Enteric nervous system: sensory physiology, diarrhea and constipation

被引:52
作者
Wood, Jackie D. [1 ,2 ]
机构
[1] Ohio State Univ, Coll Med, Dept Physiol & Cell Biol, Columbus, OH 43210 USA
[2] Ohio State Univ, Coll Med, Dept Internal Med, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
angiotensin II; CFTR channels; ClC-2; channels; dorsal root ganglia; lubiprostone; mechanoreceptors; prostaglandins; secretomotor neurons; PRIMARY AFFERENT NEURONS; INTRAGANGLIONIC LAMINAR ENDINGS; VAGAL TENSION RECEPTORS; ACTIVATED MAST-CELLS; SMALL-INTESTINE; SYNAPTIC-TRANSMISSION; ELECTRICAL-ACTIVITY; CHLORIDE CHANNELS; EPITHELIAL-CELLS; LUBIPROSTONE;
D O I
10.1097/MOG.0b013e328334df4f
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Purpose of review The enteric nervous system integrates secretion and motility into homeostatic patterns of behavior susceptible to disorder. Progress in understanding mechanosensory detection in these processes, disordered enteric nervous system integration in diarrhea and constipation and pharmacotherapy is summarized. Recent findings Most neurons in the enteric nervous system discharge in response to distortion. Drugs acting directly to open chloride conductance channels in the mucosal epithelium are therapeutic options for constipation. Summary Mechanoreception is required for negative feedback control. At issue is identification of the neurons that fulfil the requirement for mechanoreception. Understanding secretomotor neurons is basic to understanding neurogenic secretory diarrhea and constipation and therapeutic strategies. A strategy for treatment of chronic constipation is development of agents that act directly to open Cl- channels, which thereby increases the liquidity of the luminal contents. Lubiprostone, a recently Food and Drug Administration-approved drug, increases intraluminal liquidity by opening Cl- channels. The future for the drug is clouded by controversy over whether its action is directly at one or the other of chloride channel type 2 (ClC-2) or cystic fibrosis transmembrane conductance regulator (CFTR) chloride channels or both and whether action reflects involvement of G protein-coupled prostaglandin receptors expressed by mucosal epithelial cells.
引用
收藏
页码:102 / 108
页数:7
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