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新型血栓素A2抑制剂BM - 573给药前后U - 46619对肺血流动力学的影响。

Effects of U-46619 on pulmonary hemodynamics before and after administration of BM-573, a novel thromboxane A2 inhibitor.

作者信息

Lambermont B, Kolh P, Dogné J-M, Ghuysen A, Tchana-Sato V, Morimont P, Benoit P, Gérard P, Masereel B, Limet R, D'Orio V

机构信息

Hemodynamics Research Laboratory (HemoLiege), University of Liège, Belgium.

出版信息

Arch Physiol Biochem. 2003 Jul;111(3):217-23. doi: 10.1076/apab.111.3.217.23459.

DOI:10.1076/apab.111.3.217.23459
PMID:14972743
Abstract

We studied the effects on pulmonary hemodynamics of U-46619, a thromboxane A2 (TXA2) agonist, before and after administration of a novel TXA2 receptor antagonist and synthase inhibitor (BM-573). Six anesthetized pigs (Ago group) received 6 consecutive injections of U-46619 at 30-min interval and were compared with six anesthetized pigs (Anta group) which received an increasing dosage regimen of BM-573 10 min before each U-46619 injection. Consecutive changes in pulmonary hemodynamics, including characteristic resistance, vascular compliance, and peripheral vascular resistance, were continuously assessed during the experimental protocol using a four-element Windkessel model. At 2 mg/kg, BM-573 completely blocked pulmonary hypertensive effects of U-46619 but pulmonary vascular compliance still decreased. This residual effect can probably be explained by a persistent increase in the tonus of the pulmonary vascular wall smooth muscles sufficient to decrease vascular compliance but not vessel lumen diameter. Such molecule could be a promising therapeutic approach in TXA2 mediated pulmonary hypertension as it is the case in pulmonary embolism, hyperacute lung rejection and endotoxinic shock.

摘要

我们研究了血栓素A2(TXA2)激动剂U-46619在给予新型TXA2受体拮抗剂和合成酶抑制剂(BM-573)前后对肺血流动力学的影响。六只麻醉猪(Ago组)每隔30分钟连续注射6次U-46619,并与六只麻醉猪(Anta组)进行比较,后者在每次注射U-46619前10分钟接受递增剂量方案的BM-573。在实验过程中,使用四元件Windkessel模型持续评估肺血流动力学的连续变化,包括特征性阻力、血管顺应性和外周血管阻力。在2mg/kg时,BM-573完全阻断了U-46619的肺动脉高压作用,但肺血管顺应性仍降低。这种残余效应可能可以用肺血管壁平滑肌张力持续增加来解释,这种增加足以降低血管顺应性,但不会减小血管腔直径。这种分子可能是TXA2介导的肺动脉高压的一种有前景的治疗方法,就像在肺栓塞、超急性肺排斥和内毒素休克中一样。

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