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

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.

Keywords: Apoptosis; Exosomes-like nanovesicles; Hypericum perforatum; Obesity; Photodynamic therapy.

MeSH terms

  • 3T3-L1 Cells*
  • Adipocytes / drug effects
  • Adipogenesis / drug effects
  • Adipose Tissue / drug effects
  • Animals
  • Apoptosis* / drug effects
  • CCAAT-Enhancer-Binding Protein-alpha / metabolism
  • CCAAT-Enhancer-Binding Proteins
  • Diet, High-Fat
  • Exosomes* / metabolism
  • Fatty Acid-Binding Proteins
  • Hypericum* / chemistry
  • Insulin Resistance
  • Lipogenesis / drug effects
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Obesity* / drug therapy
  • PPAR gamma / metabolism
  • Photochemotherapy* / methods
  • Photosensitizing Agents / pharmacology
  • Plant Extracts / pharmacology
  • Reactive Oxygen Species / metabolism
  • Sterol Regulatory Element Binding Protein 1

Substances

  • Photosensitizing Agents
  • PPAR gamma
  • Fabp4 protein, mouse
  • CCAAT-Enhancer-Binding Protein-alpha
  • Reactive Oxygen Species
  • CEBPA protein, mouse
  • Srebf1 protein, mouse
  • Plant Extracts
  • CCAAT-Enhancer-Binding Proteins
  • Fatty Acid-Binding Proteins
  • Sterol Regulatory Element Binding Protein 1