Departments of Physical Therapy and Athletic Training, University of Utah, Salt Lake City, Utah.
University of Utah School of Medicine, Salt Lake City, Utah.
Acta Physiol (Oxf). 2019 Jun;226(2):e13251. doi: 10.1111/apha.13251. Epub 2019 Jan 30.
Mechanisms underlying physical inactivity-induced insulin resistance are not well understood. In addition to a role in muscle repair, immune cell populations such as macrophages may regulate insulin sensitivity.
The aim of this study was to examine if the dynamic changes in insulin sensitivity during and after recovery from reduced physical activity corresponded to changes in skeletal muscle macrophages.
In this prospective clinical study, we collected muscle biopsies from healthy older adults (70 ± 2 years, n = 12) before and during a hyperinsulinaemic-euglycaemic clamp and this occurred before (PRE) and after 2-week reduced physical activity (RA), and following 2-week of recovery (REC). Insulin sensitivity (hyperinsulinaemic-euglycaemic clamp), skeletal muscle mRNA expression of inflammatory markers, and immunofluorescent quantification of skeletal muscle macrophages, myofibre-specific satellite cell and capillary content were assessed.
Insulin sensitivity was decreased following reduced activity and rebounded following recovery above PRE levels. We observed an increase (P < 0.01) in muscle macrophages (CD68 CD206 : 190 [55, 324]; CD11b CD206 : 117 [28, 205]% change from PRE) and CD68 (2.4 [1.4, 3.4]-fold) and CCL2 (1.9 [1.3, 2.5]-fold) mRNA following RA concurrent with increased (P < 0.03) satellite cells (55 [6, 104]%) in slow-twitch myofibres. Moreover, the distance of satellite cells to the nearest capillary was increased 7.7 (1.7, 13.7) µm in fast-twitch myofibres at RA (P = 0.007). Changes in macrophages were positively associated with increased insulin sensitivity following RA (R > 0.57, P < 0.05).
These findings suggested that a dynamic response of skeletal muscle macrophages following acute changes in physical activity in healthy older adults is related to insulin sensitivity.
体力活动减少导致胰岛素抵抗的机制尚不清楚。除了在肌肉修复中的作用外,免疫细胞群体(如巨噬细胞)也可能调节胰岛素敏感性。
本研究旨在探讨在减少体力活动期间和之后,胰岛素敏感性的动态变化是否与骨骼肌巨噬细胞的变化相对应。
在这项前瞻性临床研究中,我们在健康老年人(70±2 岁,n=12)进行高胰岛素-正常血糖钳夹之前和期间采集肌肉活检,这发生在减少体力活动之前(PRE)和之后 2 周(RA),以及之后 2 周的恢复期(REC)。评估了胰岛素敏感性(高胰岛素-正常血糖钳夹)、骨骼肌炎症标志物的 mRNA 表达以及骨骼肌巨噬细胞、肌纤维特异性卫星细胞和毛细血管含量的免疫荧光定量。
体力活动减少后胰岛素敏感性降低,恢复后恢复至高于 PRE 水平。我们观察到肌肉巨噬细胞(CD68 CD206:190[55,324];CD11b CD206:117[28,205]%从 PRE 开始变化)和 CD68(2.4[1.4,3.4] -倍)和 CCL2(1.9[1.3,2.5] -倍)mRNA 增加(P<0.01),同时慢肌纤维中的卫星细胞(55[6,104]%)增加。此外,RA 时快肌纤维中卫星细胞到最近毛细血管的距离增加了 7.7(1.7,13.7)µm(P=0.007)。RA 后,巨噬细胞的变化与胰岛素敏感性的增加呈正相关(R>0.57,P<0.05)。
这些发现表明,健康老年人急性体力活动变化后骨骼肌巨噬细胞的动态反应与胰岛素敏感性有关。