Department of Physical Therapy and Athletic Training, University of Utah, 520 Wakara Way, Salt Lake City, UT 84018, USA.
Department of Nutrition and Integrative Physiology, University of Utah, 250 S. 1850 E, Room 214, Salt Lake City, UT 84112, USA.
Appl Physiol Nutr Metab. 2020 Nov;45(11):1261-1269. doi: 10.1139/apnm-2020-0064. Epub 2020 May 29.
With this cohort, we previously demonstrated preservation of thigh lean tissue with neuromuscular electrical stimulation combined with protein supplementation (NMES+PRO) treatment during bed rest in healthy older adults. Because macrophage polarization plays a significant role in the repair and maintenance of muscle size and insulin sensitivity, we hypothesized that muscle macrophages would be induced by NMES+PRO and would correspond to an increase in lean mass and an attenuated insulin resistance response altered by bed rest. Older adults (60-80 years old; body mass index < 30 kg/m) underwent 5 days of bed rest and were randomized to either thrice daily treatment of NMES+PRO ( = 8) or CON ( = 8). Lean mass, insulin sensitivity, and markers of muscle macrophages, inflammation, and connective tissue were determined before and after bed rest. Glucose intolerance and insulin resistance occurred after bed rest but there was not a treatment effect ( > 0.10). Proinflammatory-like macrophages (CD11b, CD206) increased ( < 0.05) with NMES+PRO treatment and was different than CON. Minor changes in noncontractile tissue were observed. However, changes in muscle macrophages or extracellular matrix were not related to the preservation of thigh lean mass or insulin resistance. Daily NMES+PRO treatment during bed rest induced a muscle proinflammatory-like macrophage response and was unrelated to muscle size or metabolic function. This study is listed as clinical trial NCT02566590. Neuromuscular electrical stimulation combined with protein supplementation (NMES+PRO) increased proinflammatory-like macrophages and extracellular matrix content in older adults after bed rest. NMES+PRO changes in macrophages and noncontractile tissue macrophages were not related to muscle size preservation or insulin sensitivity.
在这项队列研究中,我们之前曾表明,在健康老年人卧床休息期间,神经肌肉电刺激联合蛋白质补充(NMES+PRO)治疗可保留大腿瘦组织。因为巨噬细胞极化在肌肉大小和胰岛素敏感性的修复和维持中起着重要作用,所以我们假设 NMES+PRO 会诱导肌肉巨噬细胞,并与瘦体重增加和卧床休息引起的胰岛素抵抗反应减弱相对应。老年人(60-80 岁;体重指数<30kg/m)接受 5 天卧床休息,并随机分为每日三次 NMES+PRO 治疗组(n=8)或对照组(n=8)。在卧床休息前后测定瘦体重、胰岛素敏感性以及肌肉巨噬细胞、炎症和结缔组织的标志物。卧床休息后出现葡萄糖不耐受和胰岛素抵抗,但无治疗作用(>0.10)。NMES+PRO 治疗后,促炎样巨噬细胞(CD11b、CD206)增加(<0.05),与对照组不同。非收缩组织的变化较小。然而,肌肉巨噬细胞或细胞外基质的变化与大腿瘦体重或胰岛素抵抗的保留无关。卧床休息期间每日 NMES+PRO 治疗可诱导肌肉促炎样巨噬细胞反应,与肌肉大小或代谢功能无关。这项研究已在临床试验 NCT02566590 中注册。神经肌肉电刺激联合蛋白质补充(NMES+PRO)可增加卧床休息后老年人的促炎样巨噬细胞和细胞外基质含量。巨噬细胞和非收缩组织巨噬细胞的 NMES+PRO 变化与肌肉大小的保留或胰岛素敏感性无关。