Abstract
Apelin, a (neuro)vasoactive peptide, plays a prominent role in controlling body fluid homeostasis and cardiovascular functions. Experimental data performed in rodents have shown that apelin has an aquaretic effect via its central and renal actions. In the brain, apelin inhibits the phasic electrical activity of vasopressinergic neurons and the release of vasopressin from the posterior pituitary into the bloodstream and in the kidney, apelin regulates renal microcirculation and counteracts in the collecting duct, the antidiuretic effect of vasopressin occurring via the vasopressin receptor type 2. In humans and rodents, if plasma osmolality is increased by hypertonic saline infusion/water deprivation or decreased by water loading, plasma vasopressin and apelin are conversely regulated to maintain body fluid homeostasis. In patients with the syndrome of inappropriate antidiuresis, in which vasopressin hypersecretion leads to hyponatremia, the balance between apelin and vasopressin is significantly altered. In order to re-establish the correct balance, a metabolically stable apelin-17 analog, LIT01-196, was developed, to overcome the problem of the very short half-life (in the minute range) of apelin in vivo. In a rat experimental model of vasopressin-induced hyponatremia, subcutaneously (s.c.) administered LIT01-196 blocks the antidiuretic effect of vasopressin and the vasopressin-induced increase in urinary osmolality, and induces a progressive improvement in hyponatremia, suggesting that apelin receptor activation constitutes an original approach for hyponatremia treatment.
Highlights
Laboratory of Central Neuropeptides in the Regulation of Body Fluid Homeostasis and Cardiovascular Functions, Center for Interdisciplinary Research in Biology (CIRB), French National Institute for Health and Medical Research (INSERM), Unit U1050, National Center for Scientific Research (CNRS), Mixed Research Unit 7241, College de France, Paris, France
Various conditions have been associated with hyponatremia, including chronic heart failure, chronic kidney disease, liver cirrhosis, diuretic treatment and the Syndrome of Inappropriate Antidiuresis (SIAD), in which AVP secretion occurs in the absence of an osmotic or hemodynamic abnormality [93]
The identification of apelin as the endogenous ligand of the orphan receptor APJ constituted an important step in basic research, with clinical implications
Summary
The apelin story began in 1993 with the cloning of a cDNA for an orphan receptor, given the name “APJ receptor” (putative receptor protein related to the type 1 (AT1) angiotensin receptor) from a human genomic library [1]. This seven-transmembrane domain G-protein coupled receptor (GPCR) displays 31% amino-acid (aa) sequence identity to the human AT1 receptor and is encoded by a gene on chromosome 11. This 36-aa peptide was called apelin for APJ Endogenous LIgaNd, and the APJ receptor was renamed the apelin receptor (ApelinR)
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