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Metabolic Regulatory and Anti-oxidative Effects of Modified Bushen Huoxue Decoction(补肾活血方) on Experimental Rabbit Model of Osteoarthritis 被引量:17

Metabolic Regulatory and Anti-oxidative Effects of Modified Bushen Huoxue Decoction(补肾活血方) on Experimental Rabbit Model of Osteoarthritis
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摘要 Objective: To observe the metabolic, regulatory and anti-oxidative effects of modified Bushen Huoxue Decoction (BSHXD, 补肾活血方), a Chinese herbal medicine for Kidney (Shen)-reinforcement and bloodactivation, on an osteoarthritis (OA) rabbit model. Methods: A rabbit model for knee joint OA was established by the classic Huith's method. The OA model rabbits were randomized into 5 groups: the model control group, the positive control group treated with glucosamine sulfate, and the three BSHXD treated groups treated respectively with low, moderate, and high doses of BSHXD. In addition, a normal control group and a sham-operated group were set up. Experimental animals were sacrificed after a 7-week treatment, and pathological changes in cartilaginous tissue were estimated using the Mankin criteria. Hydroxyproline (Hyp) and malonaldehyde (MDA) contents in blood serum and urine, as well as superoxide dismutase (SOD) activity and nitric oxide (NO) content in blood serum and knee joint synovial homogenates were detected. Results: Mankin scoring showed insignificant statistical differences between the various treatment groups (P〉0.05), but all were better than the model control group (P〈0.05). Serum and udnary contents of Hyp and MDA as well as serum and synovial levels of NO were significantly lower, but the SOD activity in blood serum and synovial tissue was higher in the BSHXD treated groups than in the model group (P〈0.01); the effect of BSHXD was dose-dependent to some extent. Coaclasloa: The modified BSHXD shows an effect of improving cartilage metabolism in experimental rabbits with OA, and possesses osteo-chondric protective effects in antagonizing peroxidation injury. Objective: To observe the metabolic, regulatory and anti-oxidative effects of modified Bushen Huoxue Decoction (BSHXD, 补肾活血方), a Chinese herbal medicine for Kidney (Shen)-reinforcement and bloodactivation, on an osteoarthritis (OA) rabbit model. Methods: A rabbit model for knee joint OA was established by the classic Huith's method. The OA model rabbits were randomized into 5 groups: the model control group, the positive control group treated with glucosamine sulfate, and the three BSHXD treated groups treated respectively with low, moderate, and high doses of BSHXD. In addition, a normal control group and a sham-operated group were set up. Experimental animals were sacrificed after a 7-week treatment, and pathological changes in cartilaginous tissue were estimated using the Mankin criteria. Hydroxyproline (Hyp) and malonaldehyde (MDA) contents in blood serum and urine, as well as superoxide dismutase (SOD) activity and nitric oxide (NO) content in blood serum and knee joint synovial homogenates were detected. Results: Mankin scoring showed insignificant statistical differences between the various treatment groups (P〉0.05), but all were better than the model control group (P〈0.05). Serum and udnary contents of Hyp and MDA as well as serum and synovial levels of NO were significantly lower, but the SOD activity in blood serum and synovial tissue was higher in the BSHXD treated groups than in the model group (P〈0.01); the effect of BSHXD was dose-dependent to some extent. Coaclasloa: The modified BSHXD shows an effect of improving cartilage metabolism in experimental rabbits with OA, and possesses osteo-chondric protective effects in antagonizing peroxidation injury.
出处 《Chinese Journal of Integrative Medicine》 SCIE CAS 2013年第6期459-463,共5页 中国结合医学杂志(英文版)
基金 Supported by Practice Basic Research Plan of Tianjin City(No. 06YFJMJC09600)
关键词 Kidney-reinforcing and blood-activating OSTEOARTHRITIS HYDROXYPROLINE MALONALDEHYDE superoxide dismutase nitric oxide Kidney-reinforcing and blood-activating osteoarthritis hydroxyproline malonaldehyde superoxide dismutase nitric oxide
作者简介 Correspondence to: Dr. WU Yuan-hao, Tel: 86-22-27432720, E-mail: doctor.wuyh @ gmail.com
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