changes of myogenic reactive oxygen species and interleukin-6 in contracting skeletal muscle cells肌原性的活性氧物种的变化在承包骨骼肌细胞和白细胞介素- 6.pdfVIP
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changes of myogenic reactive oxygen species and interleukin-6 in contracting skeletal muscle cells肌原性的活性氧物种的变化在承包骨骼肌细胞和白细胞介素- 6
Hindawi Publishing Corporation
Oxidative Medicine and Cellular Longevity
Volume 2012, Article ID 145418, 6 pages
doi:10.1155/2012/145418
Research Article
Changes of Myogenic Reactive Oxygen Species and
Interleukin-6 in Contracting Skeletal Muscle Cells
Hongying Pan,1 Xiaoyang Xu,1 Xuanming Hao,1 and Yajun Chen2
1 College of Sports Science, South China Normal University, Guangzhou 510006, China
2 Department of Maternity and Child Health Care, School of Public Health, Sun Yat-Sen University, Guangzhou 510080, China
Correspondence should be addressed to Yajun Chen, chenyj68@
Received 13 January 2012; Revised 28 February 2012; Accepted 29 February 2012
Academic Editor: Michalis G. Nikolaidis
Copyright © 2012 Hongying Pan et al. This is an open access article distributed under the Creative Commons Attribution License,
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The aim of this study was to measure changes in myotube reactive oxygen species (ROS) and the production of interleukin (IL)-6 in
electrically stimulated mouse C2C12 skeletal muscle cells. After five days of differentiation, myotubes were stimulated using an elec-
trical stimulator set at 45 V at a frequency of 5 Hz, with a pulse width of 20 ms. Acute stimulations were performed for 45, 60, 75,
90, or 120 min in each dish. ROSs were detected in the extracted cells directly using a fluorescent probe. IL-6 mRNA expression in
C2C12 myotubes and IL-6 concentration in C2C12 myotube supernatants were determined using real-time PCR and ELISA, res-
pectively. Compared with control cells, ROS generation was significantly increased at 45 min after the onset of stimulation (P
0.01) and continued to increase, reaching a maximum at 120 min. IL-6 mRNA expression and I
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