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辛伐他汀载药聚合物纳米粒:靶向炎症性巨噬细胞治疗肥胖症中局部脂肪组织褐变。

Simvastatin-Loaded Polymeric Nanoparticles: Targeting Inflammatory Macrophages for Local Adipose Tissue Browning in Obesity Treatment.

机构信息

Terasaki Institute for Biomedical Innovation, Los Angeles, California 90064, United States.

Department of Surgery, University of California-Los Angeles, Los Angeles, California 90095, United States.

出版信息

ACS Nano. 2024 Oct 8;18(40):27764-27781. doi: 10.1021/acsnano.4c10742. Epub 2024 Sep 29.

DOI:10.1021/acsnano.4c10742
PMID:39342648
Abstract

Obesity is defined as chronic, low-grade inflammation within specific tissues. Given the escalating prevalence of obesity among individuals of all ages, obesity has reached epidemic proportions, posing an important public health challenge. Despite significant advancements in treating obesity, conventional approaches remain largely ineffective or involve severe side effects, thus underscoring the pressing need to explore and develop treatment approaches. Targeted and local immunomodulation using nanoparticles (NPs) can influence fat production and utilization processes. Statins, known for their anti-inflammatory properties, show the potential for mitigating obesity-related inflammation. A localized delivery option offers several advantages over oral and parenteral delivery methods. Here, we developed simvastatin (Sim) encapsulated within PLGA NPs (Sim-NP) for localized delivery of Sim to adipose tissues (ATs) for immunomodulation to treat obesity. In vitro experiments revealed the strong anti-inflammatory effects of Sim-NPs, which resulted in enhanced modulation of macrophage (MΦ) polarization and induction of AT browning. We then extended our investigation to an mouse model of high-fat-diet (HFD)-induced obesity. Sim-NP administration led to the controlled release of Sim within AT, directly impacting MΦ activity and inducing AT browning while inducing weight loss. Our findings demonstrated that Sim-NP administration effectively inhibited the progression of obesity-related inflammation, controlled white fat production, and enhanced AT modulation. These results highlight the potential of Sim-NP as a potent nanotherapy for treating obesity by modulating the immune system.

摘要

肥胖被定义为特定组织中的慢性、低度炎症。鉴于各年龄段人群中肥胖症的患病率不断上升,肥胖症已达到流行程度,这对公共健康构成了重大挑战。尽管在治疗肥胖症方面取得了重大进展,但传统方法在很大程度上仍然无效或涉及严重的副作用,因此迫切需要探索和开发治疗方法。使用纳米颗粒(NPs)进行靶向和局部免疫调节可以影响脂肪的产生和利用过程。他汀类药物以其抗炎特性而闻名,显示出减轻肥胖相关炎症的潜力。局部递送方法比口服和肠胃外递送方法具有多项优势。在这里,我们开发了包封在 PLGA NPs 中的辛伐他汀(Sim)(Sim-NP),用于将 Sim 局部递送至脂肪组织(AT)以进行免疫调节来治疗肥胖症。体外实验揭示了 Sim-NP 的强大抗炎作用,导致巨噬细胞(MΦ)极化的增强调节和 AT 褐变的诱导。然后,我们将研究扩展到高脂肪饮食(HFD)诱导的肥胖小鼠模型。Sim-NP 给药导致 Sim 在 AT 内的控制释放,直接影响 MΦ 活性并诱导 AT 褐变,同时诱导体重减轻。我们的研究结果表明,Sim-NP 给药可有效抑制肥胖相关炎症的进展,控制白色脂肪的产生,并增强 AT 的调节。这些结果强调了 Sim-NP 通过调节免疫系统作为治疗肥胖症的有效纳米疗法的潜力。

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