Oxford Medical School, University of Oxford, Oxford, UK.
Acute Stroke Programme, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Brain. 2022 Jul 29;145(7):2276-2292. doi: 10.1093/brain/awac174.
To match the metabolic demands of the brain, mechanisms have evolved to couple neuronal activity to vasodilation, thus increasing local cerebral blood flow and delivery of oxygen and glucose to active neurons. Rather than relying on metabolic feedback signals such as the consumption of oxygen or glucose, the main signalling pathways rely on the release of vasoactive molecules by neurons and astrocytes, which act on contractile cells. Vascular smooth muscle cells and pericytes are the contractile cells associated with arterioles and capillaries, respectively, which relax and induce vasodilation. Much progress has been made in understanding the complex signalling pathways of neurovascular coupling, but issues such as the contributions of capillary pericytes and astrocyte calcium signal remain contentious. Study of neurovascular coupling mechanisms is especially important as cerebral blood flow dysregulation is a prominent feature of Alzheimer's disease. In this article we will discuss developments and controversies in the understanding of neurovascular coupling and finish by discussing current knowledge concerning neurovascular uncoupling in Alzheimer's disease.
为了满足大脑的代谢需求,已经进化出了一些机制,使神经元活动与血管舒张相耦合,从而增加局部脑血流并向活跃的神经元输送氧气和葡萄糖。主要的信号通路不是依赖于代谢反馈信号(如氧气或葡萄糖的消耗),而是依赖于神经元和星形胶质细胞释放的血管活性分子,这些分子作用于收缩细胞。血管平滑肌细胞和周细胞分别与小动脉和毛细血管相关联,它们的舒张会引起血管扩张。在理解神经血管耦联的复杂信号通路方面已经取得了很大进展,但毛细血管周细胞和星形胶质细胞钙信号的贡献等问题仍然存在争议。研究神经血管耦联机制尤为重要,因为大脑血流失调是阿尔茨海默病的一个突出特征。在本文中,我们将讨论神经血管耦联理解方面的进展和争议,并最后讨论关于阿尔茨海默病中神经血管解耦的当前知识。