RESPONSIVENESS OF THE GLUCOCORTICOID-SUPPRESSED PITUITARY-ADRENOCORTICAL SYSTEM OF PIGEONS (COLUMBA-LIVIA DOMESTICA) TO STIMULATION WITH ARGININE-VASOPRESSIN
I. Westerhof et al., RESPONSIVENESS OF THE GLUCOCORTICOID-SUPPRESSED PITUITARY-ADRENOCORTICAL SYSTEM OF PIGEONS (COLUMBA-LIVIA DOMESTICA) TO STIMULATION WITH ARGININE-VASOPRESSIN, Avian diseases, 40(2), 1996, pp. 312-320
This paper reports on the duration of the suppressive effects of singl
e high and low doses of dexamethasone, cortisol, and prednisolone on t
he pituitary-adrenocortical (PA) system in pigeons. Tn addition, the e
ffects of long-term daily administration of a high dose of dexamethaso
ne are reported. In Expt. 1, low and high doses of dexamethasone (0.5
mu g/kg and 0.5 mg/kg), cortisol (15 mu g/kg and 1.5 mg/kg), and predn
isolone (3.5 mu g/kg and 3.5 mg/kg)were administered around tile expec
ted nadir (4 hr before the peak) of the diurnal plasma corticosterone
concentration. The recovery of the PA system was investigated by measu
ring plasma corticosterone concentrations before and 30 min after argi
nine vasopressin (AVP) stimulation (10 mu g/kg) around the expected pe
ak of plasma corticosterone concentrations. In Expt. 2, one high dose
of each of the three glucocorticoids was administered 4 hr before the
peak, followed by AVP stimulation around the expected peak of plasma c
orticosterone concentrations each day for 3 days. In Expt. 3, the reco
very of the PA system following long-term daily administration of 1 mg
/kg dexamethasone was investigated by repeated stimulations with AVP a
fter cessation of the treatment. The results of these experiments (I)
confirm that the PA system of pigeons is very sensitive to the suppres
sive effects of dexamethasone, cortisol, and prednisolone in a dose-de
pendent manner, (II) demonstrate that after cessation of glucocorticoi
d treatment the response to AVP stimulation is restored earlier than b
asal corticosterone concentrations, (III) demonstrate thar after long-
term glucocorticoid treatment the responsiveness of the PA system reco
vers relatively fast, and (IV) demonstrate that long-term treatment wi
th a high dose of dexamethasone not only results in complete suppressi
on of the PA system but is also a serious risk for infection and death
.