Vasil'eva T M, Makarov V A, Petrukhina G N, Voiushina T L, Iusupova M P, Novgorodova S A, Kotlova E K
Eksp Klin Farmakol. 2006 Jul-Aug;69(4):39-42.
The influence of new synthetic peptides ARGDS-NH2 and RGD-dFK (synthesized by the fermentative method) and VPNLRGDLQVLA (a fragment of the foot-and-mouth virus's surface peptide) on the ADP-induced human platelet aggregation in vitro was studied. All peptides were found to inhibit the human platelet aggregation, but the synthetic peptides (ARGDS-NH2 and RGD-dFK) showed the most pronounced effect. Significant decrease in the platelet aggregation was observed at their concentrations within 0.1-10 mM. ARGDS-NH2 and RGD-dFK inhibited the platelet aggregation stronger than the reference drug pentoxifylline at equivalent concentrations.
研究了新型合成肽ARGDS-NH2和RGD-dFK(通过发酵法合成)以及VPNLRGDLQVLA(口蹄疫病毒表面肽的一个片段)对体外ADP诱导的人血小板聚集的影响。发现所有肽均能抑制人血小板聚集,但合成肽(ARGDS-NH2和RGD-dFK)表现出最显著的效果。在其浓度为0.1 - 10 mM时,观察到血小板聚集显著降低。在等效浓度下,ARGDS-NH2和RGD-dFK比参比药物己酮可可碱更能抑制血小板聚集。