Qu Cheng-Juan, Karjalainen Hannu M, Helminen Heikki J, Lammi Mikko J
Department of Anatomy, Institute of Biomedicine, University of Kuopio, PO Box 1627, 70211 Kuopio, Finland.
Biochim Biophys Acta. 2006 Apr;1762(4):453-9. doi: 10.1016/j.bbadis.2006.01.005. Epub 2006 Feb 10.
Glucosamine and glucosamine sulphate have been promoted as a disease-modifying agent to improve the clinical symptoms of osteoarthritis. The precise mechanism of the action of the suggested positive effect of glucosamine or glucosamine sulphate on cartilage proteoglycans is not known, since the level of glucosamine in plasma remains very low after oral administration of glucosamine sulphate. We examined whether exogenous hexosamines or their sulphated forms would increase steady-state levels of aggrecan and hyaluronan synthase (HAS) or glycosaminoglycan synthesis using Northern blot and (35)S-sulphate incorporation analyses. Total RNA was extracted from bovine primary chondrocytes which were cultured either in 1 mM concentration of glucosamine, galactosamine, mannosamine, glucosamine 3-sulphate, glucosamine 6-sulphate or galactosamine 6-sulphate for 0, 4, 8 and 24 h, or in three different concentrations (control, 100 microM and 1 mM) of glucosamine sulphate salt or glucose for 24 or 72 h. Northern blot assay showed that neither hexosamines nor glucosamine sulphate salt stimulated aggrecan and HAS-2 mRNA expression. Glycosaminoglycan synthesis remained at a control level in the treated cultures, with the exception of mannosamine which inhibited (35)S-sulphate incorporation in low-glucose DMEM treatment. In our culture conditions, hexosamines or their sulphated forms did not increase aggrecan expression or (35)S-sulphate incorporation.
氨基葡萄糖和硫酸氨基葡萄糖已被推广为一种改善骨关节炎临床症状的病情缓解剂。氨基葡萄糖或硫酸氨基葡萄糖对软骨蛋白聚糖产生预期积极作用的确切作用机制尚不清楚,因为口服硫酸氨基葡萄糖后血浆中的氨基葡萄糖水平仍然很低。我们使用Northern印迹法和(35)S-硫酸盐掺入分析,研究了外源性己糖胺或其硫酸化形式是否会增加聚集蛋白聚糖和透明质酸合酶(HAS)的稳态水平或糖胺聚糖的合成。从牛原代软骨细胞中提取总RNA,这些细胞分别在1 mM浓度的氨基葡萄糖、半乳糖胺、甘露糖胺、3-硫酸氨基葡萄糖、6-硫酸氨基葡萄糖或6-硫酸半乳糖胺中培养0、4、8和24小时,或者在三种不同浓度(对照、100 microM和1 mM)的硫酸氨基葡萄糖盐或葡萄糖中培养24或72小时。Northern印迹分析表明,己糖胺和硫酸氨基葡萄糖盐均未刺激聚集蛋白聚糖和HAS-2 mRNA的表达。除了甘露糖胺在低糖DMEM处理中抑制(35)S-硫酸盐掺入外,处理后的培养物中糖胺聚糖的合成保持在对照水平。在我们的培养条件下,己糖胺或其硫酸化形式不会增加聚集蛋白聚糖的表达或(35)S-硫酸盐掺入。
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