Joyner W L, Mohama R E, Myers T O, Gilmore J P
Department of Physiology and Biophysics, University of Nebraska College of Medicine, Omaha.
Microvasc Res. 1988 Jan;35(1):122-31. doi: 10.1016/0026-2862(88)90055-6.
The present study was undertaken to investigate the effect of adenosine on the microvasculature of the hamster kidney and the possibility of angiotensin II mediation. Renal tissue from neonatal hamsters was grafted into the cheek pouch of 33 adult hamsters. Seven to twelve days later the renal microcirculation was studied. Adenosine was tested on the pre- and postglomerular arterioles as well as on cheek pouch arterioles before and after applying an AII antagonist, saralasin. Adenosine dilated the cheek pouch arterioles and constricted the preglomerular arterioles in a dose-dependent manner. Adenosine had no effect on postglomerular arterioles. The renal vasoconstriction persisted as long as adenosine was present. Theophylline reduced the adenosine-mediated vasoconstriction of the afferent arteriole in a dose-dependent manner. These changes were not altered in the presence of saralasin at various doses, one of which was 20-fold greater than that required to abolish the vasoconstrictor response of a test dose of angiotensin II. This study indicates that the adenosine-mediated vasoconstriction of the preglomerular microvessels is not mediated via the renin-angiotensin system but may be a direct effect of adenosine.
本研究旨在探讨腺苷对仓鼠肾脏微血管系统的影响以及血管紧张素II介导的可能性。将新生仓鼠的肾组织移植到33只成年仓鼠的颊囊中。7至12天后,研究肾脏微循环。在应用血管紧张素II拮抗剂沙拉新之前和之后,对肾小球前和肾小球后小动脉以及颊囊小动脉进行腺苷测试。腺苷以剂量依赖的方式扩张颊囊小动脉并收缩肾小球前小动脉。腺苷对肾小球后小动脉无影响。只要存在腺苷,肾血管收缩就会持续。茶碱以剂量依赖的方式降低腺苷介导的入球小动脉血管收缩。在不同剂量的沙拉新存在下,这些变化没有改变,其中一种剂量比消除测试剂量血管紧张素II的血管收缩反应所需剂量大20倍。这项研究表明,腺苷介导的肾小球前微血管血管收缩不是通过肾素-血管紧张素系统介导的,可能是腺苷的直接作用。