Literature DB >> 17598957

Mechanism of abnormal intestinal motility in inflammatory bowel disease: how smooth muscle contraction is reduced?

Takashi Ohama1, Masatoshi Hori, Hiroshi Ozaki.   

Abstract

Intestinal inflammation alters the contractile activity of intestinal smooth muscle. Motility disorders of the gastrointestinal tract are clinically important symptoms, because they are often associated with severe interstitial inflammation. In addition, the motility disorders secondarily induce abnormal growth of the intestinal flora, and the resulting disturbance of this flora aggravates the pathogenesis of mucosal inflammation. This in turn aggravates the intestinal dysmotility; i.e., it is an inflammatory spiral. Therefore, it is important to elucidate the mechanisms involved in the changes in motor function which occur in intestinal inflammation. Recent studies have revealed several molecular mechanisms responsible for the decreased motility which occurs in an inflamed gastrointestinal tract. In the present review, we discuss the functional failure of smooth muscle cells, including changes in the activity of muscarinic receptors, ion channels and the endogenous myosin phosphatase inhibitor CPI-17.

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Mesh:

Year:  2007        PMID: 17598957     DOI: 10.1540/jsmr.43.43

Source DB:  PubMed          Journal:  J Smooth Muscle Res        ISSN: 0916-8737


  29 in total

1.  Inhibitory effect of cannabichromene, a major non-psychotropic cannabinoid extracted from Cannabis sativa, on inflammation-induced hypermotility in mice.

Authors:  Angelo A Izzo; Raffaele Capasso; Gabriella Aviello; Francesca Borrelli; Barbara Romano; Fabiana Piscitelli; Laura Gallo; Francesco Capasso; Pierangelo Orlando; Vincenzo Di Marzo
Journal:  Br J Pharmacol       Date:  2012-06       Impact factor: 8.739

Review 2.  Current view of the immunopathogenesis in inflammatory bowel disease and its implications for therapy.

Authors:  M-I Torres; A Rios
Journal:  World J Gastroenterol       Date:  2008-04-07       Impact factor: 5.742

3.  Contribution of Rho-kinase to membrane excitability of murine colonic smooth muscle.

Authors:  O Bayguinov; L Dwyer; H Kim; A Marklew; K M Sanders; S D Koh
Journal:  Br J Pharmacol       Date:  2011-06       Impact factor: 8.739

4.  MAPKs represent novel therapeutic targets for gastrointestinal motility disorders.

Authors:  Eikichi Ihara; Hirotada Akiho; Kazuhiko Nakamura; Sara R Turner; Justin A Macdonald
Journal:  World J Gastrointest Pathophysiol       Date:  2011-04-15

5.  In vivo roles for myosin phosphatase targeting subunit-1 phosphorylation sites T694 and T852 in bladder smooth muscle contraction.

Authors:  Cai-Ping Chen; Xin Chen; Yan-Ning Qiao; Pei Wang; Wei-Qi He; Cheng-Hai Zhang; Wei Zhao; Yun-Qian Gao; Chen Chen; Tao Tao; Jie Sun; Ye Wang; Ning Gao; Kristine E Kamm; James T Stull; Min-Sheng Zhu
Journal:  J Physiol       Date:  2014-12-23       Impact factor: 5.182

6.  Cytokine-induced S-nitrosylation of soluble guanylyl cyclase and expression of phosphodiesterase 1A contribute to dysfunction of longitudinal smooth muscle relaxation.

Authors:  Senthilkumar Rajagopal; Ancy D Nalli; Divya P Kumar; Sayak Bhattacharya; Wenhui Hu; Sunila Mahavadi; John R Grider; Karnam S Murthy
Journal:  J Pharmacol Exp Ther       Date:  2014-12-30       Impact factor: 4.030

Review 7.  Mechanisms of smooth muscle responses to inflammation.

Authors:  T Shea-Donohue; L Notari; R Sun; A Zhao
Journal:  Neurogastroenterol Motil       Date:  2012-09       Impact factor: 3.598

8.  Upregulation of RGS4 and downregulation of CPI-17 mediate inhibition of colonic muscle contraction by interleukin-1beta.

Authors:  Wenhui Hu; Sunila Mahavadi; Fang Li; Karnam S Murthy
Journal:  Am J Physiol Cell Physiol       Date:  2007-10-24       Impact factor: 4.249

9.  Cannabidiol, extracted from Cannabis sativa, selectively inhibits inflammatory hypermotility in mice.

Authors:  R Capasso; F Borrelli; G Aviello; B Romano; C Scalisi; F Capasso; A A Izzo
Journal:  Br J Pharmacol       Date:  2008-05-12       Impact factor: 8.739

10.  Cytokine-induced iNOS and ERK1/2 inhibit adenylyl cyclase type 5/6 activity and stimulate phosphodiesterase 4D5 activity in intestinal longitudinal smooth muscle.

Authors:  Sunila Mahavadi; Ancy D Nalli; Divya P Kumar; Wenhui Hu; John F Kuemmerle; John R Grider; Karnam S Murthy
Journal:  Am J Physiol Cell Physiol       Date:  2014-06-18       Impact factor: 4.249

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