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Live and Dead Clostridium butyricum GKB7 Diminish Osteoarthritis Pain and Progression in Preclinical Animal Model.
Chen, Li-Chai; Lin, Yen-You; Tsai, You-Shan; Chen, Chin-Chu; Chang, Tzu-Ching; Chen, Hsien-Te; Hsu, Chin-Jung; Tang, Chih-Hsin.
Afiliação
  • Chen LC; Department of Pharmacy, Tajen University, Pingtung, Taiwan.
  • Lin YY; Department of Pharmacology, School of Medicine, China Medical University, Taichung, Taiwan.
  • Tsai YS; Biotech Research Institute, Grape King Bio Ltd., Taoyuan, Taiwan.
  • Chen CC; Biotech Research Institute, Grape King Bio Ltd., Taoyuan, Taiwan.
  • Chang TC; Institute of Food Science and Technology, National Taiwan University, Taipei, Taiwan.
  • Chen HT; Department of Pharmacology, School of Medicine, China Medical University, Taichung, Taiwan.
  • Hsu CJ; Department of Sports Medicine, College of Health Care, China Medical University, Taichung, Taiwan.
  • Tang CH; Department of Orthopedic Surgery, China Medical University Hospital, Taichung, Taiwan.
Environ Toxicol ; 2024 Jun 25.
Article em En | MEDLINE | ID: mdl-38923690
ABSTRACT
Osteoarthritis (OA) is a degenerative joint disease primarily affecting the elderly. It is characterized by the progressive decline of joint cartilage and alterations in the underlying bone. Several probiotic strains have exhibited immunomodulatory and anti-inflammatory properties. Here, we examined the functions of live and dead Clostridium butyricum GKB7 (GKB7-L and GKB7-D) in a preclinical anterior cruciate ligament transection (ACLT)-enhanced OA procedure. Oral administration of GKB7-L and GKB7-D ameliorated ACLT-induced bone pain as assessed by weight-bearing behavioral testing but did not affect body weight. Micro-computed tomography (CT) results showed that GKB7-L and GKB7-D diminished ACLT-induced bone destruction and loss. GKB7-L and GKB7-D-enriched therapies also reduced ACLT-induced production of the pro-inflammatory cytokines interleukin (IL)-1ß and tumor necrosis factor (TNF)-α, as well as the chondrolytic factor matrix metalloproteinase (MMP)-3, leading to inhibition of aggrecan and collagen type II degradation and thereby blocking cartilage breakdown. We therefore suggest that oral supplementation with GKB7-L or GKB7-D can be beneficial in the prevention and treatment of OA.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article