Department of Physiology and Cell Biology, Anderson Medical Sciences Building/352, University of Nevada School of Medicine, Reno, NV 89557, USA.
J Physiol. 2010 Feb 1;588(Pt 3):399-421. doi: 10.1113/jphysiol.2009.181172. Epub 2009 Nov 30.
The spontaneous colonic migrating motor complex (CMMC) is a cyclical contractile and electrical event that is the primary motor pattern underlying fecal pellet propulsion along the murine colon. We have combined Ca(2+) imaging with immunohistochemistry to determine the role of different classes of myenteric neurons during the CMMC. Between CMMCs, myenteric neurons usually displayed ongoing but uncoordinated activity. Stroking the mucosa at the oral or anal end of the colon resulted in a CMMC (latency: 6 to 10 s; duration: 28 s) that consisted of prolonged increases in activity in many myenteric neurons that was correlated to Ca(2+) transients in and displacement of the muscle. These neurons were likely excitatory motor neurons. Activity in individual neurons during the CMMC was similar regardless of whether the CMMC occurred spontaneously or was evoked by anal or oral mucosal stimulation. This suggests that convergent interneuronal pathways exist which generate CMMCs. Interestingly, Ca(2+) transients in a subset of NOS +ve neurons were substantially reduced during the CMMC. These neurons are likely to be inhibitory motor neurons that reduce their activity during a complex (disinhibition) to allow full excitation of the muscle. Local stimulation of the mucosa evoked synchronized Ca(2+) transients in Dogiel Type II (mitotracker/calbindin-positive) neurons after a short delay (1-2 s), indicating they were the sensory neurons underlying the CMMC. These local responses were observed in hexamethonium, but were blocked by ondansetron (5-HT(3) antagonist), suggesting Dogiel Type II neurons were activated by 5-HT release from enterochromaffin cells in the mucosa. In fact, removal of the mucosa yielded no spontaneous CMMCs, although many neurons (NOS +ve and NOS ve) exhibited ongoing activity, including Dogiel Type II neurons. These results suggest that spontaneous or evoked 5-HT release from the mucosa is necessary for the activation of Dogiel Type II neurons that generate CMMCs.
自发性结肠移行性运动复合波(CMMC)是一种周期性收缩和电活动,是推动鼠结肠中粪便颗粒前进的主要运动模式。我们结合钙成像和免疫组织化学来确定不同类型的肌间神经元在 CMMC 期间的作用。在 CMMC 之间,肌间神经元通常表现出持续但不协调的活动。在结肠的口腔或肛门端刷拭黏膜会导致 CMMC(潜伏期:6 至 10 秒;持续时间:28 秒),该 CMMC 由许多肌间神经元的活动延长增加组成,与肌肉内的钙瞬变和位移相关。这些神经元可能是兴奋性运动神经元。CMMC 期间单个神经元的活动相似,无论 CMMC 是否自发发生还是由肛门或口腔黏膜刺激诱发。这表明存在会聚的中间神经元途径,这些途径会产生 CMMC。有趣的是,在 CMMC 期间,一组 NOS +ve 神经元的钙瞬变明显减少。这些神经元可能是抑制性运动神经元,它们在复杂过程中降低其活动(去抑制)以允许肌肉充分兴奋。黏膜的局部刺激会在短延迟(1-2 秒)后诱发 Dogiel 型 II(mitotracker/calbindin 阳性)神经元的同步钙瞬变,表明它们是 CMMC 的基础感觉神经元。这些局部反应在六烃季铵存在下观察到,但被昂丹司琼(5-HT3 拮抗剂)阻断,表明 Dogiel 型 II 神经元是由黏膜内肠嗜铬细胞释放的 5-HT 激活的。事实上,去除黏膜不会产生自发的 CMMC,但许多神经元(NOS +ve 和 NOS ve)表现出持续的活动,包括 Dogiel 型 II 神经元。这些结果表明,黏膜中自发或诱发的 5-HT 释放对于激活产生 CMMC 的 Dogiel 型 II 神经元是必要的。