An intrinsic vasopressin system in the olfactory bulb is involved in social recognition

Many peptides, when released as chemical messengers within the brain, have powerful influences on complex behaviours. Most strikingly, vasopressin and oxytocin, once thought of as circulating hormones whose actions were confined to peripheral organs, are now known to be released in the brain, where...

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Published inNature (London) Vol. 464; no. 7287; pp. 413 - 417
Main Authors Ludwig, Mike, Langnaese, Kristina, Tobin, Vicky A, Wacker, Douglas W, Meddle, Simone L, Takayanagi, Yuki, Onaka, Tatsushi, Leng, Gareth, Landgraf, Rainer, Caquineau, Celine, Engelmann, Mario, Hashimoto, Hirofumi, Noack, Julia
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 18.03.2010
Nature Publishing Group
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Summary:Many peptides, when released as chemical messengers within the brain, have powerful influences on complex behaviours. Most strikingly, vasopressin and oxytocin, once thought of as circulating hormones whose actions were confined to peripheral organs, are now known to be released in the brain, where they have fundamentally important roles in social behaviours. In humans, disruptions of these peptide systems have been linked to several neurobehavioural disorders, including Prader-Willi syndrome, affective disorders and obsessive-compulsive disorder, and polymorphisms of V1a vasopressin receptor have been linked to autism. Here we report that the rat olfactory bulb contains a large population of interneurons which express vasopressin, that blocking the actions of vasopressin in the olfactory bulb impairs the social recognition abilities of rats and that vasopressin agonists and antagonists can modulate the processing of information by olfactory bulb neurons. The findings indicate that social information is processed in part by a vasopressin system intrinsic to the olfactory system.
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Author Contributions: VAT and HH contributed equally. ML, GL, and ME designed the experiments. VAT performed the immunohistochemistry and in vitro electrophysiology as shown in Fig. 1. DWW, SLM and CC performed tracer injections (Fig.1m-o). ME and JN performed receptor antagonist and siRNA study with behavioural analysis as shown in Figs 2b,c and 3 as well as suppl. Figs 1, 2a,b. YT and TO produced TG diphtheria toxin rats and performed behaviour experiments shown in Figs 2d,3c and suppl. Fig 2d-i. KL performed in situ hybridisation and RL the vasopressin radioimmunoassay. HH performed in vivo electrophysiology shown in Fig.4 and suppl. Fig 3. ML, ME, TO, GL and HH performed general data processing and statistical analyses. ML and GL wrote the paper.
ISSN:0028-0836
1476-4687
DOI:10.1038/nature08826