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五种血管紧张素I转换酶抑制剂对自发性高血压大鼠的全身和局部血流动力学影响

Systemic and regional hemodynamic profile of five angiotensin I converting enzyme inhibitors in the spontaneously hypertensive rat.

作者信息

Richer C, Doussau M P, Giudicelli J F

出版信息

Am J Cardiol. 1987 Apr 24;59(10):12D-17D. doi: 10.1016/0002-9149(87)90046-4.

Abstract

The effects of 5 angiotensin I converting enzyme (ACE) inhibitors--captopril, enalapril, perindopril, trandolapril and ramipril--on general and regional hemodynamics were investigated (using radioactive microspheres) and compared in anesthetized adult spontaneously hypertensive rats. The 5 treatments were administered daily by gavage for 8 days in doses inducing identical decreases in arterial blood pressure. This effect was entirely due to a decrease in total peripheral resistance inasmuch as cardiac index was not affected by the 5 ACE inhibitors. In addition, despite their different chemical structures, all exhibited the same regional vasodilator pattern, which thus appears to be related only to ACE inhibition. The vascular beds resistances were decreased in the following order: renal greater than splenic = liver greater than skin greater than total peripheral greater than muscle = brain. Simultaneously, and despite the decrease in perfusion pressure, most regional blood flows and especially renal blood flow were increased. Finally, renal vasodilator effects of ACE inhibitors were observed even after doses that lacked any effect on total peripheral resistance.

摘要

研究了5种血管紧张素I转换酶(ACE)抑制剂——卡托普利、依那普利、培哚普利、群多普利和雷米普利——对麻醉的成年自发性高血压大鼠整体和局部血流动力学的影响(使用放射性微球)并进行了比较。这5种药物每日经口灌胃给药8天,剂量能使动脉血压出现相同程度的下降。这种作用完全归因于总外周阻力的降低,因为心脏指数不受这5种ACE抑制剂的影响。此外,尽管它们化学结构不同,但都呈现相同的局部血管舒张模式,因此这种模式似乎仅与ACE抑制有关。血管床阻力降低的顺序如下:肾>脾 = 肝>皮肤>总外周>肌肉 = 脑。同时,尽管灌注压降低,但大多数局部血流量尤其是肾血流量增加。最后,即使在对总外周阻力无任何影响的剂量下,也观察到了ACE抑制剂的肾血管舒张作用。

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