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Vagal oxytocin receptors are necessary for esophageal motility and function
Mohammed Asker, Jean-Philippe Krieger, Ivana Maric, Emre Bedel, Jenny Steen, Stina Börchers, Yuxiang Wen, Francesco Longo, Patrik Aronsson, Michael Winder, Robert P. Doyle, Matthew R. Hayes, Karolina P. Skibicka
Mohammed Asker, Jean-Philippe Krieger, Ivana Maric, Emre Bedel, Jenny Steen, Stina Börchers, Yuxiang Wen, Francesco Longo, Patrik Aronsson, Michael Winder, Robert P. Doyle, Matthew R. Hayes, Karolina P. Skibicka
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Research Article Gastroenterology Neuroscience

Vagal oxytocin receptors are necessary for esophageal motility and function

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Abstract

Oxytocin plays a key role in reproductive physiology but has recently garnered interest for its involvement in modulating feeding behavior. The vagus nerve contributes to feeding behavior control, as well as other gastrointestinal functions. Oxytocin receptors (OTR) are expressed on the vagus, but their role is poorly understood. Herein, we evaluated the contribution of the vagal OTR to food intake and body weight control in male and female rats. Virogenetic knockdown of vagal OTR resulted in reduced body weight and food intake in male rats. Loss of OTR in the vagus also resulted in suppressed locomotor activity in males but hyperactivity in females. Importantly, rats with vagal OTR knockdown, but not controls, exhibited a significantly elevated mortality rate starting 4 weeks after knockdown, with males being disproportionately affected. Mortality followed large eating bouts and was accompanied by abnormal presence of food in the mouth and esophagus, suggesting death by aspiration or food in the airways and suggesting a crucial role of vagal OTR in upper gastrointestinal tract motility. Furthermore, in vivo experiments revealed impaired esophageal transit. Ex vivo findings indicated oxytocin’s contribution to lower esophageal sphincter contraction. Our findings demonstrated a critical role for the oxytocin system: essential function of vagal OTR for esophageal transit and swallowing.

Authors

Mohammed Asker, Jean-Philippe Krieger, Ivana Maric, Emre Bedel, Jenny Steen, Stina Börchers, Yuxiang Wen, Francesco Longo, Patrik Aronsson, Michael Winder, Robert P. Doyle, Matthew R. Hayes, Karolina P. Skibicka

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Figure 2

OTR knockdown affects home-cage locomotor activity in a sex-divergent manner, with no concomitant changes in core body temperature.

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OTR knockdown affects home-cage locomotor activity in a sex-divergent ma...
(A and B) Telemetric home-cage recording of home-cage locomotor activity over 50 days, with cumulative activity during light and dark cycle phases shown in males and females. (C–I) Cumulative home-cage locomotor activity decreases in males (C) and increases in females (D) after nodose OTR knockdown. Analysis of cumulative activity at 7 weeks (E) confirms these sex differences. No difference in activity was detected during the light phase in males; however, a clear trend for a reduced activity is present (F). Females show an increased locomotion after OTR Kd (G). Similar changes are identified for dark phase locomotor activity, with reductions detected in males (H) and increases in activity found in females (I) with OTR knockdown. (J–O) Core body temperature recordings over 50 days indicate no effect of OTR Kd on this parameter in either sex. However, as expected all females, irrespective of treatment, display higher average body temperatures than males during all phases, analyzed over first 3 weeks (L), or latter 4 weeks (M) after OTR Kd. Similar differences are also seen segregating temperature data by light (N) and dark (O) phases. Data are shown as mean ± SEM and analyzed by 2-way ANOVA and post hoc Holm-Šidák; n = 3–5 for males and n = 5 for females. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001.

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