Atherosclerosis is a common cardiovascular disease with
increasing
morbidity and mortality. The pathogenesis of atherosclerosis is strongly
related to endothelial dysfunction, which is induced by severe oxidative
stress damage derived from reactive oxygen species (ROS). Thus, ROS
plays a critical role in the pathogenesis and progression of atherosclerosis.
In this work, we demonstrated that the gadolinium doping of CeO2 (Gd/CeO2) nanozymes as effective ROS scavengers
delivered high performance for antiatherosclerosis. It was found that
the chemical doping of Gd promoted the surface proportion of Ce3+ in the nanozymes and thereby enhanced the overall ROS scavenging
ability. In vitro and in vivo experiments unambiguously showed that
the Gd/CeO2 nanozymes efficiently scavenged harmful ROS
at the cellular and histological levels. Further, Gd/CeO2 nanozymes were demonstrated to significantly reduce vascular lesions
by reducing lipid accumulation in macrophage and decreasing inflammatory
factor levels, thereby inhibiting the exacerbation of atherosclerosis.
Moreover, Gd/CeO2 can serve as T
1-weighted magnetic resonance imaging contrast agents, which can generate
sufficient contrast to distinguish the location of plaque during living
imaging. Through those efforts, Gd/CeO2 may serve as a
potential diagnostic and treatment nanomedicine for the ROS-induced
atherosclerosis.