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卧床休息期间毛细血管稀疏的程度小于纤维萎缩和氧化能力丧失的程度。

Capillary rarefaction during bed rest is proportionally less than fibre atrophy and loss of oxidative capacity.

机构信息

Research Centre for Musculoskeletal Science & Sports Medicine, Department of Life Sciences, Manchester Metropolitan University, Manchester, UK.

School of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds, UK.

出版信息

J Cachexia Sarcopenia Muscle. 2022 Dec;13(6):2712-2723. doi: 10.1002/jcsm.13072. Epub 2022 Sep 13.

Abstract

BACKGROUND

Muscle disuse from bed rest or spaceflight results in losses in muscle mass, strength and oxidative capacity. Capillary rarefaction may contribute to muscle atrophy and the reduction in oxidative capacity during bed rest. Artificial gravity may attenuate the negative effects of long-term space missions or bed rest. The aim of the present study was to assess (1) the effects of bed rest on muscle fibre size, fibre type composition, capillarization and oxidative capacity in the vastus lateralis and soleus muscles after 6 and 55 days of bed rest and (2) the effectiveness of artificial gravity in mitigating bed-rest-induced detriments to these parameters.

METHODS

Nineteen participants were assigned to a control group (control, n = 6) or an intervention group undergoing 30 min of centrifugation (n = 13). All underwent 55 days of head-down tilt bed rest. Vastus lateralis and soleus biopsies were taken at baseline and after 6 and 55 days of bed rest. Fibre type composition, fibre cross-sectional area, capillarization indices and oxidative capacity were determined.

RESULTS

After just 6 days of bed rest, fibre atrophy (-23.2 ± 12.4%, P < 0.001) and reductions in capillary-to-fibre ratio (C:F; 1.97 ± 0.57 vs. 1.56 ± 0.41, P < 0.001) were proportional in both muscles as reflected by a maintained capillary density. Fibre atrophy proceeded at a much slower rate between 6 and 55 days of bed rest (-11.6 ± 12.1% of 6 days, P = 0.032) and was accompanied by a 19.1% reduction in succinate dehydrogenase stain optical density (P < 0.001), without any further significant decrements in C:F (1.56 ± 0.41 vs. 1.49 ± 0.37, P = 0.459). Consequently, after 55 days of bed rest, the capillary supply-oxidative capacity ratio of a fibre had increased by 41.9% (P < 0.001), indicating a capillarization in relative excess of oxidative capacity. Even though the heterogeneity of capillary spacing (Log SD) was increased after 55 days by 12.7% (P = 0.004), tissue oxygenation at maximal oxygen consumption of the fibres was improved after 55 days bed rest. Daily centrifugation failed to blunt the bed-rest-induced reductions in fibre size and oxidative capacity and capillary rarefaction.

CONCLUSIONS

The relationship between fibre size and oxidative capacity with the capillary supply of a fibre is uncoupled during prolonged bed rest as reflected by a rapid loss of muscle mass and capillaries, followed at later stages by a more than proportional loss of mitochondria without further capillary loss. The resulting excessive capillary supply of the muscle after prolonged bed rest is advantageous for the delivery of substrates needed for subsequent muscle recovery.

摘要

背景

卧床或太空飞行导致的肌肉废用会导致肌肉质量、力量和氧化能力下降。毛细血管稀疏可能导致肌肉萎缩和卧床休息期间氧化能力的降低。人工重力可能会减轻长期太空任务或卧床休息的负面影响。本研究的目的是评估(1)卧床休息 6 天和 55 天后对股外侧肌和比目鱼肌的肌纤维大小、纤维类型组成、毛细血管化和氧化能力的影响,以及(2)人工重力对减轻卧床休息对这些参数的不利影响的有效性。

方法

19 名参与者被分配到对照组(对照组,n=6)或接受 30 分钟离心的干预组(n=13)。所有参与者均接受 55 天的头低位倾斜卧床休息。在基线和卧床休息 6 天和 55 天后采集股外侧肌和比目鱼肌活检。测定纤维类型组成、纤维横截面积、毛细血管化指数和氧化能力。

结果

仅仅卧床休息 6 天后,股外侧肌和比目鱼肌的纤维萎缩(分别为-23.2±12.4%,P<0.001)和毛细血管与纤维比(C:F;1.97±0.57 与 1.56±0.41,P<0.001)的减少呈比例,这反映了毛细血管密度的维持。在卧床休息 6 天至 55 天期间,纤维萎缩的速度要慢得多(6 天的-11.6±12.1%,P=0.032),同时伴随着琥珀酸脱氢酶染色光密度降低 19.1%(P<0.001),而 C:F 没有进一步显著降低(1.56±0.41 与 1.49±0.37,P=0.459)。因此,卧床休息 55 天后,纤维的毛细血管供应-氧化能力比增加了 41.9%(P<0.001),表明毛细血管化相对于氧化能力的增加。尽管卧床休息 55 天后毛细血管间隔的异质性(Log SD)增加了 12.7%(P=0.004),但在卧床休息 55 天后,纤维最大摄氧量时的组织氧合得到改善。每日离心并不能阻止卧床休息引起的纤维大小和氧化能力以及毛细血管稀疏的减少。

结论

在长时间卧床休息期间,纤维大小和氧化能力与纤维毛细血管供应之间的关系失去了耦合,这反映在肌肉质量和毛细血管迅速丧失之后,随后是线粒体的不成比例丧失,而没有进一步的毛细血管丧失。长时间卧床休息后肌肉中过多的毛细血管供应有利于输送随后肌肉恢复所需的底物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7e6/9745458/2a283e3eba74/JCSM-13-2712-g004.jpg

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