It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Animal brains have evolved to encode social stimuli and transform these representations into advantageous behavioral responses. The commonalities and differences of these representations across species are not well-understood. Here, we show that social isolation activates an oxytocinergic (OXT), nociceptive circuit in the larval zebrafish hypothalamus and that chemical cues released from conspecific animals are potent modulators of this circuit’s activity. We delineate an olfactory to subpallial pathway that transmits chemical social cues to OXT circuitry, where they are transformed into diverse outputs simultaneously regulating avoidance and feeding behaviors. Our data allow us to propose a model through which social stimuli are integrated within a fundamental neural circuit to mediate diverse adaptive behaviours.
Social interactions are known to guide behaviour, but how different species represent social stimuli is poorly understood. In this study, the authors demonstrate how social cues in the larval zebrafish suppress an oxytocinergic circuit, which regulates avoidance and feeding behaviour.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details




1 Harvard University, Department of Molecular and Cellular Biology and Center for Brain Science, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Program in Neuroscience, Department of Neurobiology, Harvard Medical School, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Institute of Molecular and Cell Biology, A*STAR, Singapore (GRID:grid.418812.6) (ISNI:0000 0004 0620 9243)
2 Harvard University, Department of Molecular and Cellular Biology and Center for Brain Science, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X)
3 Harvard University, Department of Molecular and Cellular Biology and Center for Brain Science, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Duke University, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961)