Department of Orthopaedic Surgery, Nihon University School of Medicine, 30-1, Ohyaguchikami-cho, Itabashi-ku, Tokyo 173-8610, Japan.
J Orthop Res. 2012 May;30(5):673-8. doi: 10.1002/jor.22003. Epub 2011 Nov 4.
Histological and molecular changes were examined to investigate the effects of long-term administration of glucosamine (GlcN) and chondroitin sulfate (CS) in a model of spontaneous osteoarthritis (OA) in Hartley guinea pigs. Three groups of female 3-week-old Hartley guinea pigs received GlcN, CS, and neither agent, respectively. Five animals in each group were sacrificed at 8, 12, and 18 months of age. At 8 months of age, Hartley guinea pigs had severe degeneration of knee joint cartilage, chondrocyte apoptosis, marked reduction of tissue total RNA, decreases of aggrecan and collagen type 2 mRNAs, and increases in MMP-3 and MMP-8 mRNAs. Long-term administration of GlcN and CS reduced cartilage degeneration at 8 months of age. The marked loss of total RNA and the increase in MMP-3 mRNA were also inhibited by GlcN and CS. Thus, long-term oral administration of GlcN or CS inhibits OA progression, maintains total RNA and down-regulates MMP-3 mRNA in a spontaneous OA model in Hartley guinea pigs.
为了研究氨基葡萄糖(GlcN)和硫酸软骨素(CS)长期给药对自发性骨关节炎(OA)模型的影响,我们观察了组织学和分子变化。三组 3 周龄雌性 Hartley 豚鼠分别给予 GlcN、CS 和两者均不给药。每组各有 5 只动物分别在 8、12 和 18 个月时处死。8 个月时,Hartley 豚鼠膝关节软骨严重退变,软骨细胞凋亡,组织总 RNA 明显减少,聚集蛋白聚糖和 II 型胶原 mRNA 减少,MMP-3 和 MMP-8 mRNA 增加。GlcN 和 CS 的长期给药可减轻 8 个月时的软骨退变。GlcN 和 CS 还抑制了总 RNA 的明显丢失和 MMP-3 mRNA 的增加。因此,长期口服 GlcN 或 CS 可抑制 Hartley 豚鼠自发性 OA 模型中 OA 的进展,维持总 RNA 并下调 MMP-3 mRNA。
Front Aging. 2021-9-8
World J Orthop. 2017-1-18
Arthritis Res Ther. 2015-9-14
Curr Rheumatol Rep. 2013-10
Arthritis Rheum. 2013-7