Preparation, characterization, and protective effects of Gardenia fructus carbon dots against oxidative damage induced by LPS in IPEC-J2 cells

Front Cell Infect Microbiol. 2024 Dec 18:14:1423760. doi: 10.3389/fcimb.2024.1423760. eCollection 2024.

Abstract

This study aimed to prepare Gardenia fructus carbon dots (GF-CDs) and examine their efficacy in mitigating oxidative stress and apoptosis in intestinal porcine epithelial cells from the jejunum (IPEC-J2 cells) induced by lipopolysaccharide (LPS). The GF-CDs were synthesized using a one-step hydrothermal method. The oxidative damage model of IPEC-J2 cells was induced through LPS treatment. The potential mechanism by which GF-CDs affect cellular oxidative damage was examined through the perspectives of apoptosis, reactive oxygen species level, antioxidant-related enzyme index, mRNA transcription of antioxidant-related genes, and the expression of antioxidant proteins. The results revealed that GF-CDs, characterized by particle sizes<7 nm, abundant functional groups, and good water solubility, were synthesized using a one-step hydrothermal method. The carbon spots of Gardenia fructus at concentrations of 50, 100, and 200 μg/mL exhibited protective effects, as evidenced by their ability to enhance viability (P<0.01) and restore cellular morphology after oxidative damage. The GF-CDs decreased oxidative damage and reduced the apoptosis rate of cells by upregulating AKT1 expression and downregulating the expression of Caspase 3, STAT3, TNF-α, and JNK. These results indicate that GF-CDs have the characteristic physicochemical properties of CDs, exhibit biological activities related to antioxidation and cellular damage mitigation, and may serve as a potential healthcare product in swine raising.

Keywords: Gardenia fructus; IPEC-J2 cells; carbon dots; characterization; oxidative damage.

MeSH terms

  • Animals
  • Antioxidants* / pharmacology
  • Apoptosis* / drug effects
  • Carbon*
  • Caspase 3 / metabolism
  • Cell Line
  • Cell Survival / drug effects
  • Epithelial Cells* / drug effects
  • Epithelial Cells* / metabolism
  • Gardenia* / chemistry
  • Lipopolysaccharides*
  • Oxidative Stress* / drug effects
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology
  • Protective Agents / pharmacology
  • Reactive Oxygen Species* / metabolism
  • Swine
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Carbon
  • Lipopolysaccharides
  • Antioxidants
  • Reactive Oxygen Species
  • Tumor Necrosis Factor-alpha
  • Plant Extracts
  • Caspase 3
  • Protective Agents

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was supported by the Major Special Science and Technology of Fujian Province [Grant numbers: 2021NZ029008].