Spencer N J, Smith C B, Smith T K
Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, USA.
J Physiol. 2001 Jan 15;530(Pt 2):295-306. doi: 10.1111/j.1469-7793.2001.0295l.x.
We investigated the involvement of muscle tone and circular muscle (CM) contraction in peristalsis in isolated guinea-pig small intestine. A segment of jejunum (approximately 13 cm) was mounted into a three chambered partitioned bath. Peristaltic waves were initiated in the oral chamber either by: (1) infusing fluid into the oral end of the jejunum; the ejected fluid was diverted via a cannula from reaching the intermediate and anal chambers, or by (2) intraluminal balloon distension of the empty oral segment. Tension of the circular muscle was measured in all three chambers. Peristaltic waves elicited by fluid infusion were evoked at an abrupt threshold. In contrast, peristaltic waves elicited by distension could be graded in amplitude according to stimulus intensity. Peristaltic waves evoked in an empty intestine exhibited similar propagation velocities to peristaltic waves associated with fluid propulsion. Nifedipine (200-400 nM) added to the intermediate chamber to block muscle contraction did not prevent peristaltic waves elicited by either stimulus from propagating into the anal chamber, although their amplitude was attenuated. Nifedipine to the site of stimulation (oral chamber) abolished peristaltic waves generated by either stimulus. Tetrodotoxin (1-2 microM), or a low Ca2+-high Mg2+ solution to the intermediate chamber abolished the propagation of peristalsis from the oral to anal chambers. In conclusion, graded peristaltic waves can occur in an empty intestine. Therefore peristalsis is not necessarily an "all-or-none" phenomenon. Peristalsis depends on the spread of nervous activity along the bowel, rather than the reactivation of neural circuits caused by displacement of fluid in the lumen. However, local muscle tone and contraction are important for the initiation and maintenance of peristaltic propagation.
我们研究了肌张力和环行肌(CM)收缩在豚鼠离体小肠蠕动中的作用。将一段空肠(约13厘米)安装到三室分隔浴槽中。蠕动波可通过以下方式在口腔端腔室引发:(1)向空肠口腔端注入液体;喷出的液体通过插管引流,使其无法到达中间腔室和肛门腔室;或者(2)对空的口腔段进行腔内球囊扩张。在所有三个腔室中测量环行肌的张力。液体注入引发的蠕动波在一个突然的阈值下诱发。相比之下,扩张引发的蠕动波其幅度可根据刺激强度分级。在空肠中诱发的蠕动波与液体推进相关的蠕动波表现出相似的传播速度。添加到中间腔室以阻断肌肉收缩的硝苯地平(200 - 400 nM)并不能阻止由任何一种刺激引发的蠕动波传播到肛门腔室,尽管其幅度有所衰减。在刺激部位(口腔端腔室)加入硝苯地平可消除由任何一种刺激产生的蠕动波。在中间腔室加入河豚毒素(1 - 2 microM)或低钙 - 高镁溶液可消除蠕动从口腔端腔室向肛门腔室的传播。总之,分级蠕动波可在空肠中发生。因此,蠕动不一定是一种“全或无”现象。蠕动依赖于神经活动沿肠道的传播,而不是由肠腔内液体位移引起的神经回路的重新激活。然而,局部肌张力和收缩对于蠕动传播的起始和维持很重要。