ARACHIDONIC-ACID METABOLISM IN PLATELETS STORED FOR 5 DAYS

被引:17
作者
CESAR, JM
NAVARRO, JL
机构
关键词
D O I
10.1111/j.1365-2141.1990.tb02586.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
(C‐14)‐Arachidonic acid [(C‐14)‐AA] metabolism was studied in platelet concentrates (PCs) stored for 5 d. There was a gradual decrease in uptake of radioactivity from day 0 to 3 (P < 0.01). On day 0, distribution of radioactivity in platelet phospholipids (PLs), and formation of phosphatidic acid, HETE and cyclooxygenase products, when platelets were exposed to thrombin (5 U/ml), were similar to that reported for fresh platelets. On day 3 there was a change in the distribution of (C‐14)‐AA in platelet PLs which consisted of an increase in the percentage of radioactivity bound to phosphatidylserine, from 5.3±0.9% on day 0 to 8.8±1.5% on day 3 (P<0.001), and a decrease in (C‐14)‐AA in phosphatidylinositol (PI), from 12.4±1.5% on day 0, to 7.9±0.9% on day 3 (P<0.001). Phosphatidic acid generated by thrombin‐stimulated platelets on day 0, comprised 2.6±0.5% of total radioactivity, but dropped to 1.4±0.3% on day 3 (P<0.001), and 0.9±0.2% on day 5 (P<0.01). These values showed a good correlation with the percentage of (C‐14)‐AA released from PI on the same days (r=0‐9). On day 0, 13.4 ± 4.4% of platelet radioactivity was released from phosphatidylcholine by thrombin, but this amount was reduced to 6.8±3.4% on day 5 (P<0.05). Generation of radioactive 12‐hydroxy‐5,8,10,14‐eicosatetraynoic acid (HETE) also dropped from 7.2±2.9 on day 0. to 2.1 ± 1 on day 5 (P< 0.01). We could not detect changes in cyclooxygenase metabolites. In conclusion, we suggest that various enzymatic pathways implicated in AA metabolism by platelets are impaired by storage. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
收藏
页码:295 / 299
页数:5
相关论文
共 33 条
[1]   DIGLYCERIDE LIPASE - PATHWAY FOR ARACHIDONATE RELEASE FROM HUMAN-PLATELETS [J].
BELL, RL ;
KENNERLY, DA ;
STANFORD, N ;
MAJERUS, PW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (07) :3238-3241
[2]   INOSITOL TRISPHOSPHATE, A NOVEL 2ND MESSENGER IN CELLULAR SIGNAL TRANSDUCTION [J].
BERRIDGE, MJ ;
IRVINE, RF .
NATURE, 1984, 312 (5992) :315-321
[3]   SELECTIVE RELEASE OF ARCHIDONIC ACID FROM PHOSPHOLIPIDS OF HUMAN PLATELETS IN RESPONSE TO THROMBIN [J].
BILLS, TK ;
SMITH, JB ;
SILVER, MJ .
JOURNAL OF CLINICAL INVESTIGATION, 1977, 60 (01) :1-6
[4]   METABOLISM OF (C-14) ARACHIDONIC-ACID BY HUMAN PLATELETS [J].
BILLS, TK ;
SMITH, JB ;
SILVER, MJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 424 (02) :303-314
[5]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[6]  
BOLIN RB, 1981, J LAB CLIN MED, V98, P500
[7]   QUANTITATIVE 2-DIMENSIONAL THIN-LAYER CHROMATOGRAPHY OF BLOOD PHOSPHOLIPIDS [J].
BROEKHUYSE, RM .
CLINICA CHIMICA ACTA, 1969, 23 (03) :457-+
[8]  
CALL FL, 1973, J LIPID RES, V14, P466
[9]  
DIMINNO G, 1982, BLOOD, V59, P563
[10]   PLATELET MEMBRANE GLYCOPROTEINS - ALTERATION DURING STORAGE OF HUMAN PLATELET CONCENTRATES [J].
GEORGE, JN .
THROMBOSIS RESEARCH, 1976, 8 (05) :719-724