Rahman Awahan, Matchkov Vladimir, Nilsson Holger, Aalkjaer Christian
The Water and Salt Center, Institute of Physiology and Biophysics, University of Aarhus, Denmark.
J Vasc Res. 2005 Jul-Aug;42(4):301-11. doi: 10.1159/000086002. Epub 2005 May 26.
We tested the hypothesis that cGMP can induce a state of only partial coordination of vascular smooth muscle cells (VSMC).
This was done by studying the concentration-dependent effect of 8Br-cGMP on isometric and isobaric force development of noradrenaline-activated segments of rat mesenteric small arteries in which the endothelium was removed. We further measured the concentration-dependent effect of 8Br-cGMP on VSMC membrane potential, spatially resolved Ca(2+) and VSMC membrane conductance.
With 300 microM 8Br-cGMP, coordinated Ca(2+) activity and vasomotion were seen as previously reported. At 10-30 microM 8Br-cGMP, beating isometric tension oscillations were seen. Isobaric recordings revealed oscillations with different frequencies in different parts of the arteries. At these (10-30 microM) 8Br-cGMP concentrations, membrane potential oscillations did not always concur with isometric tension oscillations, and Ca(2+) oscillations were only synchronized locally within groups of cells. 8Br-cGMP concentration-dependently decreased the frequency of vasomotion and, in unsynchronized hyperpolarized VSMC, the frequency of Ca(2+) waves.
Our results demonstrated that cGMP can cause a partial coordination of the VSMC in the vascular wall (and at high concentrations near complete coordination). Furthermore, the cGMP concentration-dependent decrease of Ca(2+) wave frequency and of vasomotion frequency suggests that cGMP modifies oscillatory Ca(2+) release from the sarcoplasmic reticulum and supports the suggestion that this oscillatory release paces vasomotion.
我们验证了环磷酸鸟苷(cGMP)可诱导血管平滑肌细胞(VSMC)仅部分协调状态的假说。
通过研究8-溴环磷酸鸟苷(8Br-cGMP)对去内皮大鼠肠系膜小动脉去甲肾上腺素激活段等长和等压张力发展的浓度依赖性效应来实现。我们还进一步测量了8Br-cGMP对VSMC膜电位、空间分辨的胞内钙离子浓度(Ca(2+))和VSMC膜电导的浓度依赖性效应。
使用300微摩尔8Br-cGMP时,观察到如先前报道的协调的Ca(2+)活性和血管运动。在10 - 30微摩尔8Br-cGMP时,观察到搏动性等长张力振荡。等压记录显示动脉不同部位有不同频率的振荡。在这些(10 - 30微摩尔)8Br-cGMP浓度下,膜电位振荡并不总是与等长张力振荡同步,且Ca(2+)振荡仅在细胞群内局部同步。8Br-cGMP浓度依赖性地降低血管运动频率,以及在未同步的超极化VSMC中降低Ca(2+)波频率。
我们的结果表明,cGMP可导致血管壁中VSMC的部分协调(在高浓度时接近完全协调)。此外,cGMP浓度依赖性地降低钙离子波频率和血管运动频率表明,cGMP改变了肌浆网中振荡性钙离子释放,并支持这种振荡性释放为血管运动提供节律的观点。