Lloyd H M, Jacobi J M, Meares J D
J Endocrinol. 1978 Apr;77(1):129-36. doi: 10.1677/joe.0.0770129.
Haloperidol, bromocriptine and diethylstilboestrol dipropionate were given in various régimes to male rats to determine their effects on pituitary DNA synthesis, prolactin secretion and growth hormone secretion. Haloperidol increased serum prolactin but did not stimulate pituitary DNA synthesis or reduce pituitary prolactin concentrations. Haloperidol potentiated the effects of oestrogen on serum prolactin and on pituitary DNA synthesis; pituitary prolactin concentrations were greatly reduced, and growth hormone secretion was slightly inhibited. The inhibitory effects of bromocriptine in oestrogen-stimulated rats were demonstrated by smaller pituitary weights and decreased DNA synthesis; serum prolactin levels were lowered and pituitary prolactin concentrations were increased. Haloperidol, given to rats treated with oestrogen and bromocriptine, reversed the inhibitory effects of bromocriptine on DNA synthesis and serum prolactin; pituitary prolactin concentrations fell to well below normal. The results suggest that the haloperidol potentiation of oestrogen-induced pituitary DNA synthesis may depend upon stimulation of prolactin secretion together with reduction of intracellular prolactin levels.
将氟哌啶醇、溴隐亭和己烯雌酚二丙酸酯以不同方案给予雄性大鼠,以确定它们对垂体DNA合成、催乳素分泌和生长激素分泌的影响。氟哌啶醇可增加血清催乳素水平,但不刺激垂体DNA合成,也不降低垂体催乳素浓度。氟哌啶醇增强了雌激素对血清催乳素和垂体DNA合成的作用;垂体催乳素浓度大幅降低,生长激素分泌略有抑制。溴隐亭对雌激素刺激的大鼠的抑制作用表现为垂体重量减轻和DNA合成减少;血清催乳素水平降低,垂体催乳素浓度升高。给用雌激素和溴隐亭治疗的大鼠注射氟哌啶醇,可逆转溴隐亭对DNA合成和血清催乳素的抑制作用;垂体催乳素浓度降至远低于正常水平。结果表明,氟哌啶醇增强雌激素诱导的垂体DNA合成可能取决于催乳素分泌的刺激以及细胞内催乳素水平的降低。