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Atrial natriuretic factor (ANF), atrial natriuretic peptide (ANP) or atriopeptin, is a polypeptide hormone involved in the homeostatic control of body water and sodium. It is released by atrial myocytes, cells in the atria of the heart, in response to signals of raised blood pressure and acts to reduce this.

Structure


ANP is a 28 amino acid peptide with a 17 AA ring, and is closely related to BNP (Brain Natriuretic Peptide, but produced largely in the heart) and CNP (C-type Natriuretic Peptide) which all share the same amino acid ring. ANP was discovered in 1981 by a team in Ottawa led by Mercedes Kuroski de Bold after they made the seminal observation that injection of atrial (but not ventricular) tissue extracts into rats caused copious natriuresis.

Production


ANP is produced, stored and released by cells present in the atria of the heart, atrial myocytes. It is released in response to a variety of signals, the signals mostly being present when the subject is hypervolaemic.

It is secreted in response to:

Causes of stretching include high extracellular fluid volume, high blood volume, and atrial fibrillation. Notably, it is secreted in response to immersion of the body in water, which causes an atrial stretch due to altered distribution of intravascular fluid. It has been shown that in horses, it is also released in response to exercise.

Receptors


There are three distinct receptors identified so far in mammals, natriuretic peptide receptors A, B and C (NPRA, NPRB and NPRC).

NPRA and NPRB are linked to guanylyl cyclases, while NPRAC is G-protein linked and furthermore is a "clearance receptor" which acts to internalise and destroy the ligand.

Physiological effects


The overall effects of ANP release are a reduction in blood volume and therefore central venous pressure, cardiac output, and arterial blood pressure. It also increases renal sodium secretion and excretion.

The overall effect of which is to counter the blood pressure-raising effects of the renin-angiotensin system.

Renal

  • Dilates the afferent glomerular arteriole, constricts the efferent glomerular arteriole, and relaxes the mesangial cells. This increases the glomerular filtration rate, resulting in greater excretion of sodium and water.

  • Inhibits renin secretion.

Vascular

  • Relaxes vascular smooth muscle in arterioles and venules by:
    • Receptor-mediated elevation of vascular smooth muscle cGMP
    • Inhibition of the effects of catecholamines

Adrenal

Degradation


Degradation of ANP is needed for its actions to be stopped. It is broken down by an enzyme, neutral endopeptidase (NEP). Recently inhibitors of NEP have been developed, although have not yet been licenced, proving to be beneficial in congestive heart disease.

Other natriuretic factors


In addition to the mammalian natriuretic factors (ANP, BNP, CNP), two other peptides have been isolated. Tervonen (1998) described a salmon natriuretic factor (Salmon cardiac peptide) with a similar structure and properties and Dendroaspis Natriuretic Peptide (DNP) was discovered in the venom of the green mamba by Schweitz et al. (1992).

References


De Bold AJ 1985 Atrial natriuretic factor: a hormone produced by the heart. Science 230:767–770.

Joshi Venugopal, Pharmacological Modulation of the Natriuretic Peptide System, Expert Opinion in Therapuetic Patents, 2003, Vol. 13, No. 9, Pages 1389-1409.*

Clemo HF, Baumgarten CM, Stambler BS, Wood MA, Ellenbogen KA. Atrial natriuretic factor: implications for cardiac pacing and electrophysiology. PACE Pacing Clin Electrophysiol. 1994;17:70-91.

Tervonen et al., 1998 Endocrinology 139:4021-4025.

Kokkonen et al., 2000 Am J Physiol 278: E285-E292.

Peptide hormones | Cardiac hormones

Atriales natriuretisches Peptid | 心房性ナトリウム利尿ペプチド | Przedsionkowy peptyd natriuretyczny

 

This article is licensed under the GNU Free Documentation License. It uses material from the "Atrial natriuretic peptide".

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