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抗阻运动后恢复方式下单核细胞迁移的介质

Mediators of monocyte migration in response to recovery modalities following resistance exercise.

作者信息

Jajtner Adam R, Fragala Maren S, Townsend Jeremy R, Gonzalez Adam M, Wells Adam J, Fukuda David H, Stout Jeffrey R, Hoffman Jay R

机构信息

Institute of Exercise Physiology and Wellness, University of Central Florida, Orlando, FL, USA.

出版信息

Mediators Inflamm. 2014;2014:145817. doi: 10.1155/2014/145817. Epub 2014 Jun 2.

Abstract

Mediators of monocyte migration, complement receptor-3 (CR3), and chemokine ligand-4 (CCL4) were measured in response to recovery modalities following resistance exercise. Thirty resistance-trained men (23.1 ± 2.9 y; 175.2 ± 7.1 cm; 82.1 ± 8.4 kg) were given neuromuscular electric stimulation (NMES), cold water immersion (CWI), or control (CON) treatments immediately following resistance exercise. Blood samples were obtained preexercise (PRE), immediately (IP), 30 minutes (30 P), 24 hours (24 H), and 48 hours (48 H) after exercise for measurement of circulating CCL4 and CR3 expression on CD14+ monocytes, by assay and flow cytometry. Circulating CCL4 showed no consistent changes. Inferential analysis indicated that CR3 expression was likely greater in CON at 30 P than NMES (90.0%) or CWI (86.8%). NMES was likely lower than CON at 24 H (92.9%) and very likely lower at 48 H (98.7%). Expression of CR3 following CWI was very likely greater than CON (96.5%) at 24 H. The proportion of CR3+ monocytes was likely greater following CWI than NMES (85.8%) or CON (85.2%) at 24 H. The change in proportion of CR3+ monocytes was likely (86.4%) greater following NMES than CON from IP to 30 P. The increased expression of CR3 and increased proportion of CR3+ monocytes following CWI at 24 H indicate a potentially improved ability for monocyte adhesion to the endothelium, possibly improving phagocytosis of damaged tissues.

摘要

在抗阻运动后的恢复方式下,对单核细胞迁移介质、补体受体-3(CR3)和趋化因子配体-4(CCL4)进行了测量。30名进行抗阻训练的男性(23.1±2.9岁;175.2±7.1厘米;82.1±8.4千克)在抗阻运动后立即接受神经肌肉电刺激(NMES)、冷水浸泡(CWI)或对照(CON)处理。在运动前(PRE)、运动后即刻(IP)、30分钟(30P)、24小时(24H)和48小时(48H)采集血样,通过检测和流式细胞术测量循环中CCL4以及CD14+单核细胞上CR3的表达。循环中的CCL4未显示出一致的变化。推断分析表明,在30P时,CON组的CR3表达可能高于NMES组(90.0%)或CWI组(86.8%)。在24H时,NMES组的CR3表达可能低于CON组(92.9%),在48H时很可能更低(98.7%)。在24H时,CWI组的CR3表达很可能高于CON组(96.5%)。在24H时,CWI组CR3+单核细胞的比例很可能高于NMES组(85.8%)或CON组(85.2%)。从IP到30P,NMES组CR3+单核细胞比例的变化很可能(86.4%)大于CON组。在24H时,CWI组CR3表达增加以及CR3+单核细胞比例增加表明单核细胞与内皮细胞黏附的能力可能得到改善,这可能会增强对受损组织的吞噬作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59cf/4060064/740dbe54f44d/MI2014-145817.001.jpg

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