Kuizenga Merel H, Sia Tiong C, Dodds Kelsi N, Wiklendt Lukasz, Arkwright John W, Thomas A, Brookes Simon J, Spencer Nick J, Wattchow David A, Dinning Phil G, Costa Marcello
Discipline of Human Physiology, Flinders University, Adelaide, South Australia, Australia;
Discipline of Computer Science, Engineering and Mathematics, Flinders University, Adelaide, South Australia, Australia;
Am J Physiol Gastrointest Liver Physiol. 2015 Jan 1;308(1):G1-G11. doi: 10.1152/ajpgi.00230.2014. Epub 2014 Nov 13.
Narrow muscle strips have been extensively used to study intestinal contractility. Larger specimens from laboratory animals have provided detailed understanding of mechanisms that underlie patterned intestinal motility. Despite progress in animal tissue, investigations of motor patterns in large, intact specimens of human gut ex vivo have been sparse. In this study, we tested whether neurally dependent motor patterns could be detected in isolated specimens of intact human ileum. Specimens (n = 14; 7-30 cm long) of terminal ileum were obtained with prior informed consent from patients undergoing colonic surgery for removal of carcinomas. Preparations were set up in an organ bath with an array of force transducers, a fiberoptic manometry catheter, and a video camera. Spontaneous and distension-evoked motor activity was recorded, and the effects of lidocaine, which inhibits neural activity, were studied. Myogenic contractions (ripples) occurred in all preparations (6.17 ± 0.36/min). They were of low amplitude and formed complex patterns by colliding and propagating in both directions along the specimen at anterograde velocities of 4.1 ± 0.3 mm/s and retrogradely at 4.9 ± 0.6 mm/s. In five specimens, larger amplitude clusters of contractions were seen (discrete clustered contractions), which propagated aborally at 1.05 ± 0.13 mm/s and orally at 1.07 ± 0.09 mm/s. These consisted of two to eight phasic contractions that aligned with ripples. These motor patterns were abolished by addition of lidocaine (0.3 mM). The ripples continued unchanged in the presence of this neural blocking agent. These results demonstrate that both myogenic and neurogenic motor patterns can be studied in isolated specimens of human small intestine.
狭窄的肌肉条带已被广泛用于研究肠道收缩性。来自实验动物的较大标本为理解肠道节律性运动的潜在机制提供了详细信息。尽管在动物组织研究方面取得了进展,但对完整的人体肠道大标本的运动模式进行离体研究却很少。在本研究中,我们测试了在完整的人回肠离体标本中是否能检测到神经依赖性运动模式。从因结肠癌接受结肠手术的患者处获得末端回肠标本(n = 14;长7 - 30 cm),获取标本前已获得患者的知情同意。将标本置于装有一系列力传感器、光纤测压导管和摄像机的器官浴槽中。记录自发的和扩张诱发的运动活动,并研究抑制神经活动的利多卡因的作用。所有标本均出现肌源性收缩(波动)(6.17±0.36次/分钟)。它们振幅较低,通过在标本上双向碰撞和传播形成复杂模式,顺行速度为4.1±0.3 mm/s,逆行速度为4.9±0.6 mm/s。在五个标本中,观察到振幅较大的收缩簇(离散的成簇收缩),其向口端传播速度为1.07±0.09 mm/s,向肛端传播速度为1.05±0.13 mm/s。这些收缩簇由两到八个与波动同步的阶段性收缩组成。添加利多卡因(0.3 mM)后,这些运动模式消失。在这种神经阻断剂存在的情况下,波动持续不变。这些结果表明,在人小肠离体标本中可以研究肌源性和神经源性运动模式。