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

Authors :
Chen, Bai-lu
Zang, Xin-yi
Mo, Jia-rong
Zhang, Ruo-yi
Wang, Heng
Wang, Quan-xi
Li, Jian
Source :
Frontiers in Cellular & Infection Microbiology; 2025, p1-14, 14p
Publication Year :
2025

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22352988
Database :
Complementary Index
Journal :
Frontiers in Cellular & Infection Microbiology
Publication Type :
Academic Journal
Accession number :
181981648
Full Text :
https://doi.org/10.3389/fcimb.2024.1423760