Rembold Christopher M
Box 800146, Cardiovascular Division, Univ. of Virginia Health System, Charlottesville, VA 22908-0146, USA.
Am J Physiol Cell Physiol. 2007 Sep;293(3):C1003-9. doi: 10.1152/ajpcell.00091.2007. Epub 2007 May 23.
Cyclic nucleotides can relax arterial smooth muscle without reductions in crossbridge phosphorylation, a process termed force suppression. There are two potential mechanisms for force suppression: 1) phosphorylated crossbridges binding to thin filaments could be inhibited or 2) the attachment of thin filaments to anchoring structures could be disrupted. These mechanisms were evaluated by comparing histamine-stimulated swine arterial smooth muscle with and without forskolin-induced force suppression and with and without latrunculin-A-induced actin filament disruption. At matched force, force suppression was associated with higher crossbridge phosphorylation and shortening velocity at low loads when compared with tissues without force suppression. Shortening velocity at high loads, noise temperature, hysteresivity, and stiffness did not differ with and without force suppression. These data suggest that crossbridge phosphorylation regulates the crossbridge cycle during force suppression. Actin disruption with latrunculin-A was associated with higher crossbridge phosphorylation when compared with tissues without actin disruption. Shortening velocity, noise temperature, hysteresivity, and stiffness did not differ with and without actin disruption. These data suggest that actin disruption interferes with regulation of crossbridge cycling by crossbridge phosphorylation. Stiffness was linearly dependent on stress, suggesting that the force per attached crossbridge was not altered with force suppression or actin disruption. These data suggest a difference in the mechanical characteristics observed during force suppression and actin disruption, implying that force suppression does not mechanistically involve actin disruption. These data are most consistent with a model where force suppression involves the inhibition of phosphorylated crossbridge binding to thin filaments.
环核苷酸可使动脉平滑肌舒张,而不降低横桥磷酸化水平,这一过程称为力抑制。力抑制有两种潜在机制:1)与细肌丝结合的磷酸化横桥可能受到抑制,或2)细肌丝与锚定结构的附着可能被破坏。通过比较组胺刺激的猪动脉平滑肌在有或没有福斯可林诱导的力抑制以及有或没有拉春库林 - A诱导的肌动蛋白丝破坏的情况下,对这些机制进行了评估。在匹配的力下,与没有力抑制的组织相比,力抑制与低负荷下更高的横桥磷酸化水平和缩短速度相关。高负荷下的缩短速度、噪声温度、滞后性和刚度在有无力抑制的情况下没有差异。这些数据表明,在力抑制过程中,横桥磷酸化调节横桥循环。与没有肌动蛋白破坏的组织相比,拉春库林 - A引起的肌动蛋白破坏与更高的横桥磷酸化水平相关。缩短速度、噪声温度、滞后性和刚度在有无肌动蛋白破坏的情况下没有差异。这些数据表明,肌动蛋白破坏干扰了横桥磷酸化对横桥循环的调节。刚度与应力呈线性相关,表明每个附着横桥的力在力抑制或肌动蛋白破坏时没有改变。这些数据表明在力抑制和肌动蛋白破坏过程中观察到的力学特性存在差异,这意味着力抑制在机制上不涉及肌动蛋白破坏。这些数据与力抑制涉及抑制磷酸化横桥与细肌丝结合的模型最为一致。