Osol G, Laher I, Kelley M
Department of Obstetrics and Gynecology, University of Vermont College of Medicine, Burlington 05405.
Am J Physiol. 1993 Jul;265(1 Pt 2):H415-20. doi: 10.1152/ajpheart.1993.265.1.H415.
The cellular transduction mechanisms underlying the response of blood vessels to mechanical forces such as pressure or stretch are largely unknown. In this report we test the hypothesis that myogenic tone in the cerebral circulation is coupled to activation of phospholipase C (PLC) and G proteins. Rat posterior cerebral arteries (luminal diam 189 +/- 4 microns) were cannulated in an arteriograph and allowed to develop myogenic tone at 75 mmHg (122 +/- 6 microns; P < 0.01). Exposure to U-73122, an inhibitor of PLC, produced concentration-dependent vasodilation, with near-maximal (> 90%) inhibition at concentrations > 3 microM (50% inhibitory concentration = 0.8 +/- 0.04 microM). The action of U-73122 was confirmed by demonstrating that constrictor responses to serotonin (PLC mediated) could be significantly attenuated or abolished at concentrations (0.5-1 microM) that were ineffective in antagonizing potassium depolarization or indolactam-induced constrictions (both PLC independent). Incubation in pertussis toxin (100 ng/ml, 2-2.5 h), an inhibitor of some G protein subtypes, reduced myogenic tone by 74 +/- 12%, with luminal diameters increasing from 129 +/- 7 to 160 +/- 7 microns. Conversely, nonspecific G protein activation using AlF-4 (NaF+AlCl3, 0.5-5 mM) significantly increased myogenic tone by 86 +/- 9%, reducing luminal diameters from 132 +/- 6 to 88 +/- 8 microns (P < 0.01). Together, these findings suggest that 1) PLC is activated in arteries that possess myogenic tone, 2) pharmacological inhibition of PLC results in a virtual loss of pressure-induced constriction, and 3) G proteins may modulate mechanotransduction through pathways superimposed on basal myogenic tone.
血管对诸如压力或拉伸等机械力产生反应的细胞转导机制在很大程度上尚不清楚。在本报告中,我们检验了以下假设:脑循环中的肌源性张力与磷脂酶C(PLC)和G蛋白的激活相关联。将大鼠大脑后动脉(管腔直径189±4微米)插管至血管造影仪中,并使其在75 mmHg压力下产生肌源性张力(122±6微米;P<0.01)。暴露于PLC抑制剂U-73122会产生浓度依赖性血管舒张,在浓度>3 microM时接近最大抑制(>90%)(半数抑制浓度=0.8±0.04 microM)。通过证明在对拮抗钾去极化或吲哚内酰胺诱导的收缩无效的浓度(0.5-1 microM)下,对5-羟色胺(PLC介导)的收缩反应可被显著减弱或消除,证实了U-73122的作用(两者均不依赖PLC)。用百日咳毒素(100 ng/ml,2-2.5小时)孵育,百日咳毒素是一些G蛋白亚型的抑制剂,可使肌源性张力降低74±12%,管腔直径从129±7微米增加到160±7微米。相反,使用AlF-4(NaF+AlCl3,0.5-5 mM)进行非特异性G蛋白激活可使肌源性张力显著增加86±9%,管腔直径从132±6微米减小到88±8微米(P<0.01)。总之,这些发现表明:1)在具有肌源性张力的动脉中PLC被激活;2)对PLC的药理学抑制导致压力诱导的收缩几乎丧失;3)G蛋白可能通过叠加在基础肌源性张力上的途径调节机械转导。