# Comparison of passive and active motion: effect of myokine irisin on cartilage in knee osteoarthritis rats

**Authors:** Zhengjiao Duan, Hongpan Gao, Xue Xiao, BenXiang He

PMC · DOI: 10.3389/fphys.2025.1639174 · Frontiers in Physiology · 2025-07-29

## TL;DR

This study compares active and passive motion in treating knee osteoarthritis in rats, finding that passive motion has stronger benefits for cartilage protection and muscle strength.

## Contribution

The study reveals that passive motion induces higher irisin levels and better chondroprotective effects than active motion in KOA rats.

## Key findings

- Passive motion (PAG) improved hindlimb grip strength and quadriceps weight more than active motion (AAG).
- Irisin levels were highest in PAG and negatively correlated with inflammatory cytokines like IL-6 and TNF-α.
- Both PAG and AAG reduced cartilage degradation markers (MMP-13, MMP-9) and improved cartilage appearance.

## Abstract

Knee osteoarthritis (KOA) severely impacts knee joint health. Irisin, a myokine secreted during muscle contraction, varies with different exercise. This study investigates the chondroprotective effects of irisin induced by active and passive motion in a rat model of KOA.

The rats were randomly allocated into control (CG), model (OAG), passive motion (PAG), and active motion groups (AAG). KOA was induced by intra-articular injections of monosodium iodoacetate (MIA) in all groups except CG. The PAG and AAG group underwent 4 weeks of treadmill exercise or quadriceps femoris muscle electroacupuncture. Changes in irisin, chondrocyte metabolic markers, and inflammatory factors were evaluated using ELISA, histology, immunohistochemistry, and qRT-PCR. Pearson correlation analysis was performed to assess the relationship between irisin and inflammatory factors.

One-week post-modeling, the OAG group showed the lowest hindlimb grip strength and quadriceps weight, chondrocyte number, collagen II expression and irisin levels, while displaying the highest levels of matrix-degrading enzymes (MMP-13, MMP-9, ADAMTS-5) and inflammatory factors (IL-6, TNF-α, IL-1β, IL-18). However, after 4 weeks of intervention, both the PAG and AAG groups reversed these trends. The PAG group exhibited greater improvements in hindlimb grip strength and quadriceps weight compared to the AAG group. HE staining, toluidine blue and safranin O showed smoother cartilage surfaces, increased cartilage thickness and stronger safranin O staining in PAG and AAG groups compared to OAG. Collagen II protein expression was upregulated (P < 0.001), while MMP–13 was downregulated (P < 0.001), and the mRNA levels of MMP-9 and ADAMTS-5 were downregulated (P < 0.001). Moreover, inflammatory factors were lower in PAG than in AAG. Irisin expression was highest in the PAG group, followed by AAG, CG, and OAG group, in serum, synovial fluid and cartilage. Irisin levels were negatively correlated with IL-6, TNF-α, IL-1β, and IL-18.

Both active and passive motion inhibited cartilage degeneration in KOA rats, with passive exercise showing superior effects on muscle strength, irisin secretion, and downregulation of inflammatory cytokines. The chondroprotective and anti-inflammatory effects were positively correlated with increased irisin expression.

## Linked entities

- **Proteins:** FNDC5 (fibronectin type III domain containing 5), MMP13 (matrix metallopeptidase 13), MMP9 (matrix metallopeptidase 9), ADAMTS5 (ADAM metallopeptidase with thrombospondin type 1 motif 5), IL6 (interleukin 6), TNF (tumor necrosis factor), IL1B (interleukin 1 beta), IL18 (interleukin 18)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Mmp13 (matrix metallopeptidase 13) [NCBI Gene 171052], Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}, Mmp9 (matrix metallopeptidase 9) [NCBI Gene 81687], Il18 (interleukin 18) [NCBI Gene 29197] {aka IL-1 gamma, IL-18}, Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, Adamts5 (ADAM metallopeptidase with thrombospondin type 1 motif, 5) [NCBI Gene 304135], Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}
- **Diseases:** cartilage degeneration (MESH:D002357), inflammatory (MESH:D007249), KOA (MESH:D020370)
- **Chemicals:** HE (MESH:D006371), toluidine blue (MESH:D014048), safranin O (MESH:C009195), MIA (MESH:D019807), OAG (-)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12339569/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12339569/full.md

## References

63 references — full list in the complete paper: https://tomesphere.com/paper/PMC12339569/full.md

---
Source: https://tomesphere.com/paper/PMC12339569