Effects of corticosteroid on the expressions of neuropeptide and cytokine mRNA and on tenocyte viability in lateral epicondylitis

被引:25
|
作者
Han, Soo Hong [1 ]
An, Hee Jung [2 ]
Song, Ji Ye [3 ]
Shin, Dong Eun [1 ]
Do Kwon, Young [4 ]
Shim, Jong Sup [5 ]
Lee, Soon Chul [1 ]
机构
[1] CHA Univ, CHA Bundang Med Ctr, Dept Orthopaed Surg, Gyeonggi Do 463712, South Korea
[2] CHA Univ, CHA Bundang Med Ctr, Dept Pathol, Gyeonggi Do 463712, South Korea
[3] CHA Univ, CHA Bundang Med Ctr, Inst Clin Res, Gyeonggi Do 463712, South Korea
[4] CHA Univ, Grad Sch, Dept Biomed Sci, Gyeonggi Do 463712, South Korea
[5] Sungkyunkwan Univ, Samsung Med Ctr, Dept Orthopaed Surg, Seoul 135710, South Korea
来源
JOURNAL OF INFLAMMATION-LONDON | 2012年 / 9卷
关键词
Lateral epicondylitis; Corticosteroid; Neuropeptide; mRNA; Tenocyte viability; BREVIS MUSCLE ORIGIN; SUBSTANCE-P; SENSORY NEUROPEPTIDES; TENNIS ELBOW; TGF-BETA; TENDON; GLUCOCORTICOIDS; CELLS; TENDINOPATHY; MODULATION;
D O I
10.1186/1476-9255-9-40
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: The purpose of this study was to determine the reaction mechanism of corticosteroid by analyzing the expression patterns of neuropeptides (substance P (SP), calcitonin gene related peptide (CGRP)) and of cytokines (interleukin (IL)-1 alpha, tumor growth factor (TGF)-beta) after corticosteroid treatment in lateral epicondylitis. In addition, we also investigated whether corticosteroid influenced tenocyte viability. Methods: The corticosteroid triamcinolone acetonide (TAA) was applied to cultured tenocytes of lateral epicondylitis, and the changes in the mRNA expressions of neuropeptides and cytokines and tenocyte viabilities were analyzed at seven time points. Quantitative real-time polymerase chain reaction and an MTT assay were used. Results: The expression of SP mRNA was maximally inhibited by TAA at 24 hours but recovered at 72 hours, and the expressions of CGRP mRNA and IL 1 alpha mRNA were inhibited at 24 and 3 hours, respectively. The expression of TGF-beta mRNA was not significant. Tenocyte viability was significantly reduced by TAA at 24 hours. Conclusions: We postulate that the reaction mechanism predominantly responsible for symptomatic relief after a corticosteroid injection involves the inhibitions of neuropeptides and cytokines, such as, CGRP and IL-1 alpha. However the tenocyte viability was compromised by a corticosteroid.
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页数:9
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