Departments of Pediatrics and Medicine, Columbia University College of Physicians and Surgeons, New York, New York.
Division of Cardiology, Department of Medicine, Columbia University College of Physicians and Surgeons , New York, New York.
Am J Physiol Endocrinol Metab. 2018 Nov 1;315(5):E771-E779. doi: 10.1152/ajpendo.00116.2018. Epub 2018 Jun 19.
Subjects maintaining a ≥10% dietary weight loss exhibit decreased circulating concentrations of bioactive thyroid hormones and increased skeletal muscle work efficiency largely due to increased expression of more-efficient myosin heavy chain (MHC) isoforms (MHC I) and significantly mediated by the adipocyte-derived hormone leptin. The primary purpose of this study was to examine the effects of triiodothyronine (T) repletion on energy homeostasis and skeletal muscle physiology in weight-reduced subjects and to compare these results with the effects of leptin repletion. Nine healthy in-patients with obesity were studied at usual weight (Wt) and following a 10% dietary weight loss while receiving 5 wk of a placebo (Wt) or T (Wt) in a single-blind crossover design. Primary outcome variables were skeletal muscle work efficiency and vastus lateralis muscle mRNA expression. These results were compared with the effects of leptin repletion in a population of 22 subjects, some of whom participated in a previous study. At Wt, skeletal muscle work efficiency and relative expression of the more-efficient/less-efficient MHC I/MHC II isoforms were significantly increased and the ratio of the less-efficient to the more-efficient sarco(endo)plasmic reticulum Ca-ATPase isoforms (SERCA1/SERCA2) was significantly decreased. These changes were largely reversed by T repletion to a degree similar to the changes that occurred with leptin repletion. These data support the hypothesis that the effects of leptin on energy expenditure in weight-reduced individuals are largely mediated by T and suggest that further study of the possible role of thyroid hormone repletion as adjunctive therapy to help sustain weight loss is needed.
受试者保持 ≥10%的饮食减重会导致循环生物活性甲状腺激素浓度降低,骨骼肌工作效率增加,主要是由于更有效的肌球蛋白重链 (MHC) 同工型 (MHC I) 的表达增加,而这主要是由脂肪细胞衍生的激素瘦素介导的。本研究的主要目的是检查三碘甲状腺原氨酸 (T) 补充对减重受试者能量平衡和骨骼肌生理学的影响,并将这些结果与瘦素补充的影响进行比较。在一项单盲交叉设计中,9 名肥胖住院患者在通常体重 (Wt) 和接受 5 周安慰剂 (Wt) 或 T (Wt) 治疗后,进行了 10%饮食减重研究。主要观察变量是骨骼肌工作效率和股外侧肌 mRNA 表达。这些结果与 22 名受试者的瘦素补充效果进行了比较,其中一些受试者参加了之前的研究。在 Wt 时,骨骼肌工作效率和更有效的/效率较低的 MHC I/MHC II 同工型的相对表达显著增加,效率较低的肌浆内质网 Ca-ATPase 同工型 (SERCA1/SERCA2) 与更有效的同工型的比值显著降低。这些变化在很大程度上被 T 补充所逆转,程度与瘦素补充所引起的变化相似。这些数据支持瘦素对减重个体能量消耗的影响主要是通过 T 介导的假设,并表明需要进一步研究甲状腺激素补充作为辅助治疗以帮助维持体重减轻的可能作用。