Intrinsic primary afferent neurons and nerve circuits within the intestine

被引:262
作者
Furness, JB [1 ]
Jones, C
Nurgali, K
Clerc, N
机构
[1] Univ Melbourne, Dept Anat & Cell Biol, Parkville, Vic 3010, Australia
[2] Univ Melbourne, Ctr Neurosci, Parkville, Vic 3010, Australia
[3] Univ Mediterranee, CNRS, UMR, Lab ITIS, Marseille, France
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.pneurobio.2003.12.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Intrinsic primary afferent neurons (IPANs) of the enteric nervous system are quite different from all other peripheral neurons. The IPANs are transducers of physiological stimuli, including movement of the villi or distortion of the mucosa, contraction of intestinal muscle and changes in the chemistry of the contents of the gut lumen. They are the first neurons in intrinsic reflexes that influence the patterns of motility, secretion of fluid across the mucosal epithelium and local blood flow in the small and large intestines. In the guinea pig small intestine, where they have been characterized in detail, IPANs have Dogiel type II morphology, that is they are large round or oval neurons with multiple processes, some of which end close to the luminal surface of the intestine, and some of which form synapses with enteric interneurons, motor neurons and with other IPANs. The IPANs have well-defined ionic currents through which their excitability, and their functions in enteric nerve circuits, is determined. These include voltage-gated Na+ and Ca2+ currents, a long lasting calcium-activated K+ current, and a hyperpolarization-activated cationic current. The IPANs exhibit long-term changes in their states of excitation that can be induced by extended periods of low frequency activity in synaptic inputs and by inflammatory mediators, either applied directly or released during an inflammatory challenge. The IPANs may be involved in pathological changes in enteric function following inflammation. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:143 / 164
页数:22
相关论文
共 195 条
[1]   A new model of chronic visceral hypersensitivity in adult rats induced by colon irritation during postnatal development [J].
Al-Chaer, ED ;
Kawasaki, M ;
Pasricha, PJ .
GASTROENTEROLOGY, 2000, 119 (05) :1276-1285
[2]   Responses of myenteric S neurones to low frequency stimulation of their synaptic inputs [J].
Alex, G ;
Clerc, N ;
Kunze, WAA ;
Furness, JB .
NEUROSCIENCE, 2002, 110 (02) :361-373
[3]   Comparison of the effects of neurokinin-3 receptor blockade on two forms of slow synaptic transmission in myenteric AH neurons [J].
Alex, G ;
Kunze, WAA ;
Furness, JB ;
Clerc, N .
NEUROSCIENCE, 2001, 104 (01) :263-269
[4]  
[Anonymous], TXB PHYSL
[5]  
[Anonymous], AUTONOMIC NERVOUS SY
[6]  
BALDWIN M V, 1975, P75
[7]   Role of immunologic factors and cyclooxygenase 2 in persistent postinfective enteric muscle dysfunction in mice [J].
Barbara, G ;
De Giorgio, R ;
Deng, YK ;
Vallance, B ;
Blennerhassett, P ;
Collins, SM .
GASTROENTEROLOGY, 2001, 120 (07) :1729-1736
[8]   Persistent intestinal neuromuscular dysfunction after acute nematode infection in mice [J].
Barbara, G ;
Vallance, BA ;
Collins, SM .
GASTROENTEROLOGY, 1997, 113 (04) :1224-1232
[9]  
Bayliss W M, 1899, J Physiol, V24, P99
[10]   The terminals of myenteric intrinsic primary afferent neurons of the guinea-pig ileum are excited by 5-hydroxytryptamine acting at 5-hydroxytryptamine-3 receptors [J].
Bertrand, PP ;
Kunze, WAA ;
Furness, JB ;
Bornstein, JC .
NEUROSCIENCE, 2000, 101 (02) :459-469