Soluble Nanomedicine Against Soluble Neurosensitizers to Effectively Relieve Osteoarthritis Pain and Joint Damage
9 affiliations
- 1Department of Orthopaedics The Third Xiangya Hospital Central South University Changsha China
- 2Department of Orthopaedics Xiangya Hospital Central South University Changsha China
- 3Xiangya School of Pharmaceutical Sciences Central South University Changsha China
- 4Department of Pharmacology and Chemical Biology College of Basic Medical Sciences Shanghai Jiao Tong University School of Medicine Shanghai China
- 5Department of Pharmacy Xiangya Hospital Central South University Changsha China
- 6Key Laboratory of Aging‐Related Bone and Joint Diseases Prevention and Treatment Ministry of Education Xiangya Hospital Central South University Changsha China
- 7Department of Endocrinology Endocrinology Research Center Xiangya Hospital of Central South University Changsha China
- 8Hunan Key Laboratory of Joint Degeneration and Injury Changsha China
- 9National Clinical Research Center for Geriatric Disorders Xiangya Hospital Central South University Changsha China
Abstract
Targeting soluble neurosensitizers in the osteoarthritis (OA) joint cavity is a key strategy for alleviating OA pain. Soluble neurosensitizers are ubiquitous in the joint cavity and cause uncontrollable growth and sensitization of nociceptor axons therein. However, eliminating these soluble nerve growth factors (NGFs) remains a considerable challenge due to the diversity of neurosensitizers and the complexity of OA pathology. This study introduces an innovative soluble nanodrug (LAC)‐based strategy to eliminate three key neurosensitizers (H+, NGF, and netrin‐1) to simultaneously relieve OA‐associated pain and joint damage. In two animal model experiments, LAC significantly reduced pain and alleviated OA progression by reducing synovial inflammation and inhibiting cartilage and subchondral bone damage. This strategy of using soluble nanomedicine to counter soluble neurosensitizers not only provides inspiration for eliminating pain, but also sheds light on possible solutions for advancing OA treatment strategies.
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BibTeX
@article{liu2026soluble,
title = {{Soluble Nanomedicine Against Soluble Neurosensitizers to Effectively Relieve Osteoarthritis Pain and Joint Damage}},
author = {Junyan Liu and Feixiang Ding and Jiayi Li and Min Liu and Lingyu Su and Zixi Wang and Congying Pi and Shilong Jiang and Zhaokui Zeng and Changjun Li and Chao Zeng and Guanghua Lei and Kelong Ai},
journal = {Exploration},
year = {2026},
month = oct,
doi = {10.1002/exp2.70233},
url = {https://doi.org/10.1002/exp2.70233},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Soluble Nanomedicine Against Soluble Neurosensitizers to Effectively Relieve Osteoarthritis Pain and Joint Damage
AU - Junyan Liu
AU - Feixiang Ding
AU - Jiayi Li
AU - Min Liu
AU - Lingyu Su
AU - Zixi Wang
AU - Congying Pi
AU - Shilong Jiang
AU - Zhaokui Zeng
AU - Changjun Li
AU - Chao Zeng
AU - Guanghua Lei
AU - Kelong Ai
PY - 2026
DA - 2026/10/08
JO - Exploration
DO - 10.1002/exp2.70233
UR - https://doi.org/10.1002/exp2.70233
AB - Targeting soluble neurosensitizers in the osteoarthritis (OA) joint cavity is a key strategy for alleviating OA pain. Soluble neurosensitizers are ubiquitous in the joint cavity and cause uncontrollable growth and sensitization of nociceptor axons therein. However, eliminating these soluble nerve growth factors (NGFs) remains a considerable challenge due to the diversity of neurosensitizers and the complexity of OA pathology. This study introduces an innovative soluble nanodrug (LAC)‐based strategy to eliminate three key neurosensitizers (H+, NGF, and netrin‐1) to simultaneously relieve OA‐associated pain and joint damage. In two animal model experiments, LAC significantly reduced pain and alleviated OA progression by reducing synovial inflammation and inhibiting cartilage and subchondral bone damage. This strategy of using soluble nanomedicine to counter soluble neurosensitizers not only provides inspiration for eliminating pain, but also sheds light on possible solutions for advancing OA treatment strategies.
SN - 2766-8509
SN - 2766-2098
ER -