Oral Administration of Lactobacillus rhamnosus Ameliorates the Progression of Osteoarthritis by Inhibiting Joint Pain and Inflammation

被引:53
作者
Jhun, JooYeon [1 ,2 ]
Cho, Keun-Hyung [1 ,2 ]
Lee, Dong-Hwan [3 ]
Kwon, Ji Ye [1 ]
Woo, Jin Seok [1 ]
Kim, Jiyoung [1 ]
Na, Hyun Sik [1 ,2 ]
Park, Sung-Hwan [4 ]
Kim, Seok Jung [3 ]
Cho, Mi-La [1 ,5 ]
机构
[1] Catholic Univ Korea, Catholic Res Inst Med Sci, Rheumatism Res Ctr, Seoul 06591, South Korea
[2] Catholic Univ Korea, Dept Biomed & Hlth Sci, Coll Med, 222 Banpo Daero, Seoul 06591, South Korea
[3] Catholic Univ Korea, Uijeongbu St Marys Hosp, Dept Orthoped Surg, Coll Med, Seoul 06591, South Korea
[4] Catholic Univ Korea, Seoul St Marys Hosp, Div Rheumatol, Dept Internal Med,Coll Med, Seoul 06591, South Korea
[5] Catholic Univ Korea, Dept Med Lifesci, Coll Med, 222 Banpo Daero, Seoul 06591, South Korea
基金
新加坡国家研究基金会;
关键词
osteoarthritis; monosodium iodoacetate (MIA); inflammation; microbiota; Lactobacillus rhamnosus; PROBIOTICS; COLLAGEN;
D O I
10.3390/cells10051057
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Osteoarthritis (OA) is the most common form of arthritis and age-related degenerative joint disorder, which adversely affects quality of life and causes disability. However, the pathogenesis of OA remains unclear. This study was performed to examine the effects of Lactobacillus rhamnosus in OA progression. OA was induced in 6-week-old male Wistar rats by monosodium iodoacetate (MIA) injection, and the effects of oral administration of L. rhamnosus were examined in this OA rat model. Pain severity, cartilage destruction, and inflammation were measured in MIA-induced OA rats. The small intestines were isolated from OA rats, and the intestinal structure and inflammation were measured. Protein expression in the dorsal root ganglion was analyzed by immunohistochemistry. The effects of L. rhamnosus on mRNA and protein expression in chondrocytes stimulated with interleukin (IL)-1 beta and lipopolysaccharide (LPS) were analyzed by real-time polymerase chain reaction (RT-PCR) and enzyme-linked immunosorbent assay (ELISA). Pain severity was decreased in L. rhamnosus-treated MIA-induced OA rats. The levels of expression of MCP-1, a potential inflammatory cytokine, and its receptor, CCR2, were decreased, and GABA and PPAR-gamma expression were increased in L. rhamnosus-treated OA rats. The inflammation, as determined by IL-1 beta, and cartilage destruction, as determined by MMP3, were also significantly decreased by L. rhamnosus in OA rats. Additionally, intestinal damage and inflammation were improved by L. rhamnosus. In human OA chondrocytes, TIMP1, TIMP3, SOX9, and COL2A1 which are tissue inhibitors of MMP, and IL-10, an anti-inflammatory cytokine, were increased by L. rhamnosus. L. rhamnosus treatment led to decreased pain severity and cartilage destruction in a rat model of OA. Intestinal damage and inflammation were also decreased by L. rhamnosus treatment. Our findings suggested the therapeutic potential of L. rhamnosus in OA.
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页数:14
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