Multifunctional Prussian blue nanozymes alleviate atherosclerosis through inhibiting the inflammation feedback loop
Maochang Xu1, Dan Ran2, Jian Hu3,4
1Department of Pharmaceutical Sciences, School of Pharmacy, Southwest Medical University, Luzhou, Sichuan 646000, China. lispringhong@126.com.
Journal of Materials Chemistry. B
|December 18, 2024
Summary
This study introduces BSA@PB/Cur, a novel nanozyme that effectively clears reactive oxygen species (ROS) and reduces inflammation. It shows promise in treating atherosclerosis by targeting plaque lipid content and inflammatory feedback loops.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Cardiovascular Research
Background:
- Atherosclerosis (AS) is a chronic inflammatory disease driven by lipids, reactive oxygen species (ROS), and proinflammatory cytokines, creating a positive feedback loop in plaques.
- Traditional nanozymes have limitations in addressing the complex inflammatory and lipid-driven nature of AS.
- Prussian blue (PB) nanozymes offer potential due to ROS scavenging, anti-inflammatory properties, and photothermal effects aiding lipid removal from foam cells.
Purpose of the Study:
- To synthesize and evaluate a multifunctional nanozyme, BSA@PB/Cur, for atherosclerosis treatment.
- To investigate the in vitro and in vivo efficacy of BSA@PB/Cur in mitigating AS hallmarks.
- To explore the potential of BSA@PB/Cur in disrupting the inflammatory feedback loop within the atherosclerotic plaque microenvironment.
Main Methods:
- Synthesis of the multifunctional nanozyme BSA@PB/Cur via self-assembly of bovine serum albumin (BSA) with Prussian blue (PB) and encapsulation of curcumin (Cur).
- In vitro assessment of ROS scavenging, inhibition of inflammatory cytokines (TNF-α, IL-1β), and enhancement of cholesterol efflux in foam cells.
- In vivo evaluation of plaque targeting, lipid efflux, and matrix metalloproteinase expression in an atherosclerosis model.
Main Results:
- In vitro studies demonstrated BSA@PB/Cur's ability to scavenge ROS, reduce TNF-α and IL-1β expression, and promote cholesterol efflux by enhancing ABCA1 and ABCG1 expression, thereby inhibiting foam cell formation.
- In vivo experiments showed that BSA@PB/Cur effectively targeted plaques, significantly reduced lipid content, and decreased matrix metalloproteinase expression.
- The nanozyme demonstrated significant potential in alleviating the inflammatory positive feedback loop characteristic of atherosclerotic plaques.
Conclusions:
- BSA@PB/Cur is a multifunctional nanozyme with significant potential for treating atherosclerosis.
- The nanozyme effectively addresses key pathological features of AS, including ROS, inflammation, and lipid accumulation.
- This study presents a promising therapeutic strategy for managing the complex plaque microenvironment in atherosclerosis.
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