ORIGINAL RESEARCH article
Front. Cell. Infect. Microbiol.
Sec. Oral Microbes and Host
Olanzapine affects bone formation via oral Enterococcus through SAA1 gene and extracellular matrix-related pathways
Provisionally accepted- Second Xiangya Hospital, Central South University, Changsha, China
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Background: Olanzapine is a commonly used drug in the treatment of schizophrenia, but the mechanism of abnormal bone metabolism caused by olanzapine is still unclear. The change of microflora may be an important factor leading to the change of bone metabolism. Therefore, the purpose of this study was to explore a plausible hypothesis that olanzapine may aggravate abnormal bone metabolism and cause bacterial imbalance in patients with schizophrenia. Methods: This study intervened in mice by gavage with olanzapine to detect changes in alveolar bone tissue and oral microbiota. The effect of related bacteria on osteogenesis were further examined. Results: The results showed that Enterococcus increased, the bone mass and type I collagen of alveolar bone decreased. Enterococcus lipoteichoic acid (LTA) inhibited osteogenic differentiation and up-regulated SAA1 gene expression. SAA1 gene can down-regulate the expression of COL1A1 gene, and the proteins encoded by the two may interact. Conclusions: Olanzapine may increase the relative abundance of oral Enterococcus, whose components are plausibly linked to increased expression of SAA1 gene and inhibition of bone formation through extracellular matrix-related pathways. These exploratory findings support further exploration of microbiota-based strategies to alleviate skeletal complications and promote oral health. Trial registration: The clinical research presented in this paper has been registered on ClinicalTrials.gov, a platform of the U.S. National Institutes of Health (Registration Number: NCT06123897; URL: https://clinicaltrials.gov/ct2/show/NCT06123897), with the registration date of November 9, 2023.
Keywords: olanzapine, oral Enterococcus, Bone formation, Serum amyloid A1 gene, Extracellular Matrix
Received: 26 Jul 2025; Accepted: 19 Nov 2025.
Copyright: © 2025 Yuan, Wang, Liu, Sreekissoon, Liu, Tan, Zhao, Zhong, Zhang, Su, Chen, Wang, Yang, Li, Zheng, Chen, Feng, Zhang and Guo. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Feng-Yi Zhang, kqzhangfengyi@csu.edu.cn
Yue Guo, guoyue@csu.edu.cn
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
