Takada Junichi, Ibayashi Setsuro, Ooboshi Hiroaki, Ago Tetsuro, Ishikawa Eiichi, Kamouchi Masahiro, Kitazono Takanari, Iida Mitsuo
Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Hypertens Res. 2006 Aug;29(8):621-6. doi: 10.1291/hypres.29.621.
The effects of angiotensin II type 1 receptor blockers (ARBs) on cerebral blood flow (CBF) autoregulation have not been fully clarified. Thus, we examined the acute effect of valsartan, the most selective ARB, on CBF autoregulation in spontaneously hypertensive rats. Intravenous administration of valsartan (0.3 mg/kg) reduced the mean arterial pressure (MAP) from 184+/-5 (mean+/-SEM) to 174+/-5 mmHg (p<0.001) without affecting CBF as measured by laser-Doppler flowmetry. The lower limit of CBF autoregulation (the MAP at which the CBF was 80% of the baseline value) in the valsartan-treated group (122+/-3 mmHg) was significantly lower than that in the control group (135+/-4 mmHg, p<0.05). Reverse transcribed-polymerase chain reaction and immunohistochemical staining demonstrated that both angiotensin II type 2 receptors and angiotensin II type 1 receptors (AT1Rs) were expressed in endothelial and smooth muscle cells of the rat cerebral arteries. These results suggest that specific inhibition of AT1Rs in the cerebral circulation causes the leftward shift of the lower limit of autoregulation.
血管紧张素II 1型受体阻滞剂(ARB)对脑血流量(CBF)自身调节的影响尚未完全阐明。因此,我们研究了最具选择性的ARB缬沙坦对自发性高血压大鼠CBF自身调节的急性作用。静脉注射缬沙坦(0.3mg/kg)可使平均动脉压(MAP)从184±5(均值±标准误)降至174±5mmHg(p<0.001),而通过激光多普勒血流仪测量发现其不影响CBF。缬沙坦治疗组CBF自身调节的下限(即CBF为基线值80%时的MAP)为122±3mmHg,显著低于对照组(135±4mmHg,p<0.05)。逆转录-聚合酶链反应和免疫组织化学染色表明,血管紧张素II 2型受体和血管紧张素II 1型受体(AT1R)均在大鼠脑动脉的内皮细胞和平滑肌细胞中表达。这些结果表明,脑循环中AT1R的特异性抑制导致自身调节下限向左移位。