Characterization of Slow Wave Activity in Ex-vivo Porcine Small Intestine Segments

Author(s):  
Nipuni D. Nagahawatte ◽  
Niranchan Paskaranandavadivel ◽  
Leo K. Cheng
2019 ◽  
Vol 156 (6) ◽  
pp. S-276
Author(s):  
Wenchang Zhao ◽  
Leonid Ermilov ◽  
Amelia Mazzone ◽  
Jose M. Silva ◽  
Seth T. Eisenman ◽  
...  

2006 ◽  
Vol 242 (2) ◽  
pp. 356-362 ◽  
Author(s):  
Anita Shu-Han Lin ◽  
Martin L. Buist ◽  
Nicolas P. Smith ◽  
Andrew J. Pullan

2013 ◽  
Vol 19 (2) ◽  
pp. 179-191 ◽  
Author(s):  
Timothy R Angeli ◽  
Gregory O'Grady ◽  
Niranchan Paskaranandavadivel ◽  
Jonathan C Erickson ◽  
Peng Du ◽  
...  

1975 ◽  
Vol 229 (2) ◽  
pp. 384-388 ◽  
Author(s):  
BH Brown ◽  
HL Duthie ◽  
AR Horn ◽  
RH Smallwood

The electrical slow-wave activity of the human small intestine has been simulated by a chain of 64 coupled electronic relaxation oscillators. The model simulates the frequency gradient of recorded patoentials in the human small intestine and when transected, behaves in a similar way to the transected canine small intestine. The model exhibits a spontaneous effect whereby several adjacent oscillators periodically are in the same state. This effect travels down the model in the time of 20-30 min.


2014 ◽  
Vol 10 (11) ◽  
pp. e1003923 ◽  
Author(s):  
Arne Weigenand ◽  
Michael Schellenberger Costa ◽  
Hong-Viet Victor Ngo ◽  
Jens Christian Claussen ◽  
Thomas Martinetz

SLEEP ◽  
2017 ◽  
Vol 40 (suppl_1) ◽  
pp. A105-A105
Author(s):  
G Garcia-Molina ◽  
K Baehr ◽  
B Steele ◽  
T Tsoneva ◽  
S Pfundtner ◽  
...  

2009 ◽  
Vol 136 (5) ◽  
pp. A-643
Author(s):  
Juliana H. Kim ◽  
Leonard A. Bradshaw ◽  
Andrew J. Pullan ◽  
Leo K. Cheng

2015 ◽  
Vol 60 (12) ◽  
pp. 3579-3589 ◽  
Author(s):  
Sandeep B. Subramanya ◽  
Betty Stephen ◽  
Soumya S. Nair ◽  
Karl-Herbert Schäfer ◽  
Wim J. Lammers

2015 ◽  
Vol 309 (6) ◽  
pp. C403-C414 ◽  
Author(s):  
Jan D. Huizinga ◽  
Sean P. Parsons ◽  
Ji-Hong Chen ◽  
Andrew Pawelka ◽  
Marc Pistilli ◽  
...  

Phase-amplitude coupling of two pacemaker activities of the small intestine, the omnipresent slow wave activity generated by interstitial cells of Cajal of the myenteric plexus (ICC-MP) and the stimulus-dependent rhythmic transient depolarizations generated by ICC of the deep muscular plexus (ICC-DMP), was recently hypothesized to underlie the orchestration of the segmentation motor pattern. The aim of the present study was to increase our understanding of phase-amplitude coupling through modeling. In particular the importance of propagation velocity of the ICC-DMP component was investigated. The outcome of the modeling was compared with motor patterns recorded from the rat or mouse intestine from which propagation velocities within the different patterns were measured. The results show that the classical segmentation motor pattern occurs when the ICC-DMP component has a low propagation velocity (<0.05 cm/s). When the ICC-DMP component has a propagation velocity in the same order of magnitude as that of the slow wave activity (∼1 cm/s), cluster type propulsive activity occurs which is in fact the dominant propulsive activity of the intestine. Hence, the only difference between the generation of propagating cluster contractions and the Cannon-type segmentation motor pattern is the propagation velocity of the low-frequency component, the rhythmic transient depolarizations originating from the ICC-DMP. Importantly, the proposed mechanism explains why both motor patterns have distinct rhythmic waxing and waning of the amplitude of contractions. The hypothesis is brought forward that the velocity is modulated by neural regulation of gap junction conductance within the ICC-DMP network.


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