Tan Lishan, Zhou Huisong, Lai Zhiwei, Yang Guang, Zheng Fengping, Xiao Fei, Xiong Zuying, Huang Xiaoyan, Xiong Zibo
Department of Nephrology, Peking University Shenzhen Hospital, Shenzhen 518000, China.
Department of Nephrology, Peking University Shenzhen Hospital, Shenzhen 518000, China; Department of Nephrology, Wenjiang District People's Hospital, Chengdu 610203, China.
Nanomedicine. 2025 Jun;66:102819. doi: 10.1016/j.nano.2025.102819. Epub 2025 Mar 31.
Mitigation of adriamycin (ADR)-induced nephropathy remains a significant challenge in clinical management. Brain-targeted administration of losartan demonstrates comparable nephroprotective effects at a 1:500 concentration relative to gavage administration. This study established an exosome-based nano-delivery platform (ExoACP) to reduce drug dosage for alleviating ADR-induced nephropathy. The platform was rigorously tested for toxicity and blood-brain barrier penetration. Additionally, the role and possible mechanism of ExoACP-Los in alleviating ADR-induced nephropathy in mice were investigated. ExoACP showed enhanced penetration in brain microvascular endothelial cells, with a 7.20-fold increase in uptake. In the ADR model, ExoACP-Los exhibited anti-inflammatory and anti-fibrotic effects by downregulating the renin-angiotensin system, reducing extracellular matrix deposition by nearly half. These findings suggest ExoACP-Los can alleviate ADR-induced nephropathy by enhancing targeted drug delivery to the brain while reducing losartan. Overall, ExoACP holds significant potential for future clinical applications in chronic nephropathy.
减轻阿霉素(ADR)诱导的肾病在临床管理中仍然是一项重大挑战。与灌胃给药相比,脑靶向给药的氯沙坦在浓度为1:500时表现出相当的肾保护作用。本研究建立了一种基于外泌体的纳米递送平台(ExoACP),以减少药物剂量来减轻ADR诱导的肾病。该平台经过了严格的毒性和血脑屏障穿透测试。此外,还研究了ExoACP-Los在减轻小鼠ADR诱导的肾病中的作用及可能机制。ExoACP在脑微血管内皮细胞中的穿透能力增强,摄取量增加了7.20倍。在ADR模型中,ExoACP-Los通过下调肾素-血管紧张素系统表现出抗炎和抗纤维化作用,使细胞外基质沉积减少了近一半。这些发现表明,ExoACP-Los可以通过增强向脑的靶向药物递送同时减少氯沙坦来减轻ADR诱导的肾病。总体而言,ExoACP在慢性肾病的未来临床应用中具有巨大潜力。