# Heat-Treated Lacticaseibacillus rhamnosus Strains Modulate Inflammatory and Metabolic Processes in In Vitro Systems Relevant to Canine Osteoarthritis

**Authors:** Laura Rago, Guillermo García-Lainez, Miren Maicas, Ester Pardo, Veronica Navarro, Jennifer Redondo, Ferran Balaguer, Roberto Martinez, Silvia Llopis, Agata Rybicka, Adrián Florit-Ruiz, Empar Chenoll, Patricia Martorell

PMC · DOI: 10.3390/cells15040336 · Cells · 2026-02-12

## TL;DR

Heat-treated Lacticaseibacillus rhamnosus strains may help reduce inflammation and support joint health in dogs, offering a new approach to managing osteoarthritis.

## Contribution

Identifies two heat-treated Lacticaseibacillus rhamnosus strains with anti-inflammatory and collagen-synthesizing properties in canine models.

## Key findings

- Heat-treated Lacticaseibacillus rhamnosus strains reduce inflammation and increase type II collagen synthesis in canine chondrocytes.
- The strains improve gut health, reduce fat accumulation, and enhance muscle function in Caenorhabditis elegans models.
- These findings suggest the strains could target multiple risk factors for canine osteoarthritis.

## Abstract

What are the main findings?
Heat-treated Lacticaseibacillus rhamnosus strains (PRIOME® JH and HT-PB01) exhibited anti-inflammatory activity and type II collagen synthesis in cultured canine chondrocytes.In Caenorhabditis elegans models, both strains mitigate intestinal permeability, reduce fat accumulation, and enhance muscle structure and functionality, suggesting their potential to reduce risk factors associated with osteoarthritis.

Heat-treated Lacticaseibacillus rhamnosus strains (PRIOME® JH and HT-PB01) exhibited anti-inflammatory activity and type II collagen synthesis in cultured canine chondrocytes.

In Caenorhabditis elegans models, both strains mitigate intestinal permeability, reduce fat accumulation, and enhance muscle structure and functionality, suggesting their potential to reduce risk factors associated with osteoarthritis.

What are the implications of the main findings?
These results identify PRIOME® JH and HT-PB01 as promising postbiotic candidates for further investigation regarding their potential benefit for canine joint health.This study provides a preclinical basis for future in vivo investigation aimed at evaluating postbiotic strategies to address multiple risk factors associated with canine osteoarthritis.

These results identify PRIOME® JH and HT-PB01 as promising postbiotic candidates for further investigation regarding their potential benefit for canine joint health.

This study provides a preclinical basis for future in vivo investigation aimed at evaluating postbiotic strategies to address multiple risk factors associated with canine osteoarthritis.

Canine osteoarthritis is a progressive degenerative joint condition characterized by inflammation, structural damage, pain, and impaired joint function. Osteoarthritis risk is influenced not only by well-established factors such as age, genetics, obesity and underlying arthropathies, but also by systemic conditions such as low-grade inflammation and sarcopenia. Current interventions are primarily focused on pain relief rather than mitigating physiological impairment, despite recent veterinary guidelines. In this study, several preclinical models were employed to identify postbiotic candidates with potential to promote canine joint health. An initial screening of nine heat-treated bacterial strains identified two Lacticaseibacillus rhamnosus strains, PRIOME® JH and HT-PB01, which demonstrated significant anti-inflammatory activity on canine chondrocytes. Further characterization revealed that these two strains significantly increased type II collagen synthesis in canine chondrocytes and modulate immune responses in canine macrophages, enhancing Interleukin-10 secretion over Interleukin-12. Additionally, both strains showed potential in mitigating risk factors such as gut inflammation and permeability, fat accumulation and sarcopenia in Caenorhabditis elegans models. In conclusion, this study identified two promising postbiotic candidates, PRIOME® JH and HT-PB01, with the potential to target key risk factors associated with osteoarthritis through multifactorial mechanisms. These findings emphasize conducting dog clinical trials to evaluate their relevance in osteoarthritis.

## Linked entities

- **Proteins:** IL10 (interleukin 10)
- **Diseases:** osteoarthritis (MONDO:0005178)
- **Species:** Canis lupus familiaris (taxon 9615), Caenorhabditis elegans (taxon 6239)

## Full-text entities

- **Genes:** TGFB3 (transforming growth factor beta 3) [NCBI Gene 490796] {aka TGFbeta3}, COL2A1 (collagen type II alpha 1 chain) [NCBI Gene 403826], IGF2 (insulin like growth factor 2) [NCBI Gene 483664], IL10 (interleukin 10) [NCBI Gene 403628] {aka IL-10}, MMP1 (matrix metallopeptidase 1) [NCBI Gene 489428], VEGFA (vascular endothelial growth factor A) [NCBI Gene 403802] {aka VEGF}, IL1B (interleukin 1 beta) [NCBI Gene 403974] {aka IL-1}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 403850] {aka IL8}, IL6 (interleukin 6) [NCBI Gene 403985] {aka IL-6}, IGF1 (insulin like growth factor 1) [NCBI Gene 610255] {aka IGF-I, IGFI, IGFIA}, TNF (tumor necrosis factor) [NCBI Gene 403922] {aka TNFA, TNLG1F, cTNF}, ACAN (aggrecan) [NCBI Gene 403828] {aka AGC1, CSPCP}, rol-6 (Cuticle collagen rol-6) [NCBI Gene 174397]
- **Diseases:** tumor (MESH:D009369), atrophy (MESH:D001284), sarcopenia (MESH:D055948), Gut inflammation (MESH:D007249), injury to (MESH:D014947), autoimmune degenerative condition (MESH:D019636), pain (MESH:D010146), OA (MESH:D010003), fat (MESH:D004620), colorectal adenocarcinoma (MESH:D003110), cartilage (MESH:D002357), obese (MESH:D009765), gastrointestinal and renal complications (MESH:D005767), cytotoxicity (MESH:D064420), arthropathies (MESH:D007592), knee OA (MESH:D020370), osteoarthritic knees (MESH:D007718), stiffness disability (MESH:C566112), Gut damage (MESH:C536735), mobility impairment (MESH:D014086), HT (MESH:D018883), joint degradation (MESH:D055959), Hypertrophic (MESH:D002312), systemic (MESH:D015619)
- **Chemicals:** lactic acid (MESH:D019344), Streptomycin (MESH:D013307), NaCl (MESH:D012965), chondroitin sulfate (MESH:D002809), Nile red (MESH:C044808), Alginate (MESH:D000464), CaCl2 (MESH:D002122), MTX (MESH:D008727), dexamethasone (MESH:D003907), MTT (MESH:C070243), amino acids (MESH:D000596), DMEM (-), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MESH:C022616), Penicillin (MESH:D010406), Orlistat (MESH:D000077403), 5-Fluoro-2'-deoxyuridine (MESH:C576827), glucosamine (MESH:D005944), McCoy's 5A medium (MESH:C113109), L-Glutamine (MESH:D005973), BCA (MESH:C047117), CO2 (MESH:D002245), cysteine (MESH:D003545), LPS (MESH:D008070), agarose (MESH:D012685)
- **Species:** Caenorhabditis elegans (species) [taxon 6239], Mus musculus (house mouse, species) [taxon 10090], Lacticaseibacillus rhamnosus (species) [taxon 47715], Canis lupus familiaris (dog, subspecies) [taxon 9615], Escherichia coli (E. coli, species) [taxon 562], C. elegans [taxon 328850], Hungerfordia sp. T (species) [taxon 563708], Rattus norvegicus (brown rat, species) [taxon 10116], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Homo sapiens (human, species) [taxon 9606], Felis catus (cat, species) [taxon 9685], Bifidobacterium (genus) [taxon 1678], PB01 [taxon 426302], Cavia porcellus (domestic guinea pig, species) [taxon 10141]
- **Cell lines:** Cn402-05 — Rattus norvegicus (Rat), Rat malignant glioma, Cancer cell line (CVCL_S568), S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232), DH82 — Canis lupus familiaris (Dog), Canine histiocytic sarcoma, Cancer cell line (CVCL_2018), HT-29 — Homo sapiens (Human), Amyotrophic lateral sclerosis 1, Induced pluripotent stem cell (CVCL_8999), CRL-3590 — Homo sapiens (Human), Propionic acidemia, Finite cell line (CVCL_2N31)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939062/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12939062/full.md

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Source: https://tomesphere.com/paper/PMC12939062