Schreiber V, Pribyl T
Physiol Bohemoslov. 1977;26(1):31-8.
Male and female rats were injected twice a week for three weeks with doses of 1 mg oestradiol benzoate (OE), were given perphenazine (P, 2 mg/rat/day) or the ergoline derivative D-6-methyl-8-ergoline-(I)-yl acetic acid amide (Deprenon SPOFA, D, 200 microng/rat/day) in their food or were treated with various combinations of all three factors. OE-induced adenohypophyseal growth was inhibited by D, but the inhibitory effect of D was completely suppressed by P. D also inhibited the OE-induced increase in the thyroxine-binding capacity of the adenohypophyseal proteins, but this inhibition was not suppressed by the simultaneous administration of P. The administration of OE was followed by elevation of the serum ceruloplasmin level, which was not inhibited by P or D, either alone or combined. Ovarian weight rose markedly after D and the increase was inhibited by the simultaneous administration of either OE or P.
对雄性和雌性大鼠每周注射两次剂量为1毫克苯甲酸雌二醇(OE),持续三周,在它们的食物中给予奋乃静(P,2毫克/大鼠/天)或麦角灵衍生物D - 6 - 甲基 - 8 - 麦角灵 -(I)- 基乙酸酰胺(Deprenon SPOFA,D,200微克/大鼠/天),或者用这三种因素的各种组合进行处理。D抑制了OE诱导的腺垂体生长,但D的抑制作用被P完全抑制。D还抑制了OE诱导的腺垂体蛋白质甲状腺素结合能力的增加,但同时给予P并不能抑制这种抑制作用。给予OE后血清铜蓝蛋白水平升高,单独或联合使用P或D均不能抑制。D给药后卵巢重量显著增加,同时给予OE或P可抑制这种增加。