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[Circulation] Potent Thrombolytic Effect of N-Acetylcysteine on Arterial Thrombi


Abstract:

Background—Platelet crosslinking during arterial thrombosis involves von Willebrand Factor (VWF) multimers. Therefore, proteolysis of VWF appears promising to disaggregate platelet-rich thrombi and restore vessel patency in acute thrombotic disorders such as ischemic stroke, acute coronary syndrome or acute limb ischemia. N-Acetylcysteine (NAC, a clinically approved mucolytic drug) can reduce intrachain disulfide bonds in large polymeric proteins. In the present study, we postulated that NAC might cleave the VWF multimers inside occlusive thrombi, thereby leading to their dissolution and arterial recanalization.

Methods—Experimental models of thrombotic stroke induced by either intra-arterial thrombin injection or ferric chloride application followed by measurement of cerebral blood flow using a combination of laser Doppler flowmetry and magnetic resonance imaging were performed to uncover the effects of NAC on arterial thrombi. To investigate the effect of NAC on larger vessels, we also performed ferric chloride induced carotid artery thrombosis. In vitro experiments were performed to study the molecular bases of NAC thrombolytic effect, including platelet aggregometry, platelet-rich thrombi lysis assays, thromboelastography (ROTEM) and high shear VWF string formation using microfluidic devices. We also investigated the putative pro-hemorrhagic effect of NAC in a mouse model of intracranial hemorrhage induced by in situ collagenase type VII injection.

Results—We demonstrated that intravenous NAC administration promotes lysis of arterial thrombi that are resistant to conventional approaches such as recombinant tissue-type plasminogen activator, direct thrombin inhibitors and antiplatelet treatments. Through in vitro and in vivo experiments, we provide evidence that the molecular target underlying the thrombolytic effects of NAC is principally the VWF that crosslink platelets in arterial thrombi. Co-administration of NAC and a non peptidic GpIIb/IIIa inhibitor further improved its thrombolytic efficacy, essentially by accelerating thrombus dissolution and preventing re-thrombosis. Thus, in a new large vessel thromboembolic stroke model in mice, this co-treatment significantly improved ischemic lesion size and neurological outcome. Importantly, NAC did not worsen hemorrhagic stroke outcome, suggesting that it exerts thrombolytic effects without significantly impairing normal hemostasis.

Conclusions—We provide evidence that NAC is an effective and safe alternative to currently available antithrombotic agents to restore vessel patency after arterial occlusion.

Sara Martinez de Lizarrondo, Clément Gakuba, Bradley A. Herbig, Yohann Repessé, Carine Ali, Cécile V. Denis, Peter Lenting, Emmanuel Touzé, Scott L. Diamond, Denis Vivien, Maxime Gauberti https://doi.org/10.1161/CIRCULATIONAHA.117.027290 Circulation. 2017;CIRCULATIONAHA.117.027290 Originally published May 9, 2017

Link: http://circ.ahajournals.org/content/early/2017/05/09/CIRCULATIONAHA.117.027290.long

#05132017 #labonachip #Biologicalapplication

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