Department of Pharmacology, College of Medicine, University of Vermont, Burlington, Vermont 05405, USA.
J Cereb Blood Flow Metab. 2013 Feb;33(2):293-9. doi: 10.1038/jcbfm.2012.169. Epub 2012 Nov 21.
Myogenic tone is a fundamental aspect of vascular behavior in resistance arteries. This contractile response to changes in intravascular pressure is critically involved in blood flow autoregulation in tissues such as the brain, kidneys, and heart. Myogenic tone also helps regulate precapillary pressure and provides a level of background tone upon which vasodilator stimuli act to increase tissue perfusion when appropriate. Despite the importance of these processes in the brain, little is known about the mechanisms involved in control of myogenic tone in the cerebral microcirculation. Here, we report that pharmacological inhibition of P2Y4 and P2Y6 pyrimidine receptors nearly abolished myogenic tone in cerebral parenchymal arterioles (PAs). Molecular suppression of either P2Y4 or P2Y6 receptors using antisense oligodeoxynucleotides reduced myogenic tone by 44%±8% and 45%±7%, respectively. These results indicate that both receptor isoforms are activated by increased intravascular pressure, which enhances the activity of voltage-dependent calcium channels and increases myogenic tone in PAs. Enhancement or inhibition of ectonucleotidase activity had no effect on parenchymal arteriolar myogenic tone, indicating that this response is not mediated by local release of nucleotides, but rather may involve direct mechanical activation of P2Y receptors in the smooth muscle cells.
肌源性张力是阻力血管行为的一个基本方面。这种对血管内压力变化的收缩反应对于大脑、肾脏和心脏等组织中的血流自动调节至关重要。肌源性张力还有助于调节小动脉前压,并在适当的时候为血管扩张刺激增加组织灌注提供背景张力。尽管这些过程在大脑中非常重要,但对于控制脑微循环中的肌源性张力的机制知之甚少。在这里,我们报告称,嘌呤嘧啶受体 P2Y4 和 P2Y6 的药理学抑制几乎消除了脑实质小动脉(PA)中的肌源性张力。使用反义寡脱氧核苷酸对 P2Y4 或 P2Y6 受体进行分子抑制,分别使肌源性张力降低了 44%±8%和 45%±7%。这些结果表明,这两种受体亚型都被升高的血管内压激活,这增强了电压依赖性钙通道的活性并增加了 PA 中的肌源性张力。外核苷酸酶活性的增强或抑制对实质小动脉的肌源性张力没有影响,这表明该反应不是由局部核苷酸释放介导的,而是可能涉及平滑肌细胞中 P2Y 受体的直接机械激活。