Insulin growth factor binding protein-3 enhances dental implant osseointegration against methylglyoxal-induced bone deterioration in a rat model
Takanche Jyoti Shrestha, 김지은, 장성일, 이호근,
소속 상세정보
( Takanche Jyoti Shrestha ) - Chonbuk National University School of Dentistry Department of Oral Biochemistry
김지은 ( Kim Ji-Eun ) - Chonbuk National University School of Dentistry Department of Oral Biochemistry
장성일 ( Jang Sung-Il ) - Chonbuk National University School of Dentistry Department of Oral Biochemistry
이호근 ( Yi Ho-Keun ) - Chonbuk National University School of Dentistry Department of Oral Biochemistry
Abstract
Purpose: The aim of this study was to determine the effect of insulin growth factor binding protein-3 (IGFBP-3) on the inhibition of glucose oxidative stress and promotion of bone formation near the implant site in a rat model of methylglyoxal (MGO)-induced bone loss.
Methods: An in vitro study was performed in MC3T3 E1 cells treated with chitosan gold nanoparticles (Ch-GNPs) conjugated with IGFBP-3 cDNA followed by MGO. An in vivo study was conducted in a rat model induced by MGO administration after the insertion of a dental implant coated with IGFBP-3.
Results: MGO treatment downregulated molecules involved in osteogenic differentiation and bone formation in MC3T3 E1 cells and influenced the bone mineral density and bone volume of the femur and alveolar bone. In contrast, IGFBP-3 inhibited oxidative stress and inflammation and enhanced osteogenesis in MGO-treated MC3T3 E1 cells. In addition, IGFBP-3 promoted bone formation by reducing inflammatory proteins in MGO-administered rats. The application of Ch-GNPs conjugated with IGFBP-3 as a coating of titanium implants enhanced osteogenesis and the osseointegration of dental implants.
Conclusions: This study demonstrated that IGFBP-3 could be applied as a therapeutic component in dental implants to promote the osseointegration of dental implants in patients with diabetes, which affects MGO levels.
키워드
Antioxidants; Bone formation; Diabetes mellitus; Inflammation; MC3T3 E1
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