Key result
IV N-acetylcysteine promotes lysis of treatment-resistant arterial thrombi and improves stroke outcomes in mice.
Why the study?
Does intravenous N-acetylcysteine promote lysis of arterial thrombi in experimental models of thrombosis?
Does intravenous N-acetylcysteine promote lysis of arterial thrombi in experimental models of thrombosis?
N-acetylcysteine demonstrates potent thrombolytic effects on arterial thrombi by cleaving VWF multimers, offering a potential alternative or adjunct to current antithrombotic agents.
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 MRI 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 prohemorrhagic 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 cross-link platelets in arterial thrombi. Coadministration of NAC and a nonpeptidic GpIIb/IIIa inhibitor further improved its thrombolytic efficacy, essentially by accelerating thrombus dissolution and preventing rethrombosis. Thus, in a new large-vessel thromboembolic stroke model in mice, this cotreatment significantly improved ischemic lesion size and neurological outcome. It is important to note that 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.
No takes yet. Share an insight, caveat, or question.
Lizarrondo et al. (2017) studied Arterial thrombosis. N-Acetylcysteine was evaluated on Lysis of arterial thrombi. Intravenous N-Acetylcysteine promoted lysis of arterial thrombi resistant to conventional treatments and improved ischemic lesion size and neurological outcomes in a mouse stroke model.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: