Bearden Shawn E
Department of Biological Sciences, Idaho State University, Pocatello, Idaho 83209, USA.
Microcirculation. 2006 Jun;13(4):279-88. doi: 10.1080/10739680600618892.
Humans are active creatures, yet physical activity and activity tolerance decline over the life span. One prevailing theme in the literature to account for a portion of the reduced activity tolerance with aging is the observation that the capacity to augment blood flow to skeletal muscle may be impaired with advancing age. This dysfunction may be due to adaptations in the structure or function of their microvascular networks, which collectively determine blood flow resistance. The intent of this review is to present the current knowledge of structure and function of microvascular networks from skeletal muscle with special regard to how these may adapt to, or persist through, the aging process. Skeletal muscles are supplied by an intricate branching network of arterioles and venules. The consistency of findings among available studies suggests that the overall arteriolar and venular network branching topology establishes early in development and varies little, if at all, over the life span. Microvascular networks are not a series of functionally isolated segmental branches. Rather, these networks transmit and communicate vasomotor signals along their lengths and among their branches. Current evidence suggests that aging is associated with a decrement in the capacity of upstream vessels to respond to downstream vasodilation and signals transmitted cell-to-cell along the vascular wall.
人类是活跃的生物,但身体活动能力和活动耐量会随着寿命的增长而下降。文献中一个普遍的观点是,随着年龄的增长,骨骼肌血流量增加的能力可能受损,这在一定程度上解释了活动耐量下降的原因。这种功能障碍可能是由于其微血管网络的结构或功能发生了适应性变化,这些变化共同决定了血流阻力。本综述的目的是介绍目前关于骨骼肌微血管网络结构和功能的知识,特别关注这些网络如何适应衰老过程或在衰老过程中持续存在。骨骼肌由复杂的小动脉和小静脉分支网络供血。现有研究结果的一致性表明,小动脉和小静脉网络的整体分支拓扑结构在发育早期就已形成,并且在整个生命周期中变化很小,如果有变化的话。微血管网络不是一系列功能上孤立的节段性分支。相反,这些网络在其长度上以及分支之间传递和交流血管舒缩信号。目前的证据表明,衰老与上游血管对下游血管舒张以及沿血管壁细胞间传递信号的反应能力下降有关。