Carrington L J, Bailey C J
Horm Res. 1985;21(3):199-203. doi: 10.1159/000180045.
Glycogen deposition and glucose tolerance were examined in female mice after 24 days of oral treatment with natural (17 beta-estradiol and progesterone) and synthetic (ethinyl estradiol and norethisterone acetate) sex steroids, administered individually and in estrogen-progestin combination. Doses were 5 micrograms/kg/day for estrogens and 1 mg/kg/day for progestins. Compared with diestrus control mice, each treatment increased glycogen deposition in liver, uterus, heart and biceps femoris muscle. 17 beta-Estradiol produced the greatest increments. Progesterone produced considerably smaller increments and antagonized the glycogenic effects of 17 beta-estradiol. Ethinyl estradiol and norethisterone acetate generally induced similar changes in glycogen deposition. Treatments containing 17 beta-estradiol improved glucose tolerance. Although glucose tolerance was not significantly altered by the other sex steroid treatments, the changes in glycogen deposition indicate important effects on tissue carbohydrate metabolism.
在用天然(17β-雌二醇和孕酮)和合成(炔雌醇和醋酸炔诺酮)性类固醇进行24天口服治疗后,对雌性小鼠的糖原沉积和葡萄糖耐量进行了检测,这些性类固醇单独给药以及以雌激素 - 孕激素组合给药。雌激素剂量为5微克/千克/天,孕激素剂量为1毫克/千克/天。与动情后期对照小鼠相比,每种治疗均增加了肝脏、子宫、心脏和股二头肌中的糖原沉积。17β-雌二醇产生的增量最大。孕酮产生的增量小得多,并拮抗17β-雌二醇的糖原生成作用。炔雌醇和醋酸炔诺酮通常在糖原沉积方面诱导相似的变化。含有17β-雌二醇的治疗改善了葡萄糖耐量。虽然其他性类固醇治疗未显著改变葡萄糖耐量,但糖原沉积的变化表明对组织碳水化合物代谢有重要影响。