Department of Medicine, Knight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon.
Division of Endocrinology, Diabetes, Clinical Nutrition, Oregon Health & Science University, Portland, Oregon.
Endocrinology. 2019 Apr 1;160(4):899-914. doi: 10.1210/en.2018-00884.
Whether hormone replacement therapy has beneficial metabolic effects in postmenopausal women remains controversial because of between-study differences in menopausal duration, estrogen formulations, and diet. Additionally, animal studies have not reflected the typical human obesogenic, Western-style diet (WSD). In this study, we determined the effects of immediate 17β-estradiol (ImE) or delayed 17β-estradiol treatment on weight and metabolism parameters in old ovo-hysterectomized rhesus macaques consuming a WSD over a 30-month period. The placebo and ImE groups exhibited progressive gains in weight and fat mass, which ImE initially attenuated but did not prevent. Progression of insulin resistance (IR) was lessened by ImE compared with placebo under both fasting and IV glucose-stimulated conditions, plateauing in all groups between 24 and 30 months. Consequently, relative euglycemia was maintained through lower stimulated insulin levels with ImE than with placebo. Bone mineral density decreased in the placebo group but was maintained in the ImE group, whereas bone mineral content was unaffected by placebo and increased with ImE. Daily activity was reduced while macaques consumed a WSD and was not affected by ImE. Over time, total cholesterol, triglyceride, very-low-density cholesterol, high-density lipoprotein cholesterol (HDL-C), non-HDL-C, and IL-8 levels increased or trended upward in all animals, with only the change in HDL-C affected by ImE. Delayed estrogen treatment (months 24 to 30) had no significant impact on body composition or glucometabolic parameters. In summary, detrimental WSD-induced changes in body composition and metabolism were only temporarily ameliorated by ImE, with the important exception of glucose homeostasis, which benefited from E replacement even as body composition worsened.
激素替代疗法是否对绝经后妇女具有有益的代谢作用仍存在争议,这是因为研究之间的绝经持续时间、雌激素制剂和饮食存在差异。此外,动物研究并未反映出典型的人类致肥胖的西方饮食(WSD)。在这项研究中,我们确定了立即给予 17β-雌二醇(ImE)或延迟给予 17β-雌二醇治疗对 30 个月内食用 WSD 的老卵-子宫切除恒河猴体重和代谢参数的影响。与安慰剂组相比,ImE 组的体重和脂肪量逐渐增加,ImE 最初减轻了这种增加,但并未阻止。与安慰剂相比,ImE 可减轻胰岛素抵抗(IR)的进展,无论是在空腹还是静脉内葡萄糖刺激条件下,所有组在 24 至 30 个月之间达到平台期。因此,与安慰剂相比,ImE 组通过较低的刺激胰岛素水平维持相对的血糖正常。安慰剂组的骨密度下降,但 ImE 组保持不变,而安慰剂对骨矿物质含量没有影响,ImE 组则增加。当恒河猴食用 WSD 时,其日常活动减少,而 ImE 对其没有影响。随着时间的推移,所有动物的总胆固醇、甘油三酯、极低密度胆固醇、高密度脂蛋白胆固醇(HDL-C)、非高密度脂蛋白胆固醇和白细胞介素-8 水平升高或呈上升趋势,只有 HDL-C 的变化受 ImE 影响。延迟的雌激素治疗(第 24 至 30 个月)对身体成分或糖代谢参数没有显著影响。总之,ImE 仅暂时改善了 WSD 引起的身体成分和代谢的有害变化,只有葡萄糖稳态是一个重要的例外,即使身体成分恶化,E 替代仍有益于葡萄糖稳态。