Shi Yingchao, Liu Chuanfen, Gui Yuesheng, Guo Yike, Zhang Yuanhao, Pan Jiangpeng, Tang Hao, Gao Chuanyu, Xing Junyue, Han Yu, Jiang Wei
Fuwai Central-China Cardiovascular Hospital, Central China Fuwai Hospital of Zhengzhou University, Zhengzhou, 450046, China.
National Health Commission Key Laboratory of Cardiovascular Regenerative Medicine, Central China Subcenter of National Center for Cardiovascular Diseases, Henan Cardiovascular Disease Center, Fuwai Central-China Cardiovascular Hospital, Central China Fuwai Hospital of Zhengzhou University, Zhengzhou, 450046, China.
Adv Healthc Mater. 2025 Mar;14(8):e2402763. doi: 10.1002/adhm.202402763. Epub 2024 Dec 15.
Acute myocardial infarction (MI) induced by thrombus formation is a prevalent cardiovascular disorder, and thrombolytic therapy continues to be a principal treatment modality. Prior research indicates a substantial association among MI, thrombosis, and the activation of oxidative stress pathways. The effectiveness of current thrombolytic drugs is relatively constrained, and the need for innovative and versatile thrombolytic medications remains critical. Nattokinase (NK) is a naturally-occurring enzyme known for its thrombolytic characteristics. Nonetheless, nattokinase's limited stability and susceptibility to inactivation in biological systems have impeded its clinical utility. This study designs a manganese oxide nanozyme (MnOx) loaded with NK (MnOx@NK), which exhibits both antioxidant and thrombolytic function. The administration of MnOx@NK through tail vein injection significantly restores vascular function and further reduces myocardial injury in a mouse model of myocardial infarction, demonstrating a pronounced protective effect against oxidative stress. These findings indicate that nattokinase-loaded nanozymes can be a promising approach for treating acute myocardial infarction, providing a new strategy for clinical application.
由血栓形成引起的急性心肌梗死(MI)是一种常见的心血管疾病,溶栓治疗仍然是主要的治疗方式。先前的研究表明,心肌梗死、血栓形成和氧化应激途径的激活之间存在密切关联。目前溶栓药物的有效性相对受限,因此对创新且多功能的溶栓药物的需求仍然至关重要。纳豆激酶(NK)是一种具有溶栓特性的天然存在的酶。然而,纳豆激酶在生物系统中的稳定性有限且易失活,这阻碍了其临床应用。本研究设计了一种负载纳豆激酶的氧化锰纳米酶(MnOx@NK),它兼具抗氧化和溶栓功能。通过尾静脉注射给予MnOx@NK可显著恢复血管功能,并进一步减轻心肌梗死小鼠模型中的心肌损伤,显示出对氧化应激有明显的保护作用。这些发现表明,负载纳豆激酶的纳米酶可能是治疗急性心肌梗死的一种有前景的方法,为临床应用提供了一种新策略。