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一种新型血栓素合成酶抑制剂在花生四烯酸诱导的猝死中的保护作用。

Protective actions of a new thromboxane synthetase inhibitor in arachidonate induced sudden death.

作者信息

Edmonds L C, Lefer A M

出版信息

Life Sci. 1984 Oct 22;35(17):1763-8. doi: 10.1016/0024-3205(84)90273-x.

Abstract

A new thromboxane synthetase inhibitor, OKY-046, at doses of 0.5 and 1.0 mg/kg prevented mortality induced by sodium arachidonate in 100% of the rabbits studied. Sodium arachidonate at a dose of 1.25 mg/kg uniformly decreased mean arterial blood pressure to values approximately 0 mm Hg, stopped respiration and produced sudden death within 3-5 minutes in all rabbits studied. OKY-046 prevented all these sequelae of the sodium arachidonate. Untreated rabbits challenged with sodium arachidonate develop large increases in circulating thromboxane B2 (TxB2) and 6-keto PGF1 alpha of about 12- to 18-fold. In contrast, OKY-046 prevented the increase in TxB2 concentrations and the pulmonary thrombosis, but did not block the rise in 6-keto PGF1 alpha following arachidonate injection. These results suggest that the protective mechanism of OKY-046 in arachidonate induced sudden death is via selective inhibition of thromboxane synthesis.

摘要

一种新的血栓素合成酶抑制剂OKY - 046,以0.5和1.0毫克/千克的剂量可使100%接受研究的兔子免于花生四烯酸钠诱导的死亡。1.25毫克/千克剂量的花生四烯酸钠可使所有接受研究的兔子的平均动脉血压均匀下降至约0毫米汞柱,停止呼吸并在3 - 5分钟内导致猝死。OKY - 046可预防花生四烯酸钠的所有这些后果。未接受治疗而受到花生四烯酸钠攻击的兔子,循环血栓素B2(TxB2)和6 - 酮前列腺素F1α大幅增加,约为12至18倍。相比之下,OKY - 046可预防TxB2浓度的增加和肺血栓形成,但不能阻止花生四烯酸注射后6 - 酮前列腺素F1α的升高。这些结果表明,OKY - 046对花生四烯酸诱导的猝死的保护机制是通过选择性抑制血栓素合成。

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