Chaudhury Arun
GIM Foundation, Little Rock, Arkansas
Am J Physiol Cell Physiol. 2016 Sep 1;311(3):C479-81. doi: 10.1152/ajpcell.00067.2016. Epub 2016 Jul 6.
The gut, a muscular organ, performs a critical role in transporting ingested contents, yet it is also controlled to periodically stop transport to maximize digestion and toxin detection. The complex intraluminal composition and rheology challenge the mechanistic requirements of inhibitory neuromuscular neurotransmission. The interstitial cells of Cajal (ICCs)-generated slow wave may tune the promiscuous luminal chemical environment, which prepares the smooth muscle membrane potential for a depolarizing or hyperpolarizing response as needed. Slow waves are abolished during stimulation-induced inhibitory junction potentials (IJPs) due to purinergic-nitrergic tandem neurotransmission. Recent data demonstrating intact IJPs in a genomic knockout of ICCs provide rigorous evidence of the noncontribution of ICCs during evoked neurotransmission. This perspective article discusses the priority areas of investigations in enteric musculomotor transmission, for understanding its near-perfect design for chemical space sensing, as well as diseases in which the luminal transport braking process becomes dysfunctional, leading to delayed gastric emptying or intestinal transit.
肠道是一个肌肉器官,在运输摄入的内容物方面发挥着关键作用,但它也受到控制,会定期停止运输,以最大限度地进行消化和毒素检测。复杂的管腔内成分和流变学对抑制性神经肌肉神经传递的机制要求提出了挑战。 Cajal间质细胞(ICC)产生的慢波可能会调节混杂的管腔化学环境,根据需要使平滑肌膜电位为去极化或超极化反应做好准备。由于嘌呤能 - 一氧化氮能串联神经传递,在刺激诱导的抑制性连接电位(IJP)期间慢波会消失。最近的数据表明,在ICC基因敲除模型中IJP完整,这为ICC在诱发神经传递过程中不起作用提供了确凿证据。这篇观点文章讨论了肠道肌肉运动传递研究的优先领域,以了解其在化学空间感知方面近乎完美的设计,以及管腔运输制动过程出现功能障碍导致胃排空延迟或肠道运输延迟的疾病。