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血栓素合成酶抑制对花生四烯酸代谢及血小板行为的影响。

Effects of thromboxane synthetase inhibition on arachidonate metabolism and platelet behaviour.

作者信息

Parry M J

出版信息

Br J Clin Pharmacol. 1983;15 Suppl 1(Suppl 1):23S-29S. doi: 10.1111/j.1365-2125.1983.tb02103.x.

Abstract

1 The effects of the thromboxane synthetase inhibitor dazoxiben (UK 37248) on arachidonic acid and collagen-induced platelet aggregation and arachidonate acid metabolism were studied both in vitro and ex vivo in the presence and absence of sources of prostaglandin I2 synthetase. 2 In platelets activated by exogenous arachidonic acid, the anti-aggregatory activity of dazoxiben was weak compared with indomethacin, despite comparable inhibition of TXB2 production. This was due to the accumulation of pro-aggregatory metabolites, principally endoperoxides. 3 The anti-aggregatory activity of dazoxiben, both in vitro and ex vivo, was higher and more consistent when platelets were stimulated by collagen, threshold levels of which resulted in an endoperoxide accumulation only 2-3% of that achieved with exogenous arachidonic acid. 4 The anti-aggregatory activity of dazoxiben is enhanced if drug equilibration is facilitated by prolonging the preincubation time from 2 to 15 minutes. 5 Incubation of platelets with pig aortic microsomes, which act both as aggregant and a source of PGI2 synthetase, facilitates the conversion to PGI2 of some endoperoxides accumulated after dazoxiben, resulting in augmented anti-aggregatory activity. 6 Leukocytes as well as blood vessels have the capacity to generate PGI2 from platelet derived endoperoxides. This was demonstrated by the increases in 6-keto-PGF1 alpha accompanying decreased TXB2 production in clotted whole blood from volunteers treated with dazoxiben. 7 It was concluded that a closer approach to in vivo conditions allowing a fuller expression of the mechanism of action of dazoxiben could be achieved in vitro by stimulating platelets with a pathophysiological activator such as collagen in the presence of a source of PGI2 synthetase.

摘要
  1. 在有和没有前列腺素I2合成酶来源的情况下,研究了血栓素合成酶抑制剂达唑氧苯(UK 37248)对花生四烯酸和胶原诱导的血小板聚集以及花生四烯酸代谢的体内外作用。2. 在外源性花生四烯酸激活的血小板中,尽管达唑氧苯对TXB2生成的抑制作用相当,但与吲哚美辛相比,其抗聚集活性较弱。这是由于促聚集代谢产物,主要是内过氧化物的积累。3. 当血小板由胶原刺激时,达唑氧苯的体外和体内抗聚集活性更高且更一致,其阈值水平导致的内过氧化物积累仅为外源性花生四烯酸所达到水平的2 - 3%。4. 如果将预孵育时间从2分钟延长至15分钟以促进药物平衡,则达唑氧苯的抗聚集活性会增强。5. 用猪主动脉微粒体孵育血小板,猪主动脉微粒体既是聚集剂又是PGI2合成酶的来源,这有助于将达唑氧苯作用后积累的一些内过氧化物转化为PGI2,从而增强抗聚集活性。6. 白细胞以及血管有能力从血小板衍生的内过氧化物生成PGI2。这在接受达唑氧苯治疗的志愿者的凝血全血中得到了证明,伴随TXB2生成减少,6 - 酮 - PGF1α增加。7. 得出的结论是,通过在PGI2合成酶来源存在的情况下用胶原等病理生理激活剂刺激血小板,在体外可以更接近体内条件,从而更充分地表达达唑氧苯的作用机制。

相似文献

10
Effect of dazoxiben on platelet-vessel wall interaction.达唑氧苯对血小板-血管壁相互作用的影响。
Br J Clin Pharmacol. 1983;15 Suppl 1(Suppl 1):45S-46S. doi: 10.1111/j.1365-2125.1983.tb02106.x.

本文引用的文献

5
Beneficial effects of a new thromboxane synthetase inhibitor in arachidonate-induced sudden death.
Thromb Res. 1981 Aug 1;23(3):265-73. doi: 10.1016/0049-3848(81)90016-5.

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