On the use of Plasma Proteins as Indicators of the Metabolic Effects of Combined Oral Contraceptives
On the use of Plasma Proteins as Indicators of the Metabolic Effects of Combined Oral Contraceptives
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关于使用血浆蛋白作为复方口服避孕药代谢作用的指标
DOI:
10.3109/00016348209155359
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发表时间:
1982
影响因子:
4.3
通讯作者:
K. Stéffensen
中科院分区:
文献类型:
--
作者:
G. Cullberg;Per;G. Lindstedt;K. Stéffensen
Abstract. Ethinylestradiol (EE, 17α‐ethynyl‐1,3,5(10)‐es‐tratriene‐3,17β‐diol) 30 μg daily, in combination with 150μg per day of desogestrel (Org 2969,17α‐ethynyl‐18‐methyl‐11‐methylene‐4‐estrene‐17β‐ol) or levonorgestrel (17α‐ethynyl‐18‐methyl‐4‐estrene‐17β‐ol‐3‐one), was administered to two groups of 10 healthy human women who had been without hormonal treatment during 3 months prior to the study. The preparations were given for three 21‐day cycles with 7‐day intervals. Blood samples were taken before treatment and at the end of the third treatment period. Serum sex‐hormone binding globulin (SHBG), ceruloplasmin, ornsomucoid, C1‐esterase inhibitor and C4 were analyzed by electroimmunoassay and transcortin was assayed as cortisol‐binding capacity. Serum testosterone was assayed by radioimmunoassay of methylenedichloride extracts using an antiserum with about 20% cross‐reactivity for dihydrotestosterone (DHT).