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Open AccessJournal ArticleDOI

Effect of GCSB-5, a Herbal Formulation, on Monosodium Iodoacetate-Induced Osteoarthritis in Rats.

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TLDR
Results indicate that GCSB-5 is a potential therapeutic agent for the protection of articular cartilage against progression of osteoarthritis through inhibition of MMPs activity, inflammatory mediators, and NF-κB activation.
Abstract
Therapeutic effects of GCSB-5 on osteoarthritis were measured by the amount of glycosaminoglycan in rabbit articular cartilage explants in vitro, in experimental osteoarthritis induced by intra-articular injection of monoiodoacetate in rats in vivo. GCSB-5 was orally administered for 28 days. In vitro, GCSB-5 inhibited proteoglycan degradation. GCSB-5 significantly suppressed the histological changes in monoiodoacetate-induced osteoarthritis. Matrix metalloproteinase (MMP) activity, as well as, the levels of serum tumor necrosis factor-α, cyclooxygenase-2, inducible nitric oxide synthase protein, and mRNA expressions were attenuated by GCSB-5, whereas the level of interleukin-10 was potentiated. By GCSB-5, the level of nuclear factor-κB p65 protein expression was significantly attenuated but, on the other hand, the level of inhibitor of κB-α protein expression was increased. These results indicate that GCSB-5 is a potential therapeutic agent for the protection of articular cartilage against progression of osteoarthritis through inhibition of MMPs activity, inflammatory mediators, and NF-κB activation.

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Stimulation of cytokine and chemokine expression by human articular chondrocytes in response to fibronectin fragments

J Pulai
TL;DR: In this article, the authors used a 110kD FN-f (0.5-1µM) to stimulate chondrocyte expression of the pro-inflammatory cytokines IL-1, IL-6, IL -8, MCP-1 and GRO-s.
Journal ArticleDOI

Coupling Freshly Isolated CD44+ Infrapatellar Fat Pad‐Derived Stromal Cells with a TGF‐β3 Eluting Cartilage ECM‐Derived Scaffold as a Single‐Stage Strategy for Promoting Chondrogenesis

TL;DR: A cartilage extracellular matrix (ECM)‐derived scaffold that could facilitate the rapid proliferation and chondrogenic differentiation of freshly isolated stromal cells is developed and opens up new possibilities for in‐theatre cell‐based therapies for joint regeneration.
Journal ArticleDOI

Usage report of pharmacopuncture in musculoskeletal patients visiting Korean medicine hospitals and clinics in Korea.

TL;DR: Patterns of pharmacopuncture use for musculoskeletal disease treatment in Korea are verified, and use of Pharmacopuncture varied depending on disease or symptom severity, which is expected to contribute to future clinical study design and standardization.
Journal ArticleDOI

Effects of intra-articular SHINBARO treatment on monosodium iodoacetate-induced osteoarthritis in rats

TL;DR: Intra-articular administration of SHINBARO (IAS) at 20 mg/kg remarkably restrained the decrease in bone volume/total volume and modulated the balance of inflammatory enzymes, mediators, and cytokines in the MIA-induced osteoarthritis rat model.
References
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Journal ArticleDOI

Interleukin-10 and the interleukin-10 receptor.

TL;DR: Findings that have advanced the understanding of IL-10 and its receptor are highlighted, as well as its in vivo function in health and disease.
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Series Introduction: The transcription factor NF-κB and human disease

TL;DR: It is shown that the transcription factor NF-κB has been shown to be the target of several anti-inflammatory and anticancer drugs.
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The matrix metalloproteinases and their inhibitors.

TL;DR: A number of metalloproteinases that degrade the extracellular matrix of connective tissues and two specific tissue inhibitors of met ALLPs have now been isolated, characterized, and cloned, and initial studies have been carried out to assess the contribution to their biochemical and biologic properties.
Journal ArticleDOI

Weight bearing as a measure of disease progression and efficacy of anti-inflammatory compounds in a model of monosodium iodoacetate-induced osteoarthritis

TL;DR: The determination of differences in hind paw weight distribution in the rat MIA model of OA is a technically straightforward, reproducible method that is predictive of the effects of anti-inflammatory and analgesic agents and useful for the discovery of novel pharmacologic agents in human OA.
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