Kim Eun-Hye, Park Sehyeon, Bae Ok-Nam
College of Pharmacy, Kyungsung University, Busan 48434, Republic of Korea.
College of Pharmacy, Institute of Pharmaceutical Science and Technology, Hanyang University, Ansan 15588, Republic of Korea.
Int J Mol Sci. 2025 Jun 17;26(12):5816. doi: 10.3390/ijms26125816.
The rapid development of nanotechnology has led to increased human exposure to metal-based nanoparticles (MNPs) through inhalation, ingestion, and dermal contact, raising growing concerns on their potential health effects. Due to their nanoscale size and unique physicochemical properties, the MNPs can translocate from the initial exposure sites to the circulatory system and accumulate in the body. This review focuses on MNP-induced cardiovascular toxicity, highlighting its biodistribution, cytotoxic mechanisms, and pathological impact associated with various cardiovascular diseases. MNPs disrupt endothelial function, promote oxidative stress, and induce apoptosis and ferroptosis in cardiovascular cells. Furthermore, MNPs increase endothelial permeability, impair blood-brain barrier integrity, and enhance procoagulant activity, thereby contributing to vascular and cardiac dysfunction. The particles and their released metal ions play a synergistic role in mediating these toxic effects. Here, we focused on the effects of nano-sized particles while incorporating recent in vitro and in vivo studies that address the cardiovascular impacts and mechanisms of MNP-induced toxicity. This comprehensive review will help understand and explain the potentially toxic effects of MNPs on the cardiovascular system.
纳米技术的迅速发展导致人类通过吸入、摄入和皮肤接触更多地暴露于金属基纳米颗粒(MNPs),这引发了人们对其潜在健康影响的日益关注。由于MNPs的纳米级尺寸和独特的物理化学性质,它们可以从初始暴露部位转移到循环系统并在体内蓄积。本综述聚焦于MNPs诱导的心血管毒性,重点阐述其生物分布、细胞毒性机制以及与各种心血管疾病相关的病理影响。MNPs破坏内皮功能,促进氧化应激,并诱导心血管细胞凋亡和铁死亡。此外,MNPs增加内皮通透性,损害血脑屏障完整性,并增强促凝活性,从而导致血管和心脏功能障碍。这些颗粒及其释放的金属离子在介导这些毒性作用中发挥协同作用。在此,我们在纳入近期关于MNPs心血管影响及毒性机制的体外和体内研究的同时,重点关注纳米级颗粒的影响。这一全面综述将有助于理解和解释MNPs对心血管系统的潜在毒性作用。