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Investigación Clínica
versión impresa ISSN 0535-5133versión On-line ISSN 2477-9393
Resumen
YE, Liangwen et al. Lycopene regulates the formation of calcium oxalate kidney stones by modulating reactive oxygen species(ROS) and NF-κB pathways. Invest. clín [online]. 2025, vol.66, n.2, pp.205-216. Epub 25-Jun-2025. ISSN 0535-5133. https://doi.org/10.54817/ic.v66n2a07.
This study aims to determine whether lycopene can reduce oxidative stress and inflammatory damage in HK-2 cell cultures induced by calcium oxalate crystallization through the modulation of reactive oxygen species (ROS) and the NF-κB signalling pathway. Cell cultures were divided into four groups: The control group, the Model group (COM + oxalic acid), and two Lycopene intervention groups (COM + oxalic acid + 5/10 μmol/L lycopene). After 24 hours of culture, viability, LDH, oxidative and anti-oxidative parameters, mitochondrial membrane potential, MCP-1, IL-6, apoptosis and related proteins, and activation and expression of NF-κB were determined by adequate methods. When compared to the control group, the model group exhibited decreased cell activity (p<0.001) and GSH and SOD antioxidant capacity (p<0.05), alongside a significant rise in LDH, MDA, and the release of inflammatory mediators MCP-1 and IL-6 (p<0.05). The levels of protein expression for NF-κB, OPN, Bax, Cyt C, and active Caspase-3 were increased (p<0.05), whereas Bcl-2 protein expression significantly diminished (p<0.05). The mitochondrial membrane potential decreased. Lycopene intervention reduced the damage to HK-2 cells (p<0.05), accompanied by decreased levels of LDH, MDA, and inflammatory factors MCP-1 and IL-6 (p<0.05), and increased GSH and SOD antioxidant capacity (p<0.05). The mitochondrial membrane potential was observed to in crease. No significant changes were observed in the expression of NF-κB. The expressions of OPN, Bax, Cyt C, and Caspase-3 decreased (p<0.05), whereas the level of Bcl-2 protein expression increased. In conclusion, lycopene decreases cellular damage by inhibiting lipid peroxidation induced by calcium oxalate crystals and oxalate, enhancing intracellular antioxidant enzyme activity, modulating ROS and NF-κB inflammatory pathways, improving mitochondrial integrity, and exerting anti-inflammatory effects through the inhibition of the mitochondrial-mediated Bax/Caspase-3 signalling pathway.
Palabras clave : lycopene; renal tubular epithelial cells; oxalic acid; reactive oxygen species; apoptosis.












