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Vasomotion: cellular background for the oscillator and for the synchronization of smooth muscle cells

机译:血管运动:振荡器和平滑肌细胞同步的细胞背景

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class="enumerated" style="list-style-type:decimal">Vasomotion is the oscillation of vascular tone with frequencies in the range from 1 to 20 min−1 seen in most vascular beds. The oscillation originates in the vessel wall and is seen both in vivo and in vitro.Recently, our ideas on the cellular mechanisms responsible for vasomotion have improved. Three different types of cellular oscillations have been suggested. One model has suggested that oscillatory release of Ca2+ from intracellular stores is important (the oscillation is based on a cytosolic oscillator). A second proposed mechanism is an oscillation originating in the sarcolemma (a membrane oscillator). A third mechanism is based on an oscillation of glycolysis (metabolic oscillator). For the two latter mechanisms, only limited experimental evidence is available.To understand vasomotion, it is important to understand how the cells synchronize. For the cytosolic oscillators synchronization may occur via activation of Ca2+-sensitive ion channels by oscillatory Ca2+ release. The ensuing membrane potential oscillation feeds back on the intracellular Ca2+ stores and causes synchronization of the Ca2+ release. While membrane oscillators in adjacent smooth muscle cells could be synchronized through the same mechanism that sets up the oscillation in the individual cells, a mechanism to synchronize the metabolic-based oscillators has not been suggested.The interpretation of the experimental observations is supported by theoretical modelling of smooth muscle cells behaviour, and the new insight into the mechanisms of vasomotion has the potential to provide tools to investigate the physiological role of vasomotion.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 血管运动是在大多数血管床中可见的频率在1到20 min −1 范围内的血管张力的振荡。振荡起源于血管壁,并在体内和体外均可见。 最近,我们对负责血管运动的细胞机制的观念得到了改善。已经提出了三种不同类型的细胞振荡。一种模型表明,Ca 2 + 从细胞内存储区的振荡释放很重要(振荡基于胞质振荡子)。提出的第二种机制是起源于肌膜(膜振荡器)的振荡。第三种机制是基于糖酵解的振荡(代谢振荡器)。对于后两种机制,只有有限的实验证据。 要了解血管运动,重要的是要了解细胞如何同步。对于胞质振荡器,同步性可能是通过振荡释放Ca 2 + 激活Ca 2 + 敏感离子通道而发生的。随后的膜电位振荡反馈到细胞内Ca 2 + 的存储上,并导致Ca 2 + 释放的同步。虽然可以通过在单个细胞中建立振荡的相同机制来同步相邻平滑肌细胞中的膜振荡子,但尚未提出同步基于代谢物的振荡子的机制。 平滑肌细胞行为的理论模型为实验性观察提供了支持,而对血管运动机制的新见识也有可能为研究血管运动的生理作用提供工具。

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