Abstract
The dermatan sulfate (DS) isolated from the ray skin Raja montagui was identified and characterized. Its average molecular weight (Mw) and sulfate content were 39kDa and 25% w/w, respectively. This DS prolonged thrombin time and activated partial thromboplastin time and inhibited the thrombin generation in a concentration-dependent manner whereas it had no effect on the anti-Xa assay and on platelet function. Data from the anti-IIa assay allowed the assessment of the specific anticoagulant activity which was 40units/mg. The kinetics of the thrombin inhibition by heparin cofactor II (HCII) has been studied as a function of DS concentration according to a kinetic model in which the polysaccharide binds quickly to the inhibitor and forms a complex more reactive than the free inhibitor towards thrombin. This DS accelerated thrombin inhibition exclusively by HCII. The dissociation constant of the DS-HCII complex, KDSHCII, and the rate constant of the thrombin inhibition by this complex, k, were (2.93±0.25)×10-6M and (2.2±0.35)×109M-1min-1, respectively.Our findings indicated that the major polysaccharide in the skin of the ray Raja montagui was a DS endowed with a high anticoagulant effect mediated by HCII and which may constitute an anticoagulant drug of interest in anticoagulant therapy. © 2010 Elsevier Inc.
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Mansour, M. B., Dhahri, M., Hassine, M., Ajzenberg, N., Venisse, L., Ollivier, V., … Maaroufi, R. M. (2010). Highly sulfated dermatan sulfate from the skin of the ray Raja montagui: anticoagulant activity and mechanism of action. Comparative Biochemistry and Physiology - B Biochemistry and Molecular Biology, 156(3), 206–215. https://doi.org/10.1016/j.cbpb.2010.03.010
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