Intra-Articular Delivery of Glucosamine for Treatment of Experimental Osteoarthritis Created by a Medial Meniscectomy in a Rat Model

被引:21
|
作者
Gibson, Matthew [1 ,2 ]
Li, Hanwei [1 ,2 ]
Coburn, Jeannine [3 ]
Moroni, Lorenzo [1 ,2 ]
Nahas, Zayna [1 ,2 ]
Bingham, Clifford, III [4 ]
Yarema, Kevin [1 ,2 ]
Elisseeff, Jennifer [1 ,2 ]
机构
[1] Wilmer Eye Inst, Translat Tissue Engn Ctr, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21287 USA
[4] Johns Hopkins Univ, Div Rheumatol, Dept Med, Baltimore, MD 21224 USA
基金
美国国家卫生研究院;
关键词
glucosamine; osteoarthritis; rat arthritis; animal models; MESENCHYMAL STEM-CELLS; CHONDROITIN SULFATE; ARTICULAR CHONDROCYTES; KNEE OSTEOARTHRITIS; GENE-EXPRESSION; BASIC SCIENCE; IN-VITRO; CARTILAGE; MATRIX; BONE;
D O I
10.1002/jor.22445
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Glucosamine (GlcN) is a naturally occurring amino-monosaccharide with putative chondroprotective activity. Optimum responses to GlcN are achieved at concentrations which are impractical with oral dosing. Intra-articular delivery of a bolus dose of GlcN is one way to overcome these pharmacokinetic obstacles. In this study we report the effects of exposing primary human chondrocytes to a bolus dose of GlcN. We also locally administered GlcN in the context of a meniscal transection model of rat osteoarthritis (OA). The knees of male rats were subjected to medial meniscal transection and developed arthritic changes over 4 weeks. Treatment groups were then given thrice weekly 100L injections of 35g, 350g, 1.8mg, or 3.5mg of GlcN dissolved in normal saline. Gross images, modified Mankin scores, and histomorphometric measurements were used as outcome measures. The 350g dosage of GlcN had the most significant positive impact on all components of the modified Mankin score. Together, these findings suggest the local delivery of high concentrations of GlcN is well tolerated and can suppress experimental OA through influences on both bone and cartilage. (c) 2013 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 32:302-309, 2014.
引用
收藏
页码:302 / 309
页数:8
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