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刺激史会影响大鼠肠系膜小动脉的血管舒缩反应。

Stimulation history affects vasomotor responses in rat mesenteric arterioles.

机构信息

Department of Neuroscience, University of Copenhagen, Copenhagen, Denmark.

Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.

出版信息

Pflugers Arch. 2019 Feb;471(2):271-283. doi: 10.1007/s00424-018-2206-0. Epub 2018 Sep 15.

DOI:10.1007/s00424-018-2206-0
PMID:30219946
Abstract

Resistance vessels regulate blood flow by continuously adjusting activity of the wall smooth muscle cells. These cells integrate a variety of stimuli from blood, endothelium, autonomic nerves, and surrounding tissues. Each stimulus elicits an intracellular signaling cascade that eventually influences activation of the contractile machinery. The characteristic time scale of each cascade and the sharing of specific reactions between cascades provide for complex behavior when a vessel receives multiple stimuli. Here, we apply sequential stimulation with invariant concentrations of vasoconstrictor (norepinephrine/methoxamine) and vasodilator (SNAP/carbacol) to rat mesenteric vessels in the wire myograph to show that (1) time elapsed between addition of two vasoactive drugs and (2) the sequence of addition may significantly affect final force development. Furthermore, force oscillations (vasomotion) often appear upon norepinephrine administration. Using computational modeling in combination with nitric oxide (NO) inhibition/NO addition experiments, we show that (3) amplitude and number of oscillating vessels increase over time, (4) the ability of NO to induce vasomotion depends on whether it is applied before or after norepinephrine, and (5) emergence of vasomotion depends on the prior dynamical state of the system; in simulations, this phenomenon appears as "hysteresis." These findings underscore the time-dependent nature of vascular tone generation which must be considered when evaluating the vasomotor effects of multiple, simultaneous stimuli in vitro or in vivo.

摘要

阻力血管通过不断调整血管平滑肌细胞的活动来调节血流量。这些细胞整合了来自血液、内皮、自主神经和周围组织的各种刺激。每种刺激都会引发细胞内信号级联反应,最终影响收缩机制的激活。每个级联的特征时间尺度和级联之间特定反应的共享为血管接受多种刺激时提供了复杂的行为。在这里,我们应用具有不变浓度的血管收缩剂(去甲肾上腺素/甲氧胺)和血管扩张剂(SNAP/ carbacol)的顺序刺激,在钢丝肌动描记器中研究大鼠肠系膜血管,以表明(1)两种血管活性药物添加之间的时间间隔,以及(2)添加的顺序可能会显著影响最终的力发展。此外,在去甲肾上腺素给药时经常会出现力振荡(血管运动)。通过使用计算建模与一氧化氮(NO)抑制/NO 添加实验相结合,我们表明(3)随着时间的推移,振荡血管的幅度和数量增加,(4)NO 诱导血管运动的能力取决于它是在去甲肾上腺素之前还是之后应用,以及(5)血管运动的出现取决于系统的先前动力学状态;在模拟中,这种现象表现为“滞后”。这些发现强调了血管张力产生的时间依赖性,在评估体外或体内多种同时刺激的血管运动效应时必须考虑到这一点。

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本文引用的文献

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Differential α-adrenergic modulation of rapid onset vasodilatation along resistance networks of skeletal muscle in old versus young mice.老年小鼠与年轻小鼠骨骼肌阻力网络中快速起效血管舒张的差异性α-肾上腺素能调节
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Inefficient functional sympatholysis is an overlooked cause of malperfusion in contracting skeletal muscle.
收缩期骨骼肌灌注不良的一个被忽视的原因是功能性交感神经松弛作用效率低下。
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Sympathetic nerve stimulation induces local endothelial Ca2+ signals to oppose vasoconstriction of mouse mesenteric arteries.交感神经刺激诱导局部内皮细胞 Ca2+ 信号,拮抗小鼠肠系膜动脉的血管收缩。
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Bestrophin is important for the rhythmic but not the tonic contraction in rat mesenteric small arteries.Bestrophin 对于大鼠肠系膜小动脉的节律性收缩而非紧张性收缩很重要。
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Role of myosin light chain kinase and myosin light chain phosphatase in the resistance arterial myogenic response to intravascular pressure.肌球蛋白轻链激酶和肌球蛋白轻链磷酸酶在抵抗血管内压的动脉肌源性反应中的作用。
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Heterogeneity and weak coupling may explain the synchronization characteristics of cells in the arterial wall.异质性和弱耦合可能解释动脉壁中细胞的同步特性。
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9
Stability of norepinephrine infusions prepared in dextrose and normal saline solutions.在葡萄糖溶液和生理盐水中制备的去甲肾上腺素输注液的稳定性。
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10
Activation of a cGMP-sensitive calcium-dependent chloride channel may cause transition from calcium waves to whole cell oscillations in smooth muscle cells.环磷酸鸟苷(cGMP)敏感性钙依赖性氯通道的激活可能导致平滑肌细胞中从钙波向全细胞振荡的转变。
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