In vitro and in vivo anti-platelet effects of enzymatic hydrolysates of collagen and collagen-related peptides

被引:18
作者
Nonaka, I
Katsuda, SI
Ohmori, T
Shigehisa, T
Nakagami, T
Maruyama, S
机构
[1] NIPPON MEAT PACKERS INC, CTR RES & DEV, DEPT HLTH & DIETARY SCI, TSUKUBA, IBARAKI 30026, JAPAN
[2] NATL INST BIOSCI & HUMAN TECHNOL, AGCY IND SCI & TECHNOL, TSUKUBA, IBARAKI 305, JAPAN
关键词
collagen; collagenase; collagen-related synthetic peptide; fibrinogen; thrombin;
D O I
10.1271/bbb.61.772
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Collagen-related peptides, Gly-Pro-Arg and its analogues,, were examined for their inhibitory effects on platelet aggregation induced by the addition of ADP. Human platelet aggregation was suppressed by more than 50% with each of Gly-Pro-Arg and such Gly-Pro-Arg-containing peptides as Gly-Pro-Arg-Gly, Gly-Pro-Arg-Gly-Pro, Gly-Pro-Arg-Pro-Pro, and Gly-Pro-Arg-Pro-Pro-Pro at a concentration of 0.3 mar. The inhibitory effects of these peptides were about 10 times higher in human PRP than in rat PRP, Other Gly-Pro-Arg analogues such as Sar-Pro-Arg, Gly-Pro-Lys, Gly-Ala-Arg, and Ala-Gly-Pro-Arg had no inhibitory effect at a concentration from 0.1 to 0.8 mM even in human PRP. Intravenous and oral administrations of Gly-Pro-Arg and enzymatic hydrolysates of collagen suppressed the decrease in platelet count for endotoxin-induced DIC in rats, Collagen itself has been regarded as a potent inducer of platelet aggregation, but these findings suggest that collagen-related peptides and enzymatic hydrolysates of collagen prevent platelet aggregation.
引用
收藏
页码:772 / 775
页数:4
相关论文
共 22 条
[1]   COLLAGEN DERIVED OCTAPEPTIDE INHIBITS PLATELET PROCOAGULANT ACTIVITY INDUCED BY THE COMBINED ACTION OF COLLAGEN AND THROMBIN [J].
BEVERS, EM ;
KARNIGUIAN, A ;
LEGRAND, YJ ;
ZWAAL, RFA .
THROMBOSIS RESEARCH, 1985, 37 (03) :365-370
[2]   AGGREGATION OF BLOOD PLATELETS BY ADENOSINE DIPHOSPHATE AND ITS REVERSAL [J].
BORN, GVR .
NATURE, 1962, 194 (4832) :927-&
[3]  
COTTRELL B A, 1976, Biochimica et Biophysica Acta, V453, P426, DOI 10.1016/0005-2795(76)90138-0
[4]  
COX D, 1992, THROMB HAEMOSTASIS, V68, P731
[5]   ANALYSIS OF PRIMARY STRUCTURE OF COLLAGEN FOR ORIGINS OF MOLECULAR PACKING [J].
HULMES, DJS ;
MILLER, A ;
PARRY, DAD ;
PIEZ, KA ;
WOODHEAD.J .
JOURNAL OF MOLECULAR BIOLOGY, 1973, 79 (01) :137-148
[6]   A NOVEL ARG-GLY-ASP CONTAINING PEPTIDE SPECIFIC FOR PLATELET-AGGREGATION AND ITS EFFECT ON TUMOR-METASTASIS - A POSSIBLE MECHANISM OF RGD PEPTIDE-MEDIATED INHIBITION OF TUMOR-METASTASIS [J].
ISOAI, A ;
UENO, Y ;
GIGAHAMA, Y ;
GOTO, H ;
KUMAGAI, H .
CANCER LETTERS, 1992, 65 (03) :259-264
[7]   ISOLATION AND CHARACTERIZATION OF N-TERMINAL FRAGMENTS OBTAINED BY PLASMIN DIGESTION OF HUMAN FIBRINOGEN [J].
IWANAGA, S ;
WALLEN, P ;
GRONDAHL, NJ ;
HENSCHEN, A ;
BLOMBACK, B .
BIOCHIMICA ET BIOPHYSICA ACTA, 1967, 147 (03) :606-&
[8]   SYNTHETIC PEPTIDE DERIVATIVES THAT BIND TO FIBRINOGEN AND PREVENT POLYMERIZATION OF FIBRIN MONOMERS [J].
LAUDANO, AP ;
DOOLITTLE, RF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (07) :3085-3089
[9]   STUDIES ON SYNTHETIC PEPTIDES THAT BIND TO FIBRINOGEN AND PREVENT FIBRIN POLYMERIZATION - STRUCTURAL REQUIREMENTS, NUMBER OF BINDING-SITES, AND SPECIES-DIFFERENCES [J].
LAUDANO, AP ;
DOOLITTLE, RF .
BIOCHEMISTRY, 1980, 19 (05) :1013-1019
[10]  
LEGER D, 1985, HAEMOSTASIS, V15, P293