An endogenous serotonergic rhythm acting on 5-HT2A receptors may be involved in the diurnal changes in tuberoinfundibular dopaminergic neuronal activity and prolactin secretion in female rats
Sl. Liang et Jt. Pan, An endogenous serotonergic rhythm acting on 5-HT2A receptors may be involved in the diurnal changes in tuberoinfundibular dopaminergic neuronal activity and prolactin secretion in female rats, NEUROENDOCR, 72(1), 2000, pp. 11-19
The central serotonergic system has long been known to have a stimulatory r
ole on the secretion of prolactin (PRL). The integrity of serotonergic neur
otransmission is essential for the expression of the estrogen-induced after
noon PRL surge. Whether its effect on PRL involves change in the activity o
f tuberoinfundibular dopaminergic (TIDA) neurons has not been ascertained.
in adult ovariectomized rats treated with estrogen, depletion of central se
rotonin (5-HT) by 5,7-dihydroxytryptamine (5,7-DHT, 200 mu g/rat, i.c.v.) e
ffectively prevented the afternoon fall in TIDA neuronal activity (using th
e levels of 3,4-dihydroxyphenylalanine and 3,4-dihydroxyphenyl-acetic acid
(DOPAC), and the ratio of DOPAC/dopamine in the median eminence as indices)
, and blunted the afternoon PRL surge. A single injection of a 5-HT2A recep
tor antagonist, ketanserin (5 mg/kg, i.p. at 12.00 h), also had the same ef
fects on the diurnal changes in TIDA neuronal activity and PRL secretion as
the treatment with 5,7-DHT did. Intracerebroventricular injection of a 5-H
T2 receptor agonist 2,5-dimethoxy-4-iodoamphetamine (DOI) in the morning in
hibited the TIDA neuronal activity and stimulated PRL secretion in a dose-d
ependent manner; while injection of a 5-HT1 agonist, 8-hydroxy-dipropylamin
otetralin, was without effect. Injection of DOI in 5,7-DHT-pretreated rats
at 14.30 h also lowered the TIDA neuronal activity and reinstated the PRL s
urge. In all, endogenous 5-HT, acting through the 5-HT2A receptor, appears
to exhibit an inhibitory effect on TIDA neuronal activity during the aftern
oon, which is essential for the PRL surge. copyright (C) 2000 S. Karger AG,
Basel.