A Blend of Tamarindus Indica and Curcuma Longa Extracts Alleviates Monosodium Iodoacetate (MIA)-Induced Osteoarthritic Pain and Joint Inflammation in Rats

被引:2
作者
Kwon, Sae-Bom [1 ]
Chinta, Gopichand [2 ]
Kundimi, Sreenath [3 ]
Kim, Sangback [1 ]
Cho, Young-Dae [1 ]
Kim, Seul-Ki [1 ]
Ju, Jae-Yeong [1 ]
Sengupta, Krishanu [3 ,4 ]
机构
[1] Kolmar BNH Co LTD, Hlth Food Lab, Seoul, South Korea
[2] Laila Nutraceut R&D Ctr, Dept Pharmacol, Vijayawada, Andhra Prades, India
[3] Laila Nutraceut R&D Ctr, Dept Cell & Mol Biol, Vijayawada, Andhra Prades, India
[4] Laila Nutraceut R&D Ctr, JRD Tata Ind Estate, Vijayawada 520007, Andhra Prades, India
来源
JOURNAL OF THE AMERICAN NUTRITION ASSOCIATION | 2024年 / 43卷 / 01期
关键词
Monosodium iodoacetate (MIA)-induced osteoarthritis; joint pain and inflammation; cyclooxygenase-2; matrix metalloproteinases; EFFICACY; METAANALYSIS; PROGRESSION; MODEL;
D O I
10.1080/27697061.2023.2209880
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background and objective: NXT15906F6 (TamaFlex(TM)) is a proprietary herbal composition containing Tamarindus indica seeds and Curcuma longa rhizome extracts. NXT15906F6 supplementation has been shown clinically effective in reducing knee joint pain and improving musculoskeletal functions in healthy and knee osteoarthritis (OA) subjects. The objective of the present study was to assess the possible molecular basis of the anti-OA efficacy of NXT15906F6 in a monosodium iodoacetate (MIA)-induced model of OA in rats. Methods: Healthy male Sprague Dawley rats (age: 8-9 wk body weight, B.W.: 225-308 g (n = 12) were randomly assigned to one of the six groups, (a) vehicle control, (b) MIA control, (c) Celecoxib (10 mg/kg B.W.), (d) TF-30 (30 mg/kg B.W.), (e) TF-60 (60 mg/kg B.W.), and (f) TF-100 (100 mg/kg B.W.). OA was induced by an intra-articular injection of 3 mg MIA into the right hind knee joint. The animals received either Celecoxib or TF through oral gavage over 28 days. The vehicle control animals received intra-articular sterile normal saline. Results: Post-treatment, NXT15906F6 groups showed significant (p < 0.05) dose- dependent pain relief as evidenced by improved body weight-bearing capacity on the right hind limb. NXT15906F6 treatment also significantly reduced the serum tumor necrosis factor-a (TNF-alpha, p < 0.05) and nitrite (p < 0.05) levels in a dose-dependent manner. mRNA expression analyses revealed the up-regulation of collagen type-II (COL2A1) and down-regulation of matrix metalloproteinases (MMP-3, MMP-9 and MMP-13) in the cartilage tissues of NXT15906F6-supplemented rats. Cyclooxygenase-2 and inducible nitric oxide synthase (iNOS) protein expressions were down-regulated. Decreased immunolocalization of NF-kappa ss (p65) was observed in the joint tissues of NXT15906F6-supplemented rats. Furthermore, microscopic observations revealed that NXT15906F6 preserved MIA-induced rats' joint architecture and integrity. Conclusion: NXT15906F6 reduces MIA-induced joint pain, inflammation, and cartilage degradation in rats.
引用
收藏
页码:48 / 58
页数:11
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