and release this peptide hormone. Despite increased circulating ANF in heart failure, the kidney retains sodium and is hyporesponsive to exogenous administration of ANF. The mechanism of this hyporesponsiveness is multifactorial but may be explained in part by activation of the intrarenal RAA system as well as by a reduction in renal perfusion pressure. A therapeutic role for ANF remains unclear. To date, studies conflict, but some investigations of ANF infusions in man support a unique and selective renal vasodilator action in association with an ability to inhibit the RAA system.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 2973331     DOI: 10.1093/ajh/1.4.410s

Source DB:  PubMed          Journal:  Am J Hypertens        ISSN: 0895-7061            Impact factor:   2.689


  4 in total

1.  Release of atrial natriuretic factor after pericardiocentesis for malignant pericardial effusion.

Authors:  D B Northridge; J McMurray; S Ray; A Jardine; H J Dargie
Journal:  BMJ       Date:  1989-09-02

Review 2.  Natriuretic peptides and the genomics of left-ventricular hypertrophy.

Authors:  Daniel L Dries
Journal:  Heart Fail Clin       Date:  2010-01       Impact factor: 3.179

3.  Simultaneous assessment of unprocessed ProBNP1-108 in addition to processed BNP32 improves identification of high-risk ambulatory patients with heart failure.

Authors:  Daniel L Dries; Bonnie Ky; Alan H B Wu; J Eduardo Rame; Mary E Putt; Thomas P Cappola
Journal:  Circ Heart Fail       Date:  2010-01-27       Impact factor: 8.790

Review 4.  Clinical impact of renin-angiotensin system blockade: angiotensin-converting enzyme inhibitors vs. angiotensin receptor antagonists.

Authors:  Joseph L Izzo; Marvin Moser
Journal:  J Clin Hypertens (Greenwich)       Date:  2002 Nov-Dec       Impact factor: 3.738

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.