Whalley E T, Wahl M
Department of Physiology, University of Munich, F.R.G.
Brain Res. 1988 Jan 12;438(1-2):1-7. doi: 10.1016/0006-8993(88)91318-2.
The purpose of the present study was to test the vasomotor effect of angiotensin I (A I) and angiotensin II (A II) in feline cerebral arteries and to examine the presence of angiotensin converting enzyme (ACE) activity in the vessel wall and cerebrospinal fluid (CSF). A II (10(-8) -10(-5) M) induced concentration-dependent contractions of feline pial arteries (resting diameter, 98-286 microns) in situ with a maximum of 34% at 10(-4) M A II. A I produced dose-related contractions being approximately 20 times less potent than A II. The action of A I was significantly attenuated by the ACE inhibitor captopril (10(-5) M). These findings demonstrate the presence of ACE activity in the vessel wall and/or its surroundings. ACE activity was also found in feline CSF sampled from the cisterna cerebellomedullaris. Bradykinin (BK) was broken down and A I converted to A II by CSF, both effects being inhibited by captopril. This was demonstrated using bioassay and high-performance liquid chromatography. Considering the present and previous studies we conclude that the presence of ACE in the vessel wall and CSF is necessary for the conversion of A I to A II. Although ACE in CSF is able to degrade BK it appears not to be important for the metabolism of BK acting from the perivascular side of pial arteries in situ.
本研究的目的是测试血管紧张素I(AI)和血管紧张素II(AII)对猫脑动脉的血管舒缩作用,并检测血管壁和脑脊液(CSF)中血管紧张素转换酶(ACE)的活性。在体状态下,AII(10⁻⁸ - 10⁻⁵M)可引起猫软脑膜动脉(静息直径为98 - 286微米)浓度依赖性收缩,在10⁻⁴M AII时收缩幅度最大可达34%。AI产生剂量相关的收缩作用,其效力约为AII的20分之一。ACE抑制剂卡托普利(10⁻⁵M)可显著减弱AI的作用。这些发现证明血管壁及其周围存在ACE活性。在从小脑延髓池采集的猫CSF中也发现了ACE活性。缓激肽(BK)可被CSF降解,且AI可被CSF转化为AII,这两种作用均受卡托普利抑制。这通过生物测定法和高效液相色谱法得以证实。综合当前及以往研究,我们得出结论:血管壁和CSF中ACE的存在对于AI转化为AII是必需的。虽然CSF中的ACE能够降解BK,但对于原位软脑膜动脉血管周围侧起作用的BK代谢而言,其似乎并不重要。