Lei K Y, Yang M G, Oberleas D, Prasad A S
Proc Soc Exp Biol Med. 1975 Jun;149(2):417-21. doi: 10.3181/00379727-149-38819.
Oral contraceptive steroids, norethynodrel and mestranol, were fed to 11-wk-old female Sprague-Dawley rats, in combination and in quantities proportional to those used by women for contraceptive purposes. Three experiments were performed. The first experiment, demonstrated that 10 wk of treatment, impaired the animal's glucose tolerance, but not its insulin response to glucose. The second experiment demonstrated that 6 wk of steroid feeding, decreased the in vivo conversion of blood U-14C-labeled glucose into adipose tissue fatty acids and into diaphragm glycogen, although the effect on the diaphragm was not statistically significant. In the third experiment, it was found that the uptake of 2-deoxyglucose-1-14C by the adipose tissue removed from rats after 6 wk of treatment, was not different from that of control tissue, but the uptake by the hemidiaphragms was slightly lower.
将口服避孕甾体激素炔诺孕酮和炔雌醇甲醚,按女性避孕所用剂量比例混合后喂给11周龄的雌性斯普拉格-道利大鼠。共进行了三项实验。第一项实验表明,10周的治疗会损害动物的葡萄糖耐量,但不会影响其对葡萄糖的胰岛素反应。第二项实验表明,6周的甾体激素喂养会降低血液中U-14C标记葡萄糖在体内向脂肪组织脂肪酸和膈肌糖原的转化,尽管对膈肌的影响在统计学上不显著。在第三项实验中,发现治疗6周后从大鼠身上取下的脂肪组织对2-脱氧葡萄糖-1-14C的摄取与对照组织无异,但半膈肌的摄取略低。