J Appl Biomed 22:33-39, 2024 | DOI: 10.32725/jab.2024.002
Anti-inflammatory effect of luteoloside against methylglyoxal induced human dental pulp cells
- Jeonbuk National University, School of Dentistry, Institute of Oral Bioscience, Departments of Oral Biochemistry, Jeonju, Korea
Purpose: The aim of this study was to investigate whether luteoloside, a flavonoid, could protect human dental pulp cells (HDPCs) against inflammation and oxidative stress induced by methylglyoxal (MGO), one of the advanced glycated end products (AGE) substances.
Methods: HDPCs were stimulated with MGO and treated with luteoloside. MTT assay was used to determine cell viability. Protein expression was measured via western blotting. Reactive oxygen species (ROS) were measured with a Muse Cell Analyzer. Alkaline phosphatase activity (ALP) and Alizarin red staining were used for mineralization assay.
Results: Luteoloside down-regulated the expression of inflammatory molecules such as ICAM-1, VCAM-1, TNF-α, IL-1β, MMP-2, MMP-9, and COX-2 in MGO-induced HDPCs without showing any cytotoxicity. It attenuated ROS formation and enhanced osteogenic differentiation such as ALP activity and Alizarin red staining in MGO-induced HDPCs. Overall, luteoloside showed protective actions against inflammation and oxidative stress in HDPCs induced by MGO through its anti-inflammatory, anti-oxidative, and osteogenic activities by down-regulating p-JNK in the MAPK pathway.
Conclusion: These results suggest that luteoloside might be a potential adjunctive therapeutic agent for treating pulpal pathological conditions in patients with diabetes mellitus.
Keywords: Advanced glycated end product; Diabetes mellitus; Mineralization; Osteogenesis; Oxidative stress; Pulpitis
Grants and funding:
This work was supported by a grant from the National Research Foundation (NRF) of Korea, funded by the Korean government (MSIP) (NRF-2021R1F1A1049585).
Conflicts of interest:
The authors have no conflict of interest to declare.
Received: July 14, 2023; Revised: December 21, 2023; Accepted: February 12, 2024; Prepublished online: February 14, 2024; Published: March 15, 2024 Show citation
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