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
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
相关论文
共 13 条
  • [1] A Combination of Tamarindus indica seeds and Curcuma longa Rhizome Extracts Improves Knee Joint Function and Alleviates Pain in Non-Arthritic Adults Following Physical Activity
    Rao, Posani Sriruivas
    Ramanjaneyulu, Yendluri Sita
    Prisk, Victor R.
    Schurgers, Leon J.
    INTERNATIONAL JOURNAL OF MEDICAL SCIENCES, 2019, 16 (06): : 845 - 853
  • [2] Resveratrol, a natural antioxidant, protects monosodium iodoacetate-induced osteoarthritic pain in rats
    Wang, Zhu-Min
    Chen, Yong-Cai
    Wang, Da-Peng
    BIOMEDICINE & PHARMACOTHERAPY, 2016, 83 : 763 - 770
  • [3] The effects of intra-articular resiniferatoxin on monosodium iodoacetate-induced osteoarthritic pain in rats
    Kim, Youngkyung
    Kim, Eun-hye
    Lee, Kyu Sang
    Lee, Koeun
    Park, Sung Ho
    Na, Sook Hyun
    Ko, Cheolwoong
    Kim, Junesun
    Yooon, Young Wook
    KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY, 2016, 20 (01): : 129 - 136
  • [4] Reduction of SIRT1 Mediates Monosodium Iodoacetate-Induced Osteoarthritic Pain by Upregulating p53 Expression in Rats
    Xu, Ling-Jun
    Liu, Cui-Cui
    Chen, Lu-Miao
    Wu, Gui-Hao
    Wang, Xiao-Ping
    PAIN PHYSICIAN, 2021, 24 (07) : E1025 - E1034
  • [5] Agkistrodon ameliorates pain response and prevents cartilage degradation in monosodium iodoacetate-induced osteoarthritic rats by inhibiting chondrocyte hypertrophy and apoptosis
    Wang, Caiwei
    Yan, Li
    Yan, Bo
    Zhou, Li
    Sun, Wan
    Yu, Lingying
    Liu, Fucun
    Du, Wenxi
    Yu, Guangping
    Hu, Zhengyan
    Yuan, Qiang
    Xiao, Luwei
    Li, Hongwen
    Tong, Peijian
    Zhang, Jida
    Shan, Letian
    Efferth, Thomas
    JOURNAL OF ETHNOPHARMACOLOGY, 2019, 231 : 545 - 554
  • [6] Krill Oil Attenuates Inflammation in Monosodium Iodoacetate-Induced Osteoarthritic Rats, SW982 Synovial Cell Line, and Primary Chondrocytes
    Kim, Ok-Kyung
    Kim, Dakyung
    Lee, Minhee
    Park, Seong-Hoo
    Jung, Jaeeun
    Lee, Jeongmin
    JOURNAL OF MEDICINAL FOOD, 2022, 25 (03) : 239 - 250
  • [7] UP1304, a Botanical Composition Containing Two Standardized Extracts of Curcuma longa and Morus alba, Mitigates Pain and Inflammation in Adjuvant-induced Arthritic Rats
    Yimam, Mesfin
    Lee, Young-Chul
    Moore, Breanna
    Jiao, Ping
    Hong, Mei
    Nam, Jeong-Bum
    Kim, Mi-Ran
    Kim, Tae-Woo
    Kim, Hyun-Jin
    Hyun, Eu-Jin
    Chu, Min
    Brownell, Lidia
    Jia, Qi
    PHARMACOGNOSY RESEARCH, 2016, 8 (02): : 112 - 117
  • [8] Monosodium iodoacetate-induced inflammation and joint pain are reduced in TRPA1 deficient mice - potential role of TRPA1 in osteoarthritis
    Moilanen, L. J.
    Hamalainen, M.
    Nummenmaa, E.
    Ilmarinen, P.
    Vuolteenaho, K.
    Nieminen, R. M.
    Lehtimaki, L.
    Moilanen, E.
    OSTEOARTHRITIS AND CARTILAGE, 2015, 23 (11) : 2017 - 2026
  • [9] Transient receptor potential ankyrin-1 (TRPA1) as a novel factor in osteoarthritis: TRPA1 ion channel mediates monosodium iodoacetate (MIA)-induced acute inflammation and contributes to the development of cartilage degradation and joint pain in the MIA model of osteoarthritis
    Moilanen, L. J.
    Hamalainen, M.
    Nummenmaa, E.
    Ilmarinen, P.
    Vuolteenaho, K.
    Nieminen, R.
    Lehtimaki, L.
    Moilanen, E.
    SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 2018, 47 : 10 - 10
  • [10] Soluble CCR2 gene therapy controls joint inflammation, cartilage damage, and the progression of osteoarthritis by targeting MCP-1 in a monosodium iodoacetate (MIA)-induced OA rat model
    Hyun Sik Na
    Seon-Yeong Lee
    Dong Hwan Lee
    Jin Seok Woo
    Si-Young Choi
    Keun-Hyung Cho
    Seon Ae Kim
    Eun Jeong Go
    A Ram Lee
    Jeong-Won Choi
    Seok Jung Kim
    Mi-La Cho
    Journal of Translational Medicine, 20