Chapman A J, MacFarlane I A, Shalet S M, Beardwell C G, Dutton J, Sutton M L
Clin Endocrinol (Oxf). 1984 Aug;21(2):123-9. doi: 10.1111/j.1365-2265.1984.tb03451.x.
We have studied a women who presented at the age of 51 with a large FSH and alpha-subunit producing pituitary adenoma. Following insertion of ventriculo-peritoneal shunts and external pituitary irradiation there was no change in the elevated serum concentrations of FSH, and alpha-subunit over a four year period although she developed both ACTH and TSH deficiency. Various drugs, however, did alter the FSH and alpha-subunit concentrations and these changes suggest possible mechanisms controlling FSH secretion. Ethinyloestradiol 0.03 mg daily for three weeks suppressed serum FSH to 77% of the basal level (240 +/- 35 i.u./l to 184 +/- 20 i.u./l) but alpha-subunit rose to 130% of basal level (281 +/- 50 ng/ml to 366 +/- 40 ng/ml). On ethinyloestradiol 0.1 mg daily, FSH suppressed to 17% of basal (40 +/- 11 i.u./l) with no change in alpha-subunit concentration, while on 0.2 mg daily suppression of FSH was similar but alpha-subunit fell to 59% of basal (190 +/- 28 ng/ml). Dexamethasone, 3 mg daily for one week reduced FSH to 53% of the initial concentration and alpha-subunit to 74% while bromocriptine 7.5 mg daily for three months, reduced FSH to 39% and alpha-subunit to 66% of basal. Neither thyroxine, 0.2 mg daily for four weeks, nor an LHRH analogue, (Buserelin, Hoechst) 200 micrograms, three times daily for three months elicited any effect. Chromatography on Sephadex G100 showed that serum FSH and alpha-subunit both had Kav values somewhat lower than those of their standard counterparts (FSH, 0.20 vs 0.25; alpha-subunit 0.35 vs 0.45).(ABSTRACT TRUNCATED AT 250 WORDS)
我们研究了一位51岁的女性,她患有分泌促卵泡生成素(FSH)和α亚基的大型垂体腺瘤。在植入脑室-腹腔分流管并进行垂体外部照射后,尽管她出现了促肾上腺皮质激素(ACTH)和促甲状腺激素(TSH)缺乏,但在四年时间里,血清FSH和α亚基的升高浓度并未改变。然而,各种药物确实改变了FSH和α亚基的浓度,这些变化提示了控制FSH分泌的可能机制。每天服用0.03毫克乙炔雌二醇,持续三周,血清FSH降至基础水平的77%(从240±35国际单位/升降至184±20国际单位/升),但α亚基升至基础水平的130%(从281±50纳克/毫升升至366±40纳克/毫升)。每天服用0.1毫克乙炔雌二醇,FSH降至基础水平的17%(40±11国际单位/升),α亚基浓度无变化,而每天服用0.2毫克时,FSH的抑制情况相似,但α亚基降至基础水平的59%(190±28纳克/毫升)。每天服用3毫克地塞米松,持续一周,FSH降至初始浓度的53%,α亚基降至74%,而每天服用7.5毫克溴隐亭,持续三个月,FSH降至基础水平的39%,α亚基降至66%。每天服用0.2毫克甲状腺素,持续四周,以及每天三次,每次200微克的促性腺激素释放激素(LHRH)类似物(布舍瑞林,赫斯特公司),持续三个月,均未产生任何效果。在Sephadex G100上进行色谱分析表明,血清FSH和α亚基的分配系数(Kav)值均略低于其标准对应物(FSH,0.20对0.25;α亚基,0.35对0.45)。(摘要截断于250字)