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1 GI Research, VA Research & Education Foundation, oklahoma city, Oklahoma, United States
2 Division of Gastroenterology, University of Texas Medical Branch at Galveston, Galveston, Texas, United States
3 Internal Medicine, University of Texas Medical Branch, Galveston, Texas, United States; GI Research, VA Research & Education Foundation, oklahoma city, Oklahoma, United States
* To whom correspondence should be addressed. E-mail: jianchen{at}utmb.edu.
The aim of this study was to determine the effects and mechanism of synchronized gastric electrical stimulation (SGES) on gastric contractions and gastric emptying. Methods: The first experiment was designed to study the effects of SGES on antral contractions in 4 randomized sessions. Sessions 1 (control) and 2 (atropine,) were performed in the fasting state, composed of three 30-min periods (baseline, stimulation and recovery). Sessions 3 (control) and 4 (SGES performed during 2nd 20-min period) were performed in the fed state, consisting of two 20-min periods; glucagon was injected after the first 20 min recording. The 2nd experiment was designed to study the effect of SGES on gastric emptying and consisted of two sessions (control and SGES). SGES was delivered with train duration of 0.5-0.8s, and a pulse frequency of 40Hz, width of 2ms and amplitude of 4mA. Results: 1) SGES induced gastric antral contractions in the fasting state. The motility index was 1.3 ± 0.5 at baseline and 6.1 ± 0.7 (P=0.001) during SGES. This excitatory effect was completely blocked by atropine. 2). SGES enhanced postprandial antral contractions impaired by glucagon. 3) SGES significantly accelerated glucagon-induced delayed gastric emptying. Gastric emptying was 25.5 ± 11.3% without SGES and 38.3 ± 10.7% with SGES (P=0.006 vs. control). Conclusions: This novel method of SGES induces gastric antral contractions in the fasting state, enhances glucagon-induced antral hypomotility in the fed state and accelerates glucagon-induced delayed gastric emptying. The effect of synchronized GES on antral contractions is mediated via the cholinergic pathway.
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