Key result
H2S-photothermal nanomedicine cuts aortic lesion areas by ~62% in preclinical atherosclerosis models.
Why the study?
Atherosclerosis is a primary cause of vascular diseases worldwide driven by multiple risk factors, making a comprehensive strategy to mitigate and reverse the disease imperative.
Does multifunctional UCST nanomedicine reduce atherosclerotic lesions in an atherosclerosis model?
Does multifunctional UCST nanomedicine reduce atherosclerotic lesions in an atherosclerosis model?
A novel UCST polymeric H2S-donor nanomedicine effectively reduces atherosclerotic plaque burden and improves lipid metabolism in a preclinical model.
Supports nanotherapy development in atherosclerosis models; leaves open human translation pending clinical trials.
Atherosclerosis (AS) stands as a primary cause of vascular diseases worldwide, with its occurrence and progression being attributed to the interplay of multiple risk factors. Therefore, it is imperative to develop a comprehensive strategy aimed at effectively mitigating and reversing AS. Herein, a hydrogen sulfide (H 2 S) donor is incorporated into a thermal‐sensitive polymer possessing an upper critical solution temperature (UCST), which not only serves as a novel macromolecular H 2 S donor but also forms the targeted nanocarrier for delivering a near infrared II photothermal agent, achieving the gas‐photothermal therapy against AS with notable advantages. For one aspect, the multifunctional UCST nanomedicine could target atherosclerotic plaque and perform the photoacoustic imaging‐guided H 2 S‐photothermal therapy to reduce the ratio of en‐face aortic lesion areas from 17.2% to 6.5% and alleviate the inflammatory AS microenvironment. For another aspect, the inevitable hepatic accumulation of UCST nanomedicine would activate the 5'‐adenosine monophosphate (AMP)‐activated protein kinase/mammalian target of rapamycin signaling pathway, thereby enhancing lipid metabolism and reducing plasma triglyceride levels. This transformation of waste nanomedicine into the valuable asset further aids in inhibiting the progression of AS. Consequently, the multifunctional UCST nanomedicine here would mediate an effective H 2 S‐photothermal therapy to attenuate AS.
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Ren et al. (2025) studied Atherosclerosis. UCST polymeric H2S-donor fabricated nanomedicine was evaluated on Ratio of en-face aortic lesion areas. Photoacoustic imaging-guided H2S-photothermal therapy using a multifunctional UCST nanomedicine reduced the ratio of en-face aortic lesion areas from 17.2% to 6.5% in atherosclerosis.
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