Mechanisms acting against accumulation of volume are important in path
ophysiological situations with volume and salt overload, such as conge
stive heart failure. Osmoregulating animals that migrate between envir
onments with high and low salinity are ideal models for studying the d
efence mechanisms against volume gain. We have now cloned and sequence
d from salmon (Salmo salar) a cDNA encoding a novel vasorelaxant cardi
ac hormone of 29 amino acids which is produced by proteolytic processi
ng of a 148-residue preprohormone. Structural and biological results,
as well as its distribution indicate that it belongs to an unrecognize
d family related to natriuretic peptides, perhaps representing an ance
stor of ANP and BNP. We have synthesized the 29-amino acid hormone and
set up a specific radioimmunoassay. The distribution of the mRNA and
peptide is strictly restricted to the heart, with high levels both in
the atrium and ventricle in various fish species. The hormone relaxes
aortic smooth muscle derived from salmon at nanomolar concentrations.
Its release from isolated perfused salmon ventricle is very sensitive
to mechanical load: a 10 mmHg load induces a rapid 5-fold increase in
hormone release. Our results indicate that the novel cardiac hormone h
as an important role in fish volume regulation. They also demonstrate
that mechanical stimuli have been central to volume regulation since e
arly evolution.