Näveri L, Strömberg C, Saavedra J M
Section on Pharmacology, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892.
Regul Pept. 1994 Jun 16;52(1):21-9. doi: 10.1016/0167-0115(94)90017-5.
The effects of the angiotensin II (ANG II) AT2 ligand PD 123319 and the AT1 antagonist losartan on cerebral blood flow (CBF) were studied during hemorrhagic hypotension in anesthetized rats using laser-Doppler flowmetry. In the control group CBF remained stable when mean arterial blood pressure (MABP) was lowered from 84 mmHg (baseline) to 45 mmHg, whereafter there was a pressure dependent decrease in CBF indicating inadequacy of autoregulation. Cerebrovascular resistance (CVR) was reduced until MABP 40 mmHg, where a maximum dilation was reached. PD 123319 dose-dependently (3-30 mg/kg i.v.) increased CVR through all blood pressures. Losartan 3 mg/kg i.v. had an effect similar to PD 123319. Selective stimulation of AT2 receptors with intravenous ANG II infusion, in the presence of AT1 receptor blockade by losartan, also increased CVR. As a result, reduced CBF was seen in the treatment groups. The effects of ANG II and PD 123319 30 mg/kg were antagonized by the nonselective ANG II antagonist Sar1,Ile8-ANG II (4 micrograms/kg/min i.v.). None of the treatments affected baseline CBF. The results confirm that ANG II contributes to cerebrovascular resistance and participates in the regulation of CBF apparently through AT2 receptors.
在麻醉大鼠失血性低血压期间,使用激光多普勒血流仪研究了血管紧张素II(ANG II)的AT2配体PD 123319和AT1拮抗剂氯沙坦对脑血流量(CBF)的影响。在对照组中,当平均动脉血压(MABP)从84 mmHg(基线)降至45 mmHg时,CBF保持稳定,此后CBF随压力依赖性下降,表明自动调节功能不足。脑血管阻力(CVR)在MABP降至40 mmHg之前降低,此时达到最大扩张。PD 123319(静脉注射3 - 30 mg/kg)在所有血压水平上均剂量依赖性地增加CVR。静脉注射3 mg/kg氯沙坦具有与PD 123319相似的作用。在氯沙坦阻断AT1受体的情况下,静脉输注ANG II选择性刺激AT2受体也会增加CVR。结果,在治疗组中观察到CBF降低。非选择性ANG II拮抗剂Sar1,Ile8 - ANG II(静脉注射4微克/千克/分钟)可拮抗ANG II和30 mg/kg PD 123319的作用。所有治疗均不影响基线CBF。结果证实,ANG II对脑血管阻力有影响,并且显然通过AT2受体参与CBF的调节。