Effects of general anesthesia on myoelectric activity of the intestine in horses

G. D. Lester From the Department of Applied Veterinary Medicine, School of Veterinary Studies (Lester, Bolton, Cullen), and the School of Mathematical and Physical Sciences (Thurgate), Murdoch University, Western Australia 6150.

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J. R. Bolton From the Department of Applied Veterinary Medicine, School of Veterinary Studies (Lester, Bolton, Cullen), and the School of Mathematical and Physical Sciences (Thurgate), Murdoch University, Western Australia 6150.

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L. K. Cullen From the Department of Applied Veterinary Medicine, School of Veterinary Studies (Lester, Bolton, Cullen), and the School of Mathematical and Physical Sciences (Thurgate), Murdoch University, Western Australia 6150.

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S. M. Thurgate From the Department of Applied Veterinary Medicine, School of Veterinary Studies (Lester, Bolton, Cullen), and the School of Mathematical and Physical Sciences (Thurgate), Murdoch University, Western Australia 6150.

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SUMMARY

Myoelectric activity was monitored from the terminal ileum, cecum, and colonic pelvic flexure by use of Ag-pAgCl bipolar electrodes in 4 adult horses before, during, and after general anesthesia. Horses were anesthetized by way of 3 commonly used regimens, including xylazine (1.1 mg/kg of body weight) and ketamine hydrochloride (2.2 mg/kg); thiopental sodium (7.7 mg/kg), followed by halothane vaporized in oxygen; and thiopental sodium (2.5 g) in guaifenesin (100 mg/ml) solution given to effect, followed by halothane in oxygen. All 3 anesthetic regimens decreased intestinal spike-burst activity in the areas monitored. The slowest return to preanesthetic myoelectric activity was observed after xylazine and ketamine administration. After both of the barbiturate/halothane anesthetic regimens, there was a rebound increase in spike-burst frequency, without alteration in the proportion of propagative myoelectric events. All 3 anesthetic regimens appeared to reset the timing of the small and large intestinal migrating myoelectric complexes. By 9 hours after recovery from anesthesia, the effects of anesthesia, irrespective of regimen, had disappeared. Although anesthesia significantly (P < 0.05) altered intestinal myoelectric activity, no particular anesthetic regimen had a prolonged effect. Results of our study indicate that the particular chosen regimen of general anesthesia is unimportant in development of motility disturbances in horses after anesthesia.

SUMMARY

Myoelectric activity was monitored from the terminal ileum, cecum, and colonic pelvic flexure by use of Ag-pAgCl bipolar electrodes in 4 adult horses before, during, and after general anesthesia. Horses were anesthetized by way of 3 commonly used regimens, including xylazine (1.1 mg/kg of body weight) and ketamine hydrochloride (2.2 mg/kg); thiopental sodium (7.7 mg/kg), followed by halothane vaporized in oxygen; and thiopental sodium (2.5 g) in guaifenesin (100 mg/ml) solution given to effect, followed by halothane in oxygen. All 3 anesthetic regimens decreased intestinal spike-burst activity in the areas monitored. The slowest return to preanesthetic myoelectric activity was observed after xylazine and ketamine administration. After both of the barbiturate/halothane anesthetic regimens, there was a rebound increase in spike-burst frequency, without alteration in the proportion of propagative myoelectric events. All 3 anesthetic regimens appeared to reset the timing of the small and large intestinal migrating myoelectric complexes. By 9 hours after recovery from anesthesia, the effects of anesthesia, irrespective of regimen, had disappeared. Although anesthesia significantly (P < 0.05) altered intestinal myoelectric activity, no particular anesthetic regimen had a prolonged effect. Results of our study indicate that the particular chosen regimen of general anesthesia is unimportant in development of motility disturbances in horses after anesthesia.

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