Kazama Y, Niwa M, Yamagishi R, Takahashi K, Sakuragawa N, Koide T
Central Clinical Laboratory, Toyama Medical and Pharmaceutical University, Japan.
Thromb Res. 1987 Oct 15;48(2):179-85. doi: 10.1016/0049-3848(87)90414-2.
The ability of various sulfated polysaccharides to activate protein C inhibitor (PCI) and the effect of molecular weight (Mr) and sulfur content of dextran sulfates were investigated. Besides dextran sulfate, highly sulfated polysaccharides such as chondroitin polysulfates 1 and 5, and pentosan polysulfate were more active than heparin in enhancing the activated protein C inhibition by PCI. The molecular weight and the sulfur content of dextran sulfate were critical for the second-order rate constant of the reaction and for the optimal concentration of the polysaccharide, respectively. These results suggest that the carboxyl groups of polysaccharides are not necessarily required, but some sulfate groups within polymers may play a critical role in the interaction with PCI.
研究了各种硫酸化多糖激活蛋白C抑制剂(PCI)的能力以及硫酸葡聚糖的分子量(Mr)和硫含量的影响。除了硫酸葡聚糖外,高度硫酸化的多糖如硫酸软骨素1和5以及戊聚糖硫酸酯在增强PCI对活化蛋白C的抑制作用方面比肝素更具活性。硫酸葡聚糖的分子量和硫含量分别对反应的二级速率常数和多糖的最佳浓度至关重要。这些结果表明,多糖的羧基不一定是必需的,但聚合物中的一些硫酸根基团可能在与PCI的相互作用中起关键作用。