EFFECTS OF BROMOCRIPTINE ON SERUM PROLACTIN LEVELS, PITUITARY WEIGHT AND IMMUNOREACTIVE PROLACTIN CELLS IN ESTRADIOL-TREATED OVARIECTOMIZEDRATS - AN EXPERIMENTAL-MODEL OF ESTROGEN-DEPENDENT HYPERPROLACTINEMIA
Mf. Ribeiro et al., EFFECTS OF BROMOCRIPTINE ON SERUM PROLACTIN LEVELS, PITUITARY WEIGHT AND IMMUNOREACTIVE PROLACTIN CELLS IN ESTRADIOL-TREATED OVARIECTOMIZEDRATS - AN EXPERIMENTAL-MODEL OF ESTROGEN-DEPENDENT HYPERPROLACTINEMIA, Brazilian journal of medical and biological research, 30(1), 1997, pp. 113-117
The present study was designed to assess the effects of bromocriptine,
a dopamine agonist, on pituitary wet weight, number of immunoreactive
prolactin cells and serum prolactin concentrations in estradiol-treat
ed rats. Ovariectomized Wistar rats were injected subcutaneously with
sunflower oil vehicle or estradiol valerate (50 or 300 mu g rat(-1) we
ek(-1)) for 2, 4 or 10 weeks, Bromocriptine (0.2 or 0.6 mg rat(-1) day
(-1)) was injected daily during the last 5 or 12 days of estrogen trea
tment. Data were compared with those obtained for intact control rats.
Administration of both doses of estrogen increased serum prolactin le
vels. No difference in the number of prolactin cells in rats treated w
ith 50 mu g estradiol valerate was observed compared to intact adult a
nimals. In contrast, rats treated with 300 mu g estradiol valerate sho
wed a significant increase in the number of prolactin cells (P<0.05).
Therefore, the increase in serum prolactin levels observed in rats tre
ated with 50 mu g estradiol valerate, in the absence of morphological
changes in the pituitary cells, suggests a ''functional'' estrogen-ind
uced hyperprolactinemia. Bromocriptine decreased prolactin levels in a
ll estrogen-treated rats. The administration of this drug to rats prev
iously treated with 300 mu g estradiol valerate also resulted in a sig
nificant decrease in pituitary weight and number of prolactin cells wh
en compared to the group treated with estradiol alone. The general ant
iprolactinemic and antiproliferative pituitary effects of bromocriptin
e treatment reported here validate the experimental model of estrogen-
induced hyperprolactinemic rats.