INFLUENCE OF DIETARY FISH ON EICOSANOID METABOLISM IN MAN

被引:12
作者
HONSTRA, G
VANHOUWELINGEN, AC
KIVITS, GAA
FISCHER, S
UEDELHOVEN, W
机构
[1] UNILEVER RES, DEPT BIOSCI NUTR & SAFETY, VLAARDINGEN, NETHERLANDS
[2] UNIV MUNICH, KLINIKUM GROSSHADERN, W-8000 MUNICH 2, GERMANY
[3] UNIV MUNICH, INST PROPHYLAXE KREISLAUFKRANKHEITEN, W-8000 MUNICH 2, GERMANY
关键词
D O I
10.1016/0090-6980(90)90018-Q
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
Two groups of 40 volunteers were given a dietary supplement consisting of 135 g of mackerel or meat (control) paste per day for 6 weeks. Compliance was about 80% in both groups and the daily intake of 20:5(n-3) and 22:6(n-3) from the mackerel supplement was about 1.3 and 2.3 g, respectively. In collagen-activated platelet rich plasma, the potency of blood platelet to produced HHT from arachidonic acid (AA) clearly reduced in the mackerel group, whereas the formation of HHTE from timnodonic acid (TA) increased slightly. Changes in the formation of HHT and HHTE, measured by HPLC, correlated significantly with those of TxB2 and TxB3, respectively, measured by GC/MS. Changes in the formation of the lipoxygenase products HETE (ex AA) and HEPE (ex TA) were qualitatively similar to that seen for the cyco-oxygenase products, but quantitatively the responses were smaller. Formation of ir TxB2 in clotting blood significantly reduced in the mackerel group. In collagen-activated, citrated whole blood, TxB2 formation tended to be reduced in the mackerel-supplemented volunteers. Mackerel consumption was associated with the formation of considerable amounts of PGl3, as judged from the appearance of 2,3-dinor-Δ 17-6-keto-PGF1α in urine. The amount of the major metabolite of PGl2, 2,3-dinor-6-keto-PGF1α was not reduced, or even increased. The daily amount of tetranor prostaglandin metabolites in the urine did not change significantly, which indicates that mackerel supplementation did not alter the formation of prostaglandins E and F. © 1990.
引用
收藏
页码:311 / 329
页数:19
相关论文
共 50 条
[11]  
Dixon W.J., 1951, ANN MATH STAT, V22, P68, DOI [DOI 10.1214/AOMS/1177729693, 10.1214/aoms/1177729693]
[12]   THE ROLE OF ARACHIDONATE LIPOXYGENASE AND FATTY-ACIDS DURING IRREVERSIBLE BLOOD-PLATELET AGGREGATION INVITRO [J].
DUTILH, CE ;
HADDEMAN, E ;
DON, JA ;
TENHOOR, F .
PROSTAGLANDINS AND MEDICINE, 1981, 6 (02) :111-126
[13]  
EMEIS JJ, 1989, BLOOD, V74, P233
[14]   THROMBOXANE-A3 (TXA3) IS FORMED IN HUMAN-PLATELETS AFTER DIETARY EICOSAPENTAENOIC ACID (C2O-5-OMEGA-3) [J].
FISCHER, S ;
WEBER, PC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1983, 116 (03) :1091-1099
[15]   PROSTAGLANDIN-I3 IS FORMED INVIVO IN MAN AFTER DIETARY EICOSAPENTAENOIC ACID [J].
FISCHER, S ;
WEBER, PC .
NATURE, 1984, 307 (5947) :165-168
[16]   THE PROSTACYCLIN THROMBOXANE BALANCE IS FAVORABLY SHIFTED IN GREENLAND ESKIMOS [J].
FISCHER, S ;
WEBER, PC ;
DYERBERG, J .
PROSTAGLANDINS, 1986, 32 (02) :235-241
[17]   INCREASED PROSTACYCLIN BIOSYNTHESIS IN PATIENTS WITH SEVERE ATHEROSCLEROSIS AND PLATELET ACTIVATION [J].
FITZGERALD, GA ;
SMITH, B ;
PEDERSEN, AK ;
BRASH, AR .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (17) :1065-1068
[18]   ESTIMATED RATE OF PROSTACYCLIN SECRETION INTO THE CIRCULATION OF NORMAL MAN [J].
FITZGERALD, GA ;
BRASH, AR ;
FALARDEAU, P ;
OATES, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 68 (05) :1272-1276
[19]   LIPOXYGENASE INHIBITORS ALTER AGGREGATION AND ADHESIVENESS OF HUMAN-BLOOD PLATELETS FROM ASPIRIN-TREATED PATIENTS [J].
GIMENO, MF ;
SHATTNER, MA ;
BORDA, E ;
GIMENO, AL ;
LAZZARI, MA .
PROSTAGLANDINS LEUKOTRIENES AND MEDICINE, 1983, 11 (01) :109-119
[20]   DIETARY LINOLEIC-ACID, GASTRIC-ACID, AND PROSTAGLANDIN SECRETION [J].
GRANT, HW ;
PALMER, KR ;
KELLY, RW ;
WILSON, NH ;
MISIEWICZ, JJ .
GASTROENTEROLOGY, 1988, 94 (04) :955-959