SYNERGISTIC INHIBITION OF PLATELET-AGGREGATION BY FIBRINOGEN-RELATED PEPTIDES

被引:18
作者
ADELMAN, B
GENNINGS, C
STRONY, J
HANNERS, E
机构
[1] VIRGINIA COMMONWEALTH UNIV,MED COLL VIRGINIA,DEPT MED,RICHMOND,VA 23298
[2] VIRGINIA COMMONWEALTH UNIV,MED COLL VIRGINIA,DEPT BIOSTAT,RICHMOND,VA 23298
[3] VET AFFAIRS MED CTR,HUNTER HOLMES MCGUIRE DEPT,RICHMOND,VA
关键词
Blood platelets; Fibrinogen; Peptides; Thrombosis; Von Willebrand factor;
D O I
10.1161/01.RES.67.4.941
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have evaluated the ability of the fibrinogen-related peptides Gly-Arg-Gly-Asp-Ser (GRGDS), Gly-Gln-Gln-His-His-Leu-Gly-Gly-Ala-Lys-Gln-Ala-Gly-Asp-Val (γ-chain peptide), and Gly-Pro-Arg-Pro (GPRP) to inhibit platelet aggregation in platelet-rich plasma individually and in combination. When used alone, GRGDS totally inhibited ADP-induced aggregation of human platelets in platelet-rich plasma; however, the maximum inhibitory effect of the other peptides was less than 80%. The concentrations necessary to inhibit platelet aggregation in plasma by 50% were 100 μmol/l and 1 and 3.2 mmol/l for GRGDS, γ-chain peptide, and GPRP, respectively. When evaluating the effect of peptide mixtures, we discovered that the combination GPRP + GRGDS worked together synergistically (p < 0.001, analysis by surface response methodology), whereas GPRP + γ-chain peptide did not. For example, our analysis indicated that a mixture of 50 μmol/l GRGDS plus 180 μmol/l GPRP would produce 50% inhibition of platelet aggregation. This is an effect twofold greater than that produced by 50 μmol/l GRGDS alone, and one that would require an 18-fold greater concentration of GPRP if used alone. These data indicate that the combination GPRP + GRGDS inhibited platelet aggregation in plasma in a synergistic fashion and suggest the potential value of their combined use in antithrombotic therapy.
引用
收藏
页码:941 / 947
页数:7
相关论文
共 37 条
[1]  
ADELMAN B, 1987, BLOOD, V70, P1362
[2]  
ANDRIEUX A, 1989, J BIOL CHEM, V264, P9258
[3]  
[Anonymous], 1989, NEW ENGL J MED, V321, P129
[4]   PREVENTION OF OCCLUSIVE CORONARY-ARTERY THROMBOSIS BY A MURINE MONOCLONAL-ANTIBODY TO PORCINE VONWILLEBRAND-FACTOR [J].
BELLINGER, DA ;
NICHOLS, TC ;
READ, MS ;
REDDICK, RL ;
LAMB, MA ;
BRINKHOUS, KM ;
EVATT, BL ;
GRIGGS, TR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (22) :8100-8104
[5]  
BENNETT JS, 1988, J BIOL CHEM, V263, P12948
[6]   CRITERIA FOR ANALYZING INTERACTIONS BETWEEN BIOLOGICALLY-ACTIVE AGENTS [J].
BERENBAUM, MC .
ADVANCES IN CANCER RESEARCH, 1981, 35 :269-335
[7]  
CARCHMAN RA, 1989, ANTIEPILEPTIC DRUG I, P245
[8]   PLATELET GLYCOPROTEIN-IIB AND GLYCOPROTEIN-IIIA - EVIDENCE FOR A FAMILY OF IMMUNOLOGICALLY AND STRUCTURALLY RELATED GLYCOPROTEINS IN MAMMALIAN-CELLS [J].
CHARO, IF ;
FITZGERALD, LA ;
STEINER, B ;
RALL, SC ;
BEKEART, LS ;
PHILLIPS, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (21) :8351-8355
[9]   RECOGNITION OF DISTINCT ADHESIVE SITES ON FIBRINOGEN BY RELATED INTEGRINS ON PLATELETS AND ENDOTHELIAL-CELLS [J].
CHERESH, DA ;
BERLINER, SA ;
VICENTE, V ;
RUGGERI, ZM .
CELL, 1989, 58 (05) :945-953
[10]  
CLAUSS A., 1957, ACTA HAEMATOL, V17, P237