Literature DB >> 12213103

Anisotropic propagation in the small intestine.

W J E P Lammers1, B Stephen, J R Slack, S Dhanasekaran.   

Abstract

Abstract Measuring propagation anisotropy may help in determining the tissue layers involved in the propagation of electrical impulses in the intestine. We used 240 extracellular electrograms recorded from the isolated feline duodenum. The conduction velocities of slow waves and of individual spikes were measured from their site of origin into all directions. Both slow waves and spikes propagate anisotropically in the small intestine but in different directions and to a different degree. Slow waves propagated anisotropically faster in the circumferential (1.7 +/- 0.8 cm s(-1)) than in the axial direction (1.3 +/- 0.5 cm s(-1); P < 0.001). Spikes, on the other hand, propagated faster in the longitudinal direction (7.8 +/- 4.5 cm s(-1)) than in the circumferential direction (3.3 +/- 4.3 cm s(-1); P < 0.001). Furthermore, the average conduction velocity of spikes (6.3 +/- 4.5 cm s(-1)) was significantly higher than that of slow waves (1.5 +/- 1.1 cm s(-1); P < 0.001). The anisotropic propagation of spikes supports the argument that these propagate in the longitudinal muscle layer. The anisotropic propagation of slow waves may be the result of the interaction between the myenteric layer of interstitial cells of Cajal and their electrotonic connection to both the longitudinal and the circular muscle layer.

Mesh:

Year:  2002        PMID: 12213103     DOI: 10.1046/j.1365-2982.2002.00340.x

Source DB:  PubMed          Journal:  Neurogastroenterol Motil        ISSN: 1350-1925            Impact factor:   3.598


  12 in total

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2.  Enteric sensory neurons communicate with interstitial cells of Cajal to affect pacemaker activity in the small intestine.

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3.  Motor patterns of the small intestine explained by phase-amplitude coupling of two pacemaker activities: the critical importance of propagation velocity.

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4.  Rapid high-amplitude circumferential slow wave propagation during normal gastric pacemaking and dysrhythmias.

Authors:  G O'Grady; P Du; N Paskaranandavadivel; T R Angeli; W J E P Lammers; S J Asirvatham; J A Windsor; G Farrugia; A J Pullan; L K Cheng
Journal:  Neurogastroenterol Motil       Date:  2012-07       Impact factor: 3.598

5.  Detailed measurements of gastric electrical activity and their implications on inverse solutions.

Authors:  Leo K Cheng; Greg O'Grady; Peng Du; John U Egbuji; John A Windsor; Andrew J Pullan
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6.  Circumferential and functional re-entry of in vivo slow-wave activity in the porcine small intestine.

Authors:  T R Angeli; G O'Grady; P Du; N Paskaranandavadivel; A J Pullan; I P Bissett; L K Cheng
Journal:  Neurogastroenterol Motil       Date:  2013-03-12       Impact factor: 3.598

Review 7.  The virtual intestine: in silico modeling of small intestinal electrophysiology and motility and the applications.

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8.  Iterative Covariance-Based Removal of Time-Synchronous Artifacts: Application to Gastrointestinal Electrical Recordings.

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9.  The gastrointestinal electrical mapping suite (GEMS): software for analyzing and visualizing high-resolution (multi-electrode) recordings in spatiotemporal detail.

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Journal:  BMC Gastroenterol       Date:  2012-06-06       Impact factor: 3.067

10.  Experimental and Automated Analysis Techniques for High-resolution Electrical Mapping of Small Intestine Slow Wave Activity.

Authors:  Timothy R Angeli; Gregory O'Grady; Niranchan Paskaranandavadivel; Jonathan C Erickson; Peng Du; Andrew J Pullan; Ian P Bissett; Leo K Cheng
Journal:  J Neurogastroenterol Motil       Date:  2013-04-16       Impact factor: 4.924

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