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Am J Physiol Gastrointest Liver Physiol (October 10, 2001). doi:10.1152/ajpgi.00335.2001
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Articles in PresS, published online ahead of print October 10, 2001
Am J Physiol Gastrointest Liver Physiol, 10.1152/ajpgi.00335.2001
Submitted on August 1, 2001
Accepted on October 9, 2001

Patterns of excitability in human esophageal sensorimotor cortex to painful and non-painful visceral stimulation

Shaheen Hamdy1*, John C Rothwell2, Chris Fraser3, Maxine Power3, David Gow3, and David G Thompson3

1 GI Science, University of Manchester, Salford, Manchester, United Kingdom; Sobell Department of Neurophysiology, Institute of Neurology, London, United Kingdom
2 Sobell Department of Neurophysiology, Institute of Neurology, London, United Kingdom
3 GI Science, University of Manchester, Salford, Manchester, United Kingdom

* To whom correspondence should be addressed. E-mail: shamdy{at}fs1.ho.man.ac.uk.

Background/Aims: To better understand the relationship between cortical plasticity and visceral pain, we developed a pain-induced model of altered esophageal cortico-bulbar excitability. Methods: In 8 healthy volunteers cortico-esophageal EMG responses were recorded via an intra-luminal catheter, following magnetic stimulation of the right sensorimotor cortex using peri-threshold intensities. Cortico-thenar responses were also acquired as control. Responses were assessed both before and for up to 1 hour after either painful or non-painful balloon distension of esophagus (frequency=1 Hz, dwell time=200 ms, duration=10 minutes), each being delivered to each subject in random order. Results: Painful esophageal distension (mean volume=11±3 ml) induced a profound increase in esophageal responses compared to baseline levels (at 30 minutes: 141±22 vs. 91±19 µV, p<0.01), whereas non-painful esophageal distension (mean volume=4±2 ml) showed a decrease (at 30 minutes: 72±8 vs. 88±12 µV, p<0.03). Thenar responses were unaffected. Conclusions: Painful and non-painful stimuli induce different patterns of esophageal cortico-bulbar excitability suggesting a physiological link between cortical plasticity and visceral pain.







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