The etiology of hepatorenal syndrome is still incompletely understood,
but the nonosmotic release of arginine vasopressin (AVP) seems to hav
e an important role. Since AVP presents a well-defined daily periodici
ty in its production and secretion, the aim of the study was to invest
igate the circadian rhythm in its circulating plasma concentrations in
patients with hepatorenal syndrome, compared with healthy controls. V
enous blood samples were drawn during a 24 hour period at 2 hourly int
ervals from a peripheral vein in 10 healthy subjects and in 10 patient
s with hepatorenal syndrome for the determination of the circulating p
lasma levels of AVP by radioimmunoassay. Statistical analysis was carr
ied out by the 'cosinor' method. The controls presented a significant
(p < 0.002) circadian rhythm in the AVP circulating levels, whereas no
rhythm (p > 0.05) was found in patients. The circadian rhythms were s
ignificantly (p < 0.005) different between the two groups, patients ha
ving higher mean daily concentration and lower circadian variation of
AVP. These results confirm the existence of a well-defined circadian r
hythm of AVP in healthy subjects, whereas the hepatorenal syndrome pat
ients present a complete loss of the circadian rhythm. It could be hyp
othesized that primitive damage in circadian time-keeping regulates th
e circadian rhythm of vasopressinergic neurons, or has a secondary eff
ect on the peripheral vasodilatation in the course of advanced liver d
isease. This great upset in the temporal and functional organization,
together with that of the renin-angiotensin-aldosterone system, could
play an important role in promoting and/or in the maintenance of the h
ydroelectrolyte imbalance that characterizes the hepatorenal syndrome.