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前列环素(PGI2)在猫体内的肺血管舒张活性。

Pulmonary vasodilator activity of prostacyclin (PGI2) in the cat.

作者信息

Hyman A L, Kadowitz P J

出版信息

Circ Res. 1979 Sep;45(3):404-9. doi: 10.1161/01.res.45.3.404.

Abstract

We studied the pulmonary vascular effects of prostacylin, PGI2, in the cat with intact chest under conditions of controlled blood flow. Intralobar injections of PGI2, 0.03--1 microgram, decreased arterial pressure in the perfused lobe in a dose-dependent manner. Inasmuch as lobar blood flow was held constant and left artrial pressure was unchanged, the fall in lobar arterial pressure reflects a decrease in lobar vascular resistance. Prostaglandin E1 (PGE1) and nitroglycerin also decreased lobar arterial pressure; however, PGI2 had greater vasodilator activity than did these substances. Vasodilator responses to PGI2, PGE1, and nitroglycerin in absolute terms were dependent on the baseline level of tone in the pulmonary vascular bed. Prostacyclin reversed the hypertensive and platelet aggregating effects of ADP in the lobar vascular bed. These data indicate that PGI2 has significant vasodilator activity in the feline pulmonary lobar vascular bed.

摘要

我们在血流得到控制的情况下,对完整胸腔猫体内前列腺素(PGI2)的肺血管效应进行了研究。叶内注射0.03 - 1微克的PGI2,可使灌注肺叶的动脉压呈剂量依赖性降低。由于肺叶血流量保持恒定且左心房压力未变,肺叶动脉压的下降反映了肺叶血管阻力的降低。前列腺素E1(PGE1)和硝酸甘油也可降低肺叶动脉压;然而,PGI2的血管舒张活性比这些物质更强。就绝对值而言,对PGI2、PGE1和硝酸甘油的血管舒张反应取决于肺血管床的基础张力水平。前列环素可逆转ADP在肺叶血管床的升压和血小板聚集效应。这些数据表明,PGI2在猫肺叶血管床具有显著的血管舒张活性。

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