Department of Endocrinology, Ghent University Hospital, Ghent, Belgium.
Diabetes Care. 2010 Aug;33(8):1831-3. doi: 10.2337/dc10-0515. Epub 2010 May 18.
To evaluate metabolic effects of sex steroids in nonfasting and fasting conditions, independent from changes in body composition.
A randomized clinical trial was performed to create contrasting sex steroid levels in healthy young men: by letrozole (aromatase inhibitor) to lower estradiol (E(2)) and increase testosterone (group T, n = 10) versus letrozole plus E(2) patches to lower T and raise E(2) (group E, n = 10). Mixed meals and hyperinsulinemic-euglycemic clamps were performed before and after a 1-week treatment period.
Following intervention, the postprandial triglyceride response displayed a diverging response with a decline in group T and an increase in group E; the postprandial glucose-dependent insulinotropic polypeptide (GIP) response increased in group T. Insulin sensitivity increased in group T but remained unaltered in group E.
In healthy young men, short-term changes in sex steroids affect postprandial triglyceride and GIP response and insulin sensitivity.
评估非禁食和禁食条件下性激素对代谢的影响,而不受身体成分变化的影响。
进行了一项随机临床试验,以在健康年轻男性中产生对比性激素水平:通过来曲唑(芳香酶抑制剂)降低雌二醇(E(2))并增加睾丸激素(组 T,n = 10),与来曲唑加 E(2)贴片降低睾丸激素并提高 E(2)(组 E,n = 10)。在治疗前和治疗后 1 周进行混合餐和高胰岛素-正葡萄糖钳夹。
干预后,餐后甘油三酯反应显示出不同的反应,组 T 下降,组 E 上升;组 T 中的葡萄糖依赖性胰岛素释放肽(GIP)反应增加。组 T 中的胰岛素敏感性增加,但组 E 中未改变。
在健康的年轻男性中,性激素的短期变化会影响餐后甘油三酯和 GIP 反应以及胰岛素敏感性。