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抗凝剂的作用机制:凝血酶原合成抑制与维生素K1环氧化物向维生素K1再生之间的相关性。

Mechanism of action of anticoagulants: correlation between the inhibition of prothrombin synthesis and the regeneration of vitamin K1 from vitamin K1 epoxide.

作者信息

Ren P, Stark P Y, Johnson R L, Bell R G

出版信息

J Pharmacol Exp Ther. 1977 Jun;201(3):541-6.

PMID:864593
Abstract

It has been proposed that coumarin and indandione anticoagulants inhibit clotting protein synthesis by preventing the regeneration of vitamin K1 from its 2,3-epoxide metabolic. To test this hypothesis, the effects of nine coumarin and indandiones on prothrombin synthesis and the conversion of vitamin K1 epoxide to vitamin K1 were measured. There was a good correlation between the inhibition of prothrombin synthesis and the epoxide-K1 conversion both in vivo and in vitro. Diphenadione (2-diphenyl acetyl-1,3-indandione) caused a delayed inhibition of prothrombin synthesis which correlated with a delayed inhibition of the epoxide-K1 conversion in vivo. These results provide strong evidence for the proposed mechanism of action of coumarin and indandione anticoagulants.

摘要

有人提出香豆素类和茚二酮类抗凝剂通过阻止维生素K1从其2,3-环氧化物代谢产物再生来抑制凝血蛋白的合成。为了验证这一假设,测定了9种香豆素类和茚二酮类药物对凝血酶原合成以及维生素K1环氧化物向维生素K1转化的影响。在体内和体外,凝血酶原合成的抑制与环氧化物-K1转化之间均存在良好的相关性。双苯茚酮(2-二苯基乙酰基-1,3-茚二酮)导致凝血酶原合成延迟抑制,这与体内环氧化物-K1转化的延迟抑制相关。这些结果为香豆素类和茚二酮类抗凝剂的作用机制提供了有力证据。

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