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清醒犬前列腺素合成抑制后的肺升压反应

Pulmonary pressor response after prostaglandin synthesis inhibition in conscious dogs.

作者信息

Walker B R, Voelkel N F, Reeves J T

出版信息

J Appl Physiol Respir Environ Exerc Physiol. 1982 Mar;52(3):705-9. doi: 10.1152/jappl.1982.52.3.705.

Abstract

Recent studies have shown that vasodilator prostaglandins are continually produced by the isolated rat lung. We postulated that these vasodilators may contribute to maintenance of normal low pulmonary arterial pressure. Pulmonary pressure and cardiac output were measured in conscious dogs prior to and 30 to 60 min following administration of meclofenamate (2 mg/kg iv, followed by infusion at 2 mg . kg-1 . h-1) or the structurally dissimilar inhibitor RO-20-5720 (1 mg/kg iv, followed by infusion at 1 mg . kg-1 . h-1). The animals were also made hypoxic with inhalation of 10% O2 before and after inhibition. Time-control experiments were conducted in which only the saline vehicle was administered. Meclofenamate or RO-20-5720 caused an increase in mean pulmonary arterial pressure and total pulmonary resistance. Cardiac output and systemic pressure were unaffected. The mild hypoxic pulmonary pressor response observed was not affected by meclofenamate. Animals breathing 30% O2 to offset Denver's altitude also demonstrated increased pulmonary pressure and resistance when given meclofenamate. It is concluded that endogenous vasodilator prostaglandins may contribute to normal, low vascular tone in the pulmonary circulation.

摘要

最近的研究表明,离体大鼠肺持续产生血管舒张性前列腺素。我们推测这些血管舒张剂可能有助于维持正常的低肺动脉压。在清醒犬静脉注射甲氯芬那酸(2mg/kg,随后以2mg·kg⁻¹·h⁻¹输注)或结构不同的抑制剂RO-20-5720(1mg/kg静脉注射,随后以1mg·kg⁻¹·h⁻¹输注)之前及之后30至60分钟,测量其肺压和心输出量。在抑制前后,动物还通过吸入10%氧气造成低氧状态。进行了仅给予生理盐水载体的时间对照实验。甲氯芬那酸或RO-20-5720导致平均肺动脉压和总肺阻力增加。心输出量和体循环压力未受影响。观察到的轻度低氧性肺血管收缩反应不受甲氯芬那酸影响。吸入30%氧气以抵消丹佛海拔高度影响的动物在给予甲氯芬那酸后也表现出肺压和阻力增加。结论是内源性血管舒张性前列腺素可能有助于肺循环中正常的低血管张力。

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