4.4 Article

Gene transcripts expressed in equine white blood cells are potential biomarkers of extracorporeal shock wave therapy

Journal

DRUG TESTING AND ANALYSIS
Volume 14, Issue 5, Pages 973-982

Publisher

WILEY
DOI: 10.1002/dta.3099

Keywords

horse; inflammatory cytokine; lithotripsy; microarray; transcriptome

Funding

  1. Pennsylvania Department of Agriculture State Horse Racing Commission
  2. Pennsylvania Harness Horseman's Association
  3. Meadows Standardbred Owners Association
  4. Pennsylvania Horsemen's Benevolent and Protective Association
  5. Racing Medication and Testing Consortium

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Extracorporeal shockwave therapy (ESWT) is a treatment for musculoskeletal injuries in equine athletes, and changes in white blood cell gene transcripts may serve as biomarkers for assessing its effects.
Extracorporeal shockwave therapy (ESWT) is a treatment applied to musculoskeletal injuries in equine athletes to alleviate pain and accelerate healing. ESWT also causes acute tissue damage. Therefore, its ability to act as an analgesic and cause tissue damage potentially increases the risk of a catastrophic event if used shortly before a strenuous competition such as horseracing. While ESWT is prohibited by many racing jurisdictions within 10 days prior to competition, a test to detect whether a horse has received ESWT is needed. ESWT changes the protein levels of inflammatory mediators in blood, and white blood cells (WBC) typically produce these proteins. Changes in gene expression precede changes in protein production; thus, it was hypothesized that WBC gene transcripts might serve as biomarkers of ESWT. To test this hypothesis, six thoroughbred horses received a single administration of ESWT to the distal limb, and WBC RNA was extracted from blood samples collected before (0 h) and after ESWT (2, 4, 6, 24, 48, and 72 h). Targeted and untargeted analyses evaluated the transcriptome using quantitative PCR (qPCR) and microarray. The expression of IL-1 alpha, IL-1 beta, TNF-alpha, IL-1Ra1, IL-1Ra2 and TGF-beta 1, and BMPR1A in circulating WBCs was significantly up-regulated, while IFN-gamma, ZNF483, TMEM80, CAH6, ENPP, and S8723 were significantly down-regulated at various time points following ESWT. These data support the hypothesis that changes in WBC gene transcripts could serve as biomarkers for ESWT.

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