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The Oral Administration of Subsp. 557 (LDL557) Ameliorates the Progression of Monosodium Iodoacetate-Induced Osteoarthritis

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Publisher MDPI
Specialty Molecular Biology
Date 2024 Aug 28
PMID 39194747
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Abstract

Low-grade body inflammation is a major cause of osteoarthritis (OA), a common joint disease. Gut dysbiosis may lead to systemic inflammation which can be prevented by probiotic administration. The subsp. 557 (LDL557) has been demonstrated to have beneficial effects for anti-inflammation. This study investigated the effects of LDL557 on OA progress using monosodium iodoacetate (MIA)-induced OA of rats. Live or heat-killed (HK)-LDL557 of a low or high dose was administrated for two weeks before MIA-induced OA, and then continuously administrated for another six weeks. After taking supplements for eight weeks, OA progress was analyzed. Results showed that MIA induced knee joint swelling, chondrocyte damage, and cartilage degradation, and supplementation with a high dose of LDL557 reduced MIA-induced knee joint swelling, chondrocyte damage, and cartilage degradation. Additionally, MIA increased serum levels of the matrix-degrading enzyme MMP-13, while a high dose of HK-LDL557 decreased it for the controls. Simultaneously, bone turnover markers and inflammatory cytokines of serum were assayed, but no significant differences were found except for a TNF-α decrease from a low dose of live LDL557. These results demonstrated that supplementation with high doses of live LDL557 or HK-LDL557 can reduce the progression of MIA-induced OA in rats.

Citing Articles

Heat-Killed subsp. 557 Extracts Protect Chondrocytes from Osteoarthritis Damage by Reducing Inflammation: An In Vitro Study.

Hu Y, Huang T, Hsieh B, Huang L, Lin J, Hsu H Nutrients. 2025; 16(24.

PMID: 39771038 PMC: 11676954. DOI: 10.3390/nu16244417.

References
1.
Pritzker K, Gay S, Jimenez S, Ostergaard K, Pelletier J, Revell P . Osteoarthritis cartilage histopathology: grading and staging. Osteoarthritis Cartilage. 2005; 14(1):13-29. DOI: 10.1016/j.joca.2005.07.014. View

2.
Fahy N, Farrell E, Ritter T, Ryan A, Murphy J . Immune modulation to improve tissue engineering outcomes for cartilage repair in the osteoarthritic joint. Tissue Eng Part B Rev. 2014; 21(1):55-66. PMC: 4321974. DOI: 10.1089/ten.TEB.2014.0098. View

3.
So J, Song M, Kwon H, Lee C, Chae C, Sahoo A . Lactobacillus casei enhances type II collagen/glucosamine-mediated suppression of inflammatory responses in experimental osteoarthritis. Life Sci. 2010; 88(7-8):358-66. DOI: 10.1016/j.lfs.2010.12.013. View

4.
Lin Y, Chang S, Liu S, Achudhan D, Tsai Y, Lin S . Therapeutic Effects of Live GKD7 in a Rat Model of Knee Osteoarthritis. Nutrients. 2022; 14(15). PMC: 9370768. DOI: 10.3390/nu14153170. View

5.
Sahin K, Kucuk O, Orhan C, Tuzcu M, Durmus A, Ozercan I . Niacinamide and undenatured type II collagen modulates the inflammatory response in rats with monoiodoacetate-induced osteoarthritis. Sci Rep. 2021; 11(1):14724. PMC: 8289820. DOI: 10.1038/s41598-021-94142-3. View