Evidence map›Paper›PMID 31464636›Full record

ArticleSkeletal muscle2019

Ibuprofen inhibited migration of skeletal muscle cells in association with downregulation of p130cas and CrkII expressions.

Chih-Hao Liao, Li-Ping Lin, Tung-Yang Yu, Chih-Chin Hsu, Jong-Hwei S Pang, Wen-Chung Tsai

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Article in Skeletal muscle, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Chih-Hao LiaoDepartment of Physical Medicine and Rehabilitation, Chang Gung Memorial Hospital, No.123, Dinghu Rd., Guishan Dist, Taoyuan City, 333, Taiwan.
Li-Ping LinDepartment of Physical Medicine and Rehabilitation, Chang Gung Memorial Hospital, No.123, Dinghu Rd., Guishan Dist, Taoyuan City, 333, Taiwan.
Tung-Yang YuDepartment of Physical Medicine and Rehabilitation, Chang Gung Memorial Hospital, No.123, Dinghu Rd., Guishan Dist, Taoyuan City, 333, Taiwan.
Chih-Chin HsuCollege of Medicine, Chang Gung University, Taoyuan City, Taiwan.
Jong-Hwei S PangDepartment of Physical Medicine and Rehabilitation, Chang Gung Memorial Hospital, No.123, Dinghu Rd., Guishan Dist, Taoyuan City, 333, Taiwan.
Wen-Chung TsaiDepartment of Physical Medicine and Rehabilitation, Chang Gung Memorial Hospital, No.123, Dinghu Rd., Guishan Dist, Taoyuan City, 333, Taiwan. tsaiwc@cgmh.org.tw.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNonsteroidal anti-inflammatory drugs (NSAIDs) are commonly used to treat sports-related muscle injuries. However, NSAIDs were recently shown to impede the muscle healing process after acute injury. Migration of skeletal muscle cells is a crucial step during the muscle healing process. The present study was performed to investigate the effect and molecular mechanisms of action of ibuprofen, a commonly used NSAID, on the migration of skeletal muscle cells.

methodsSkeletal muscle cells isolated from the gastrocnemius muscle of Sprague-Dawley rats were treated with ibuprofen. MTT assay (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) was used to evaluate cell viability, and cell apoptosis was evaluated by TUNEL assay, after ibuprofen treatment. Skeletal muscle cell migration and spreading were evaluated using the transwell filter migration assay and F-actin staining, respectively. The protein expression of p130cas and CrkII, which are cell migration facilitating genes, was determined by western blot analysis. The overexpression of p130cas of muscle cells was achieved by p130cas vector transfection.

resultsThe results demonstrated that ibuprofen did not have a significant negative effect on cell viability and apoptosis. Ibuprofen inhibited the migration and spreading of skeletal muscle cells in a dose-dependent manner. Ibuprofen also dose-dependently decreased the protein expression of p130cas and CrkII. Furthermore, overexpression of p130cas resulted in the promotion of cell migration and spreading and counteracted ibuprofen-mediated inhibition.

conclusionThis study suggested that ibuprofen exerts a potentially adverse effect on the migration of skeletal muscle cells by downregulating protein expression of p130cas and CrkII. These results indicate a possible mechanism underlying the possible negative effect of NSAIDs on muscle regeneration.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalAthletic InjuriesCell MovementCells, CulturedCrk-Associated Substrate ProteinDown-RegulationHumansIbuprofenMuscle Fibers, SkeletalMuscle, SkeletalProto-Oncogene Proteins c-crkRatsRats, Sprague-DawleyRegenerationWound HealingAnti-Inflammatory Agents, Non-SteroidalBcar1 protein, ratCrk-Associated Substrate ProteinIbuprofenProto-Oncogene Proteins c-crkCell migrationIbuprofenSkeletal muscleSport injury

Identifiers

PMID31464636
PMCPMC6714350

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.