4.6 Article

Relay of peripheral oxytocin to central oxytocin neurons via vagal afferents for regulating feeding

Journal

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2019.09.039

Keywords

Oxytocin; Vagal afferents; Paraventricular nucleus; Food intake

Funding

  1. Japan Society for the Promotion of Science (JSPS) [26460302]
  2. Pharmacological Research Foundation, Tokyo
  3. JSPS [26670453, 19H04045]
  4. Programs for Strategic Research Foundation at Private Universities 2013-2017 - Ministry of Education, Culture, Sports, Science and Technology of Japan
  5. Advanced Research and Development Programs for Medical Innovation (AMED-CREST) from Japan Agency for Medical Research and Development (AMED)
  6. Strategic Research Program for Brain Science from Japan AMED [18dm0107076h0003]
  7. Grants-in-Aid for Scientific Research [19H04045, 26670453] Funding Source: KAKEN

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Oxytocin (Oxt), a neurohormone synthesized in the neurons of hypothalamic paraventricular nucleus (PVN) and supraoptic nucleus induces milk-ejection and uterine contraction and regulates social behavior, stress responses, memory and food intake. Peripheral (intraperitoneal and subcutaneous) infusion of Oxt decreases food intake and body weight in obese animals via mechanisms involving vagal afferent nerves and in obese subjects when administered nasally. Peripherally injected and intracerebroventricularly injected Oxt inhibit food intake to similar extent and with similar time course. Thus, peripheral Oxt mimics the effects of central Oxt, however, underlying mechanisms are unclear. In the present study we explored whether intraperitoneal Oxt activates Oxt neurons in PVN via vagal afferents and whether this pathway is linked to inhibition of feeding. We here show that intraperitoneal Oxt injection induces c-Fos expression in PVN largely in Oxt neurons and inhibits food intake, and these effects are blunted by subdiaphragmatic vagotomy. The intraperitoneal Oxt-induced inhibition of food intake was blunted in Oxt KO mice, by intracerebroventricular injection of Oxt receptor antagonist, and by vagotomy. These results demonstrate that intraperitoneal Oxt injection activates PVN Oxt neurons via vagal afferent nerves, thereby inhibiting food intake. This vagal afferents-mediated Oxt's peripheral-to-central coupling may serve to promote satiety and possibly a series of neural functions of Oxt and to treat their disorders. (C) 2019 Elsevier Inc. All rights reserved.

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