A 2 × 2 factorial design for the combination therapy of minocycline and remote ischemic perconditioning: efficacy in a preclinical trial in murine thromboembolic stroke model

After the failure of so many drugs and therapies for acute ischemic stroke, innovative approaches are needed to develop new treatments. One promising strategy is to test combinations of agents in the pre-hospital setting prior to the administration of intravenous tissue plasminogen activator (IV-tPA...

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Veröffentlicht in:Experimental & translational stroke medicine 2014-10, Vol.6 (1), p.10-10, Article 10
Hauptverfasser: Hoda, Md Nasrul, Fagan, Susan C, Khan, Mohammad B, Vaibhav, Kumar, Chaudhary, Aizaz, Wang, Phillip, Dhandapani, Krishnan M, Waller, Jennifer L, Hess, David C
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Sprache:eng
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Zusammenfassung:After the failure of so many drugs and therapies for acute ischemic stroke, innovative approaches are needed to develop new treatments. One promising strategy is to test combinations of agents in the pre-hospital setting prior to the administration of intravenous tissue plasminogen activator (IV-tPA) and/ or the use of mechanical reperfusion devices in the hospital. We performed a 2 × 2 factorial design preclinical trial where we tested minocycline (MINO), remote ischemic perconditioning (RIPerC) and their combination treatment in a thromboembolic clot model of stroke in mice, without IV-tPA or later treated with IV-tPA at 4 hours post-stroke. Cerebral blood flow (CBF) was measured by laser speckle contrast imaging (LSCI), behavioral outcomes as neurological deficit score (NDS) and adhesive tape removal test, and infarct size measurement were performed at 48 hours post-stroke. Mice within the experimental sets were randomized for the different treatments, and all outcome measures were blinded. RIPerC significantly improved CBF as measured by LSCI in both with and without tPA treated mice (P 
ISSN:2040-7378
2040-7378
DOI:10.1186/2040-7378-6-10