Fu Hairong, Li Xiaoshan, Tan Jiahua
Department of Physiology, Chongqing Three Gorges Medical College, Chongqing 404120, P.R. China.
Department of Pathology, Chongqing Three Gorges Medical College, Chongqing 404120, P.R. China.
Oncol Lett. 2018 Apr;15(4):4827-4836. doi: 10.3892/ol.2018.7922. Epub 2018 Feb 1.
The main method for the treatment of acute myocardial infarction (AMI) is percutaneous coronary intervention; however percutaneous coronary intervention will induce ischemia/reperfusion (IR) injury, resulting in the loss of cardiac function and cardiomyocyte death. An effective drug to target this condition is necessary. N-isopropylacrylamide and methacrylic acid were used to synthesize drug delivery nanoparticles (NP) containing the natural compound visnagin for IR injury treatment. It was demonstrated that NP containing fluorescein isothiocyanate localized to the site of myocardial IR, and that NP-visnagin treatment induced cardioprotection, reducing the size of the MI and ameliorating cardiac dysfunction through the induction of autophagy and the inhibition of apoptosis. In the future, visnagin may be suitable as a drug for IR injury treatment, and NP may be an effective drug delivery system.
急性心肌梗死(AMI)的主要治疗方法是经皮冠状动脉介入治疗;然而,经皮冠状动脉介入治疗会引发缺血/再灌注(IR)损伤,导致心功能丧失和心肌细胞死亡。因此,需要一种有效的药物来针对这种情况。使用N-异丙基丙烯酰胺和甲基丙烯酸合成了含有天然化合物紫铆因的药物递送纳米颗粒(NP),用于治疗IR损伤。结果表明,含有异硫氰酸荧光素的NP定位于心肌IR部位,并且NP-紫铆因治疗具有心脏保护作用,通过诱导自噬和抑制凋亡来减小心肌梗死面积并改善心脏功能障碍。未来,紫铆因可能适合作为IR损伤治疗药物,而NP可能是一种有效的药物递送系统。