Effects of different obesogenic diets on joint integrity, inflammation and intermediate monocyte levels in a rat groove model of osteoarthritis

Journal Article (2023)
Author(s)

K. Warmink (University Medical Center Utrecht)

Jaqueline Lourdes Rios (University Medical Center Utrecht)

Devin R. van Valkengoed (University Medical Center Utrecht)

Prateeksha Vinod (University Medical Center Utrecht)

Nicoline M. Korthagen (University Medical Center Utrecht, Universiteit Utrecht)

H. Weinans (University Medical Center Utrecht, TU Delft - Biomaterials & Tissue Biomechanics)

Research Group
Biomaterials & Tissue Biomechanics
Copyright
© 2023 K. Warmink, J. L. Rios, D. R. van Valkengoed, P. Vinod, N. M. Korthagen, Harrie Weinans
DOI related publication
https://doi.org/10.3389/fphys.2023.1211972
More Info
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Publication Year
2023
Language
English
Copyright
© 2023 K. Warmink, J. L. Rios, D. R. van Valkengoed, P. Vinod, N. M. Korthagen, Harrie Weinans
Research Group
Biomaterials & Tissue Biomechanics
Volume number
14
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Abstract

Introduction: Obesogenic diets aggravate osteoarthritis (OA) by inducing low-grade systemic inflammation, and diet composition may affect OA severity. Here, we investigated the effect of diet on joint damage and inflammation in an OA rat model. Methods: Wistar-Han rats (n = 24) were fed a chow, a high-fat (HF) diet, or a high-fat/high-sucrose (HFS) for 24 weeks. OA was induced unilaterally 12 weeks after the diet onset by groove surgery, and compared to sham surgery or no surgical intervention (contralateral limb). Knee OA severity was determined by OARSI histopathology scoring system. At several timepoints monocyte populations were measured using flow cytometry, and joint macrophage response was determined via CD68 immunohistochemistry staining. Results: Groove surgery combined with HF or HFS diet resulted in higher OARSI scores, and both HF and HFS diet showed increased circulating intermediate monocytes compared to chow fed rats. Additionally, in the HFS group, minimal damage by sham surgery resulted in an increased OARSI score. HFS diet resulted in the largest metabolic dysregulation, synovial inflammation and increased CD68 staining in tibia epiphysis bone marrow. Conclusion: Obesogenic diets resulted in aggravated OA development, even with very minimal joint damage when combined with the sucrose/fat-rich diet. We hypothesize that diet-induced low-grade inflammation primes monocytes and macrophages in the blood, bone marrow, and synovium, resulting in joint damage when triggered by groove OA inducing surgery. When the metabolic dysregulation is larger, as observed here for the HFS diet, the surgical trigger required to induce joint damage may be smaller, or even redundant.