Literature DB >> 11146431

Consequences of intestinal inflammation on the enteric nervous system: neuronal activation induced by inflammatory mediators.

K A Sharkey1, A B Kroese.   

Abstract

The ENS is responsible for the regulation and control of all gastrointestinal functions. Because of this critical role, and probably as a consequence of its remarkable plasticity, the ENS is often relatively well preserved in conditions where the architecture of the intestine is seriously disrupted, such as in IBD. There are structural and functional changes in the enteric innervation in animal models of experimental intestinal inflammation and in IBD. These include both up and down regulation of transmitter expression and the induction of new genes in enteric neurons. Using Fos expression as a surrogate marker of neuronal activation it is now well established that enteric neurons (and also enteric glia) respond to inflammation. Whether this "activation" is limited to a short-term functional response, such as increased neuronal excitability, or reflects a long-term change in some aspect of the neuronal phenotype (or both) has yet to be firmly established, but it appears that enteric neurons are highly plastic in their response to inflammation. Copyright 2001 Wiley-Liss, Inc.

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Year:  2001        PMID: 11146431     DOI: 10.1002/1097-0185(20010101)262:1<79::AID-AR1013>3.0.CO;2-K

Source DB:  PubMed          Journal:  Anat Rec        ISSN: 0003-276X


  36 in total

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4.  Differential effects of experimental ulcerative colitis on P2X7 receptor expression in enteric neurons.

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5.  Role of the A(2B) receptor-adenosine deaminase complex in colonic dysmotility associated with bowel inflammation in rats.

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6.  Bioengineered three-dimensional physiological model of colonic longitudinal smooth muscle in vitro.

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7.  Structural changes in the epithelium of the small intestine and immune cell infiltration of enteric ganglia following acute mucosal damage and local inflammation.

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Review 9.  Enteric P2X receptors as potential targets for drug treatment of the irritable bowel syndrome.

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10.  Effect of selective inhibition of monoacylglycerol lipase (MAGL) on acute nausea, anticipatory nausea, and vomiting in rats and Suncus murinus.

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