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肠道神经反射对Ca2+波的诱导与组织

Induction and organization of Ca2+ waves by enteric neural reflexes.

作者信息

Stevens R J, Publicover N G, Smith T K

机构信息

Biomedical Engineering Program and Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno 89557, USA.

出版信息

Nature. 1999 May 6;399(6731):62-6. doi: 10.1038/19973.

Abstract

The motility of the gastrointestinal tract consists of local, non-propulsive mixing (pendular or segmental) and propulsive (peristaltic) movements. It is generally considered that mixing movements are produced by intrinsic pacemakers which generate rhythmic contractions, and peristalsis by intrinsic excitatory and inhibitory neural reflex pathways, but the relationship between mixing and peristalsis is poorly understood. Peristalsis is compromised in mice lacking interstitial cells of Cajal, suggesting that these pacemaker cells may also be involved in neural reflexes. Here we show that mixing movements within longitudinal muscle result from spontaneously generated waves of elevated internal calcium concentration which originate from discrete locations (pacing sites), spread with anisotropic conduction velocities in al directions, and terminate by colliding with each other or with adjacent neurally suppressed regions. Excitatory neural reflexes control the spread of excitability by inducing new pacing sites and enhancing the overall frequency of pacing, whereas inhibitory reflexes suppress the ability of calcium waves to propagate. We provide evidence that the enteric nervous system organizes mixing movements to generate peristalsis, linking the neural regulation of pacemakers to both types of gut motility.

摘要

胃肠道的运动由局部非推进性混合运动(钟摆样或节段性运动)和推进性(蠕动)运动组成。一般认为,混合运动由产生节律性收缩的内在起搏器产生,蠕动则由内在的兴奋性和抑制性神经反射通路产生,但混合运动与蠕动之间的关系仍知之甚少。在缺乏 Cajal 间质细胞的小鼠中,蠕动功能受损,这表明这些起搏细胞可能也参与神经反射。在此我们表明,纵行肌内的混合运动源于内部钙浓度升高的自发波,这些波起源于离散位置(起搏点),以各向异性传导速度向各个方向传播,并通过相互碰撞或与相邻的神经抑制区域碰撞而终止。兴奋性神经反射通过诱导新的起搏点和提高整体起搏频率来控制兴奋性的传播,而抑制性反射则抑制钙波的传播能力。我们提供的证据表明,肠神经系统组织混合运动以产生蠕动,将起搏器的神经调节与两种类型的肠道运动联系起来。

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