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HerbalSiam Superstore of Herbs and Remedies
Shipping Worldwide since 2001. Bangkok, Thailand.
Garcinia Cambodia
Pien Tze Huang. Original
Krachai Dam Black Ginger
Xiao Feng Tang : Psoriasis
Jiu Jeng Pushen Jiao Nang
Curcuma Longa Turmeric 100 caps
Bitter Gourd - Momordica
Si Wu Tang - Tonic Tea for Anemia. Excellent
American Ginseng Instant Tea
Yindan Ping Gan Capsules
Juan Bi Tang - Arthritis remedy
Butea Superba
Pueraria Mirifica
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Kochia Coparia (L) Schrad
Price:
$1.00
Latin Name:
Kochia scoparia (L.) Schrad.
PinYin Name:
difuzi Ethnopharmacological relevance: Fuzi is an effective but toxic traditional Chinese medicine (TCM) derived from Aconitum carmichaeli. In our previous study, detoxicated Fuzi (d-Fuzi) has been originally developed with no toxicity but significant efficacy. However, whether d-Fuzi can be used for therapy of osteoarthritis (OA), remain unknown.Materials and methods: Severe OA model was established by intra-articular mono-iodoacetate (MIA) injection (1.25mg) into rats and orally treated with 2g/ml d-Fuzi at a dosage of 7ml/kg body weight for 28 days. In vivo, the articular radiographic and histopathologic analyses were performed to qualitatively assess the chondroprotective effect of d-Fuzi, followed by quantitative measurements of bone density and Mankin scores. In vitro, such effect on chondrocyte viability after MIA attack was evaluated. Hybrid quadrupole time-of-flight mass spectrometry (QTOF-MS) was performed for chemical analysis of d-Fuzi.Results: d-Fuzi was demonstrated to possess chondroprotective activity on MIA-induced OA model by in vivo preventing the articular degeneration and the reducing of bone density and Mankin score, as well as by in vitro promoting the chondrocyte proliferation and inhibiting the MIA-induced chondrocyte damage. A total of 23 compounds were identified in d-Fuzi, most of which were deduced as the non-toxic derivatives of aconite alkaloids.Conclusions: This is the first report regarding chondroprotective effect and chemical profile of d-Fuzi, originally revealing its great anti-OA potential and thereby providing a promising TCM candidate for OA therapy.
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