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口服氨基葡萄糖对兔骨关节炎模型软骨降解的影响。

Effect of oral glucosamine on cartilage degradation in a rabbit model of osteoarthritis.

作者信息

Tiraloche Gabrielle, Girard Christiane, Chouinard Luc, Sampalis John, Moquin Luc, Ionescu Mirela, Reiner Agnes, Poole A Robin, Laverty Sheila

机构信息

Faculté de Médecine Vétérinaire, Université de Montréal, St. Hyacinthe, Quebec, Canada.

出版信息

Arthritis Rheum. 2005 Apr;52(4):1118-28. doi: 10.1002/art.20951.

Abstract

OBJECTIVE

To determine whether oral glucosamine alleviates cartilage degradation in an animal model of osteoarthritis (OA).

METHODS

The effect of 8 weeks of daily oral glucosamine hydrochloride on degeneration of articular cartilage was evaluated in rabbits in which anterior cruciate ligament transection (ACLT) was performed to induce OA. Animals were treated with glucosamine (n = 16) or a placebo (n = 16) and necropsied at 11 weeks. Seven unoperated rabbits served as controls. The articular cartilage was evaluated macroscopically and histologically and analyzed for total type II collagen and glycosaminoglycan (GAG) content.

RESULTS

Histologic analysis revealed that loss of proteoglycan, based on Safranin O-fast green staining, was significantly reduced in the lateral tibial plateau cartilage of ACL-transected limbs in the glucosamine group compared with ACL-transected limbs in the placebo group, with a similar, but not significant, trend for the lateral femoral condylar cartilage. Likewise, macroscopic analysis of cartilage showed that the lateral tibial plateau alone had a significantly lower rate of disease in the glucosamine group, which was consistent with the results of the independent histologic assessment. However, no significant treatment effect was detected when composite histologic scores were analyzed. A significant reduction in GAG content was observed in the femoral condyles of placebo-treated ACL-transected joints, but not in the same region of glucosamine-treated ACL-transected joints, compared with their respective contralateral unoperated joints.

CONCLUSION

Oral administration of glucosamine had a detectable, site-specific, partial disease-modifying effect in this model of OA. From a clinical perspective, the administration of glucosamine did not prevent fibrillation and/or erosions of the articular cartilage in all of the treated animals, and no effects were detected in the medial joint compartments.

摘要

目的

确定口服氨基葡萄糖是否能减轻骨关节炎(OA)动物模型中的软骨退变。

方法

在通过切断前交叉韧带(ACLT)诱导OA的兔子中,评估每日口服盐酸氨基葡萄糖8周对关节软骨退变的影响。将动物分为氨基葡萄糖组(n = 16)或安慰剂组(n = 16),并在11周时进行尸检。7只未手术的兔子作为对照。对关节软骨进行宏观和组织学评估,并分析其II型胶原蛋白和糖胺聚糖(GAG)的总含量。

结果

组织学分析显示,与安慰剂组的ACL切断肢体相比,氨基葡萄糖组中ACL切断肢体的胫骨外侧平台软骨中,基于番红O-固绿染色的蛋白聚糖损失显著减少,股骨外侧髁软骨也有类似但不显著的趋势。同样,软骨的宏观分析表明,仅胫骨外侧平台在氨基葡萄糖组中的疾病发生率显著较低,这与独立组织学评估的结果一致。然而,分析综合组织学评分时未检测到显著的治疗效果。与各自对侧未手术关节相比,安慰剂治疗的ACL切断关节的股骨髁中GAG含量显著降低,但氨基葡萄糖治疗的ACL切断关节的相同区域未出现这种情况。

结论

在该OA模型中,口服氨基葡萄糖具有可检测到的、位点特异性的、部分疾病修饰作用。从临床角度来看,氨基葡萄糖给药并不能防止所有治疗动物的关节软骨发生纤维化和/或糜烂,并且在内侧关节腔中未检测到效果。

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