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Evidence that oxytocin exerts anxiolytic effects via oxytocin receptor expressed in serotonergic neurons in mice.

http://www.ncbi.nlm.nih.gov/pubmed/19228979

The oxytocin receptor has been implicated in the regulation of reproductive physiology as well as social and emotional behaviors. The neurochemical mechanisms by which oxytocin receptor modulates social and emotional behavior remains elusive, in part because of a lack of sensitive and selective antibodies for cellular localization. To more precisely characterize oxytocin receptor-expressing neurons within the brain, we generated an oxytocin receptor-reporter mouse in which part of the oxytocin receptor gene was replaced with Venus cDNA (a variant of yellow fluorescent protein). Examination of the Venus expression revealed that, in the raphe nuclei, about one-half of tryptophan hydroxylase-immunoreactive neurons were positive for Venus, suggesting a potential role for oxytocin in the modulation of serotonin release. Oxytocin infusion facilitated serotonin release within the median raphe nucleus and reduced anxiety-related behavior. Infusion of a 5-HT(2A/2C) receptor antagonist blocked the anxiolytic effect of oxytocin, suggesting that oxytocin receptor activation in serotonergic neurons mediates the anxiolytic effects of oxytocin. This is the first demonstration that oxytocin may regulate serotonin release and exert anxiolytic effects via direct activation of oxytocin receptor expressed in serotonergic neurons of the raphe nuclei. These results also have important implications for psychiatric disorders such as autism and depression in which both the oxytocin and serotonin systems have been implicated.

Pubmed ID: 19228979 RIS Download

Mesh terms: Animals | Anti-Anxiety Agents | Anxiety Disorders | Bacterial Proteins | Brain | Chimera | Female | Gene Knock-In Techniques | Luminescent Proteins | Male | Mice | Mice, Inbred C57BL | Mice, Transgenic | Oxytocin | Raphe Nuclei | Receptor, Serotonin, 5-HT2A | Receptors, Oxytocin | Serotonin | Serotonin 5-HT2 Receptor Antagonists | Synaptic Transmission | Tryptophan Hydroxylase

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Associated grants

  • Agency: NIMH NIH HHS, Id: MH64692

Comparative Toxicogenomics Database (Data, Disease Annotation)

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