14,15-EPOXYEICOSATRIENOIC ACID INHIBITS PLATELET-AGGREGATION IN MOUSE CEREBRAL ARTERIOLES

被引:51
作者
HEIZER, ML [1 ]
MCKINNEY, JS [1 ]
ELLIS, EF [1 ]
机构
[1] VIRGINIA COMMONWEALTH UNIV, MED COLL VIRGINIA, DEPT PHARMACOL & TOXICOL, BOX 613, RICHMOND, VA 23298 USA
关键词
ARACHIDONIC ACID; MICROCIRCULATION; PLATELET AGGREGATION; MICE;
D O I
10.1161/01.STR.22.11.1389
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose: Epoxygenase metabolites of arachidonic acid are produced by several tissues and have been shown to inhibit in vitro platelet aggregation. The purpose of the present investigation was to determine whether 14,15- or 8,9-epoxyeicosatrienoic acid, epoxygenase derivatives of arachidonic acid, affect the speed of platelet aggregation in in vivo mouse cerebral arterioles. Methods: We performed a craniectomy in 116 anesthetized male mice and observed the pial arterioles by microscopy. We induced in situ platelet aggregation using a mercury light and intravascularly injected fluorescein dye. Results: Indomethacin (0.5 mg/kg i.p.), a known cyclooxygenase inhibitor, and 14,15-epoxyeicosatrienoic acid (0.3 mg/kg i.v.) increased the time necessary for the light plus dye to induce the first arterial platelet aggregate by 35% and 26%, respectively, whereas 8,9-epoxyeicosatrienoic acid (0.3 mg/kg i.v.) had no effect. Analysis of mouse serum by radioimmunoassay showed that the degree of inhibition of platelet aggregation by indomethacin and epoxyeicosatrienoic acids correlated with the degree of inhibition of thromboxane production. Conclusions: We conclude that 14,15-epoxyeicosatrienoic acid is a potent inhibitor of in vivo platelet aggregation but cannot conclusively confirm that its effect on aggregation occurs via its reduction of platelet thromboxane A2. Because epoxyeicosatrienoic acids are produced by several tissues, including brain and vascular tissue, they may be important in vivo modulators of platelet aggregation and hemostasis.
引用
收藏
页码:1389 / 1393
页数:5
相关论文
共 23 条
  • [11] HEIZER ML, 1991, FASEB J, V5, pA676
  • [12] EFFECTS OF NEWLY REPORTED ARACHIDONIC-ACID METABOLITES ON MICROSOMAL CA++ BINDING, UPTAKE AND RELEASE
    KUTSKY, P
    FALCK, JR
    WEISS, GB
    MANNA, S
    CHACOS, N
    CAPDEVILA, J
    [J]. PROSTAGLANDINS, 1983, 26 (01): : 13 - 21
  • [13] METABOLISM OF ARACHIDONATE THROUGH NADPH-DEPENDENT OXYGENASE OF RENAL CORTEX
    MORRISON, AR
    PASCOE, N
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (12): : 7375 - 7378
  • [14] INVOLVEMENT OF EICOSANOIDS IN RELEASE OF OXYTOCIN AND VASOPRESSIN FROM THE NEURAL LOBE OF THE RAT PITUITARY
    NEGROVILAR, A
    SNYDER, GD
    FALCK, JR
    MANNA, S
    CHACOS, N
    CAPDEVILA, J
    [J]. ENDOCRINOLOGY, 1985, 116 (06) : 2663 - 2668
  • [15] OLIW EH, 1981, J BIOL CHEM, V256, P9924
  • [16] OLIW EH, 1982, J BIOL CHEM, V257, P3771
  • [17] INTESTINAL VASODILATION BY EPOXYEICOSATRIENOIC ACIDS - ARACHIDONIC-ACID METABOLITES PRODUCED BY A CYTOCHROME-P450 MONOOXYGENASE
    PROCTOR, KG
    FALCK, JR
    CAPDEVILA, J
    [J]. CIRCULATION RESEARCH, 1987, 60 (01) : 50 - 59
  • [18] PLATELET-AGGREGATION IN CEREBRAL MICROCIRCULATION - EFFECT OF ASPIRIN AND OTHER AGENTS
    ROSENBLUM, WI
    ELSABBAN, F
    [J]. CIRCULATION RESEARCH, 1977, 40 (03) : 320 - 328
  • [19] SYNTHESIS OF LIPOXYGENASE AND EPOXYGENASE PRODUCTS OF ARACHIDONIC-ACID BY NORMAL AND STENOSED CANINE CORONARY-ARTERIES
    ROSOLOWSKY, M
    FALCK, JR
    WILLERSON, JT
    CAMPBELL, WB
    [J]. CIRCULATION RESEARCH, 1990, 66 (03) : 608 - 621
  • [20] TREATMENT WITH TIN PREVENTS THE DEVELOPMENT OF HYPERTENSION IN SPONTANEOUSLY HYPERTENSIVE RATS
    SACERDOTI, D
    ESCALANTE, B
    ABRAHAM, NG
    MCGIFF, JC
    LEVERE, RD
    SCHWARTZMAN, ML
    [J]. SCIENCE, 1989, 243 (4889) : 388 - 390