STAT5 activation and cardioprotection by remote ischemic preconditioning in humans: short communication

STAT5 激活和人类远程缺血预处理的心脏保护:简短交流

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作者:Gerd Heusch, Judith Musiolik, Eva Kottenberg, Jürgen Peters, Heinz Jakob, Matthias Thielmann

Conclusions

The identification of this unique signaling signature of RIPC will facilitate the development of pharmacological cardioprotection. Clinical

Objective

To identify cardioprotective signaling by RIPC in humans.

Results

RIPC was induced by 3 cycles of 5 minutes of arm ischemia/5 minutes of reperfusion in patients undergoing coronary artery bypass surgery. Twelve patients each were randomly assigned to undergo RIPC or a sham control procedure. Protection was confirmed by reduced serum troponin I concentrations in patients with RIPC versus control patients. In myocardial biopsies, an array of established cardioprotective proteins was analyzed by Western immunoblotting. The phosphorylation of signal transducer and activator of transcription 5 (STAT5) increased from baseline before ischemic cardioplegic arrest to 10 minutes of reperfusion with RIPC, and STAT5 phosphorylation during reperfusion was greater in patients with RIPC than in control patients. Conclusions: The identification of this unique signaling signature of RIPC will facilitate the development of pharmacological cardioprotection. Clinical

Trial registration

URL: http://www.clinicaltrials.gov. Unique identifier: NCT01406678.

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