A GP130-Targeting Small Molecule, LMT-28, Reduces LPS-Induced Bone Resorption around Implants in Diabetic Models by Inhibiting IL-6/GP130/JAK2/STAT3 Signaling

Bibliographic Details
Title: A GP130-Targeting Small Molecule, LMT-28, Reduces LPS-Induced Bone Resorption around Implants in Diabetic Models by Inhibiting IL-6/GP130/JAK2/STAT3 Signaling
Authors: Qi-qi Liu, Wei-wei Wu, Jian Yang, Rui-bin Wang, Ling-ling Yuan, Pei-zhao Peng, Mao-yun Zeng, Ke Yu
Source: Mediators of Inflammation, Vol 2023 (2023)
Publisher Information: Wiley, 2023.
Publication Year: 2023
Collection: LCC:Pathology
Subject Terms: Pathology, RB1-214
More Details: In this study, we examined the effect of the GP130-targeting molecule, LMT-28, on lipopolysaccharide- (LPS-) induced bone resorption around implants in diabetic models using in vitro and rat animal experiments. First, LMT-28 was added to osteoblasts stimulated by LPS and advanced glycation end products (AGEs), and nuclear factor-κB receptor-activating factor ligand (RANKL) and associated pathways were evaluated. Then, LMT-28 was administered by gavage at 0.23 mg/kg once every 5 days for 2 weeks to type 2 diabetic rats with peri-implantitis induced by LPS injection and silk ligature. The expression of IL-6 and RANKL was evaluated by immunohistochemistry, and the bone resorption around implants was evaluated by microcomputed tomography. The results showed that LMT-28 downregulated the expression of RANKL through the JAK2/STAT3 signaling pathway in osteoblasts stimulated by LPS and AGEs, reduced bone resorption around implants with peri-implantitis, decreased the expression of IL-6 and RANKL, and decreased osteoclast activity in type 2 diabetic rats. This study confirmed the ability of LMT-28 to reduce LPS-induced bone resorption around implants in diabetic rats.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1466-1861
Relation: https://doaj.org/toc/1466-1861
DOI: 10.1155/2023/9330439
Access URL: https://doaj.org/article/01cfe5bd5507465aad1be8dcdb18a0b0
Accession Number: edsdoj.01cfe5bd5507465aad1be8dcdb18a0b0
Database: Directory of Open Access Journals
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More Details
ISSN:14661861
DOI:10.1155/2023/9330439
Published in:Mediators of Inflammation
Language:English