Segal Steven S
The John B. Pierce Laboratory & Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06519, USA.
Microcirculation. 2005 Jan-Feb;12(1):33-45. doi: 10.1080/10739680590895028.
The regulation of blood flow has rich history of investigation and is exemplified in exercising skeletal muscle by a concerted interaction between striated muscle fibers and their microvascular supply. This review considers blood flow control in light of the regulation of capillary perfusion by and among terminal arterioles, the distribution of blood flow in arteriolar networks according to metabolic and hemodynamic feedback from active muscle fibers, and the balance between peak muscle blood flow and arterial blood pressure governed by sympathetic nerve activity. As metabolic demand increases,the locus of regulating oxygen delivery to muscle fibers "ascends" from terminal arterioles, through intermediate distributing arterioles, and into the proximal arterioles and feed arteries, which govern total flow into a muscle. At multiple levels, venules are positioned to provide feedback to nearby arterioles regarding the metabolic state of the tissue through the convection, production and diffusion of vasodilator stimuli. Electrical signals initiated on microvascular smooth muscle and endothelial cells can travel rapidly for millimeters through cell-to-cell conduction via gap junction channels, rapidly coordinating vasodilator responses that govern the distribution and magnitude of blood flow to active muscle fibers. Sympathetic constriction of proximal arterioles and feed arteries can restrict functional hyperemia while dilation prevails in distal arterioles to promote oxygen extraction. With vasomotor tone reflecting myogenic contraction of smooth muscle cells modulated by shear stress on the endothelium, the initiation of functional vasodilation and its modulation by sympathetic innervation dictate how and where blood flow is distributed in response to metabolic demand. A remarkable ensemble of signaling pathways underlies the integration of smooth muscle and endothelial cell function in microvascular networks. These pathways are being defined with refreshing new insight as novel approaches are applied to understanding the cellular and molecular mechanisms of blood flow control.
血流调节有着丰富的研究历史,在运动的骨骼肌中,横纹肌纤维与其微血管供应之间的协同相互作用就是一个例证。本综述从终末小动脉之间以及终末小动脉对毛细血管灌注的调节、根据活跃肌纤维的代谢和血流动力学反馈在小动脉网络中的血流分布、以及由交感神经活动控制的肌肉峰值血流与动脉血压之间的平衡等方面来探讨血流控制。随着代谢需求增加,调节向肌纤维输送氧气的部位从终末小动脉“上升”至中间分布小动脉,再到近端小动脉和供血动脉,后者控制着进入肌肉的总血流量。在多个层面上,微静脉能够通过血管舒张刺激物的对流、产生和扩散,就组织的代谢状态向附近的小动脉提供反馈。在微血管平滑肌和内皮细胞上启动的电信号可通过缝隙连接通道在细胞间迅速传导数毫米,快速协调血管舒张反应,从而控制流向活跃肌纤维的血流分布和大小。近端小动脉和供血动脉的交感神经收缩可限制功能性充血,而远端小动脉则以扩张为主以促进氧气摄取。血管舒缩张力反映了内皮上剪切应力调节的平滑肌细胞的肌源性收缩,功能性血管舒张的启动及其受交感神经支配的调节决定了血流如何以及在何处根据代谢需求进行分布。微血管网络中平滑肌和内皮细胞功能的整合有着一系列显著的信号通路作为基础。随着新方法被应用于理解血流控制的细胞和分子机制,这些通路正以全新的视角被阐释。