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贯叶金丝桃来源的外泌体样纳米囊泡用于脂肪组织光动力治疗。

Hypericum perforatum-derived exosomes-like nanovesicles for adipose tissue photodynamic therapy.

机构信息

Faculty of Chinese Medicine, Macau University of Science and Technology, Avenida Wai Long, Taipa, Macau, China; State Key Laboratory of Quality Research in Chinese Medicine (Macau University of Science and Technology), Avenida Wai Long, Taipa, Macau, China; Laboratory for Cardiovascular Pharmacology, Department of Pharmacology, School of Pharmacy, Basic Medicine Research Innovation Center for Cardiometabolic Diseases, Luzhou Municipal Key Laboratory of Thrombosis and Vascular Biology, Ministry of Education, Southwest Medical University, Luzhou, Sichuan 646000, China.

Department of Rheumatology and Immunology, Chongqing Emergency Medical Center, Chongqing University Central Hospital, Chongqing 400014, China.

出版信息

Phytomedicine. 2024 Sep;132:155854. doi: 10.1016/j.phymed.2024.155854. Epub 2024 Jul 6.

Abstract

BACKGROUND

Recent investigations underscore the capacity of photodynamic therapy (PDT) to induce adipocyte apoptosis, thereby mitigating obesity. Nonetheless, extant synthetic photosensitizers manifest limitations that hinder their clinical viability.

PURPOSE

In the current study, we used Hypericum perforatum-derived exosomes-like nanovesicles (HPExos) as a novel photosensitizer, and investigated its PDT effects in adipose tissue during obesity.

METHOD

HPExos-were administered to high fat diet mice via intraperitoneal injection, followed by targeted irradiation with specialized LED lights. Mass spectrometric analysis was analyzed in adipose tissues. CCK8 assay and Oil Red O staining were used to investigate lipid accumulation in 3T3-L1 cells to clarify adipocyte differentiation. The expression levels of related markers associated with adipogenesis and lipogenesis were assessed by RT-PCR. Apoptosis analysis was performed by TUNEL staining of and western blotting.

RESULTS

HPExos combined with PDT accumulated in visceral white adipose tissues results in a reduced body weight and improved insulin sensitivity. HPExos combined with PDT induced apoptosis by driving high levels of ROS. In addition, HPExos combined with PDT significantly downregulated the expression of transcription factors, PPARγ, C/EBPα, and SREBP and lipogenesis protein FABP4 both in vitro and in vivo, associated with a decreased FFA levels.

CONCLUSION

These findings suggest that HPExos could act as an effective photosensitizer in regulating glucose hemostasis by inhibiting adipocyte differentiation and lipogenesis, offering a promising approach for obesity treatment.

摘要

背景

最近的研究强调了光动力疗法(PDT)诱导脂肪细胞凋亡从而减轻肥胖的能力。然而,现有的合成光敏剂存在限制,阻碍了它们的临床应用。

目的

在本研究中,我们使用贯叶金丝桃衍生的外泌体样纳米囊泡(HPExos)作为一种新型光敏剂,研究其在肥胖期间脂肪组织中的 PDT 效应。

方法

通过腹腔注射将 HPExos 给予高脂肪饮食小鼠,然后用专用 LED 灯进行靶向照射。对脂肪组织进行质谱分析。使用 CCK8 assay 和 Oil Red O 染色来研究 3T3-L1 细胞中的脂质积累,以阐明脂肪细胞分化。通过 RT-PCR 评估与脂肪生成和脂生成相关的标志物的表达水平。通过 TUNEL 染色和 Western blot 进行凋亡分析。

结果

HPExos 与 PDT 联合在内脏白色脂肪组织中积累,导致体重减轻和胰岛素敏感性提高。HPExos 与 PDT 联合通过驱动高水平的 ROS 诱导细胞凋亡。此外,HPExos 与 PDT 联合在体外和体内均显著下调转录因子 PPARγ、C/EBPα 和 SREBP 的表达以及脂生成蛋白 FABP4,并降低游离脂肪酸水平。

结论

这些发现表明,HPExos 可作为一种有效的光敏剂,通过抑制脂肪细胞分化和脂生成来调节葡萄糖稳态,为肥胖治疗提供了一种有前途的方法。

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