Gibb Fraser W, Homer Natalie Z M, Faqehi Abdullah M M, Upreti Rita, Livingstone Dawn E, McInnes Kerry J, Andrew Ruth, Walker Brian R
British Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Queen's Medical Research Institute, Edinburgh EH16 4TJ, United Kingdom.
J Clin Endocrinol Metab. 2016 May;101(5):2040-6. doi: 10.1210/jc.2015-4146. Epub 2016 Mar 11.
Deficiency of aromatase, the enzyme that catalyzes the conversion of androgens to estrogens, is associated with insulin resistance in humans and mice.
We hypothesized that pharmacological aromatase inhibition results in peripheral insulin resistance in humans.
This was a double-blind, randomized, controlled, crossover study.
The study was conducted at a clinical research facility.
Seventeen healthy male volunteers (18-50 y) participated in the study.
The intervention included oral anastrozole (1 mg daily) and placebo, each for 6 weeks with a 2-week washout period.
Glucose disposal and rates of lipolysis were measured during a stepwise hyperinsulinemic euglycemic clamp. Data are mean (SEM).
Anastrozole therapy resulted in significant estradiol suppression (59.9 ± 3.6 vs 102.0 ± 5.7 pmol/L, P = < .001) and a more modest elevation of total T (25.8 ± 1.2 vs 21.4 ± 0.7 nmol/L, P = .003). Glucose infusion rate, during the low-dose insulin infusion, was lower after anastrozole administration (12.16 ± 1.33 vs 14.15 ± 1.55 μmol/kg·min, P = .024). No differences in hepatic glucose production or rate of lipolysis were observed.
Aromatase inhibition reduces insulin sensitivity, with respect to peripheral glucose disposal, in healthy men. Local generation and action of estradiol, at the level of skeletal muscle, is likely to be an important determinant of insulin sensitivity.
芳香化酶是一种催化雄激素转化为雌激素的酶,其缺乏与人类和小鼠的胰岛素抵抗有关。
我们假设药物性芳香化酶抑制会导致人类外周胰岛素抵抗。
这是一项双盲、随机、对照、交叉研究。
该研究在临床研究机构进行。
17名健康男性志愿者(18 - 50岁)参与了该研究。
干预包括口服阿那曲唑(每日1毫克)和安慰剂,各为期6周,中间有2周的洗脱期。
在逐步高胰岛素正常血糖钳夹期间测量葡萄糖处置和脂肪分解率。数据为平均值(标准误)。
阿那曲唑治疗导致雌二醇显著降低(59.9 ± 3.6对102.0 ± 5.7皮摩尔/升,P = <.001),总睾酮有更适度的升高(25.8 ± 1.2对21.4 ± 0.7纳摩尔/升,P =.003)。在低剂量胰岛素输注期间,阿那曲唑给药后葡萄糖输注率较低(12.16 ± 1.33对14.15 ± 1.55微摩尔/千克·分钟,P =.024)。未观察到肝葡萄糖生成或脂肪分解率的差异。
在健康男性中,芳香化酶抑制会降低外周葡萄糖处置方面的胰岛素敏感性。骨骼肌水平的雌二醇局部生成和作用可能是胰岛素敏感性的重要决定因素。