Gating of social reward by oxytocin in the ventral tegmental area

The reward generated by social interactions is critical for promoting prosocial behaviors. Here we present evidence that oxytocin (OXT) release in the ventral tegmental area (VTA), a key node of the brain's reward circuitry, is necessary to elicit social reward. During social interactions, acti...

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Veröffentlicht in:Science (American Association for the Advancement of Science) Jg. 357; H. 6358; S. 1406
Hauptverfasser: Hung, Lin W, Neuner, Sophie, Polepalli, Jai S, Beier, Kevin T, Wright, Matthew, Walsh, Jessica J, Lewis, Eastman M, Luo, Liqun, Deisseroth, Karl, Dölen, Gül, Malenka, Robert C
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Sprache:Englisch
Veröffentlicht: United States 29.09.2017
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ISSN:1095-9203, 1095-9203
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Abstract The reward generated by social interactions is critical for promoting prosocial behaviors. Here we present evidence that oxytocin (OXT) release in the ventral tegmental area (VTA), a key node of the brain's reward circuitry, is necessary to elicit social reward. During social interactions, activity in paraventricular nucleus (PVN) OXT neurons increased. Direct activation of these neurons in the PVN or their terminals in the VTA enhanced prosocial behaviors. Conversely, inhibition of PVN OXT axon terminals in the VTA decreased social interactions. OXT increased excitatory drive onto reward-specific VTA dopamine (DA) neurons. These results demonstrate that OXT promotes prosocial behavior through direct effects on VTA DA neurons, thus providing mechanistic insight into how social interactions can generate rewarding experiences.
AbstractList The reward generated by social interactions is critical for promoting prosocial behaviors. Here we present evidence that oxytocin (OXT) release in the ventral tegmental area (VTA), a key node of the brain's reward circuitry, is necessary to elicit social reward. During social interactions, activity in paraventricular nucleus (PVN) OXT neurons increased. Direct activation of these neurons in the PVN or their terminals in the VTA enhanced prosocial behaviors. Conversely, inhibition of PVN OXT axon terminals in the VTA decreased social interactions. OXT increased excitatory drive onto reward-specific VTA dopamine (DA) neurons. These results demonstrate that OXT promotes prosocial behavior through direct effects on VTA DA neurons, thus providing mechanistic insight into how social interactions can generate rewarding experiences.
The reward generated by social interactions is critical for promoting prosocial behaviors. Here we present evidence that oxytocin (OXT) release in the ventral tegmental area (VTA), a key node of the brain's reward circuitry, is necessary to elicit social reward. During social interactions, activity in paraventricular nucleus (PVN) OXT neurons increased. Direct activation of these neurons in the PVN or their terminals in the VTA enhanced prosocial behaviors. Conversely, inhibition of PVN OXT axon terminals in the VTA decreased social interactions. OXT increased excitatory drive onto reward-specific VTA dopamine (DA) neurons. These results demonstrate that OXT promotes prosocial behavior through direct effects on VTA DA neurons, thus providing mechanistic insight into how social interactions can generate rewarding experiences.The reward generated by social interactions is critical for promoting prosocial behaviors. Here we present evidence that oxytocin (OXT) release in the ventral tegmental area (VTA), a key node of the brain's reward circuitry, is necessary to elicit social reward. During social interactions, activity in paraventricular nucleus (PVN) OXT neurons increased. Direct activation of these neurons in the PVN or their terminals in the VTA enhanced prosocial behaviors. Conversely, inhibition of PVN OXT axon terminals in the VTA decreased social interactions. OXT increased excitatory drive onto reward-specific VTA dopamine (DA) neurons. These results demonstrate that OXT promotes prosocial behavior through direct effects on VTA DA neurons, thus providing mechanistic insight into how social interactions can generate rewarding experiences.
Author Lewis, Eastman M
Walsh, Jessica J
Malenka, Robert C
Deisseroth, Karl
Luo, Liqun
Dölen, Gül
Neuner, Sophie
Beier, Kevin T
Wright, Matthew
Hung, Lin W
Polepalli, Jai S
Author_xml – sequence: 1
  givenname: Lin W
  orcidid: 0000-0003-1184-1035
  surname: Hung
  fullname: Hung, Lin W
  organization: The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia
– sequence: 2
  givenname: Sophie
  orcidid: 0000-0002-3465-9706
  surname: Neuner
  fullname: Neuner, Sophie
  organization: Nancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA
– sequence: 3
  givenname: Jai S
  orcidid: 0000-0003-2004-2163
  surname: Polepalli
  fullname: Polepalli, Jai S
  organization: Nancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA
– sequence: 4
  givenname: Kevin T
  surname: Beier
  fullname: Beier, Kevin T
  organization: Department of Biology, Stanford University, Stanford, CA, USA
– sequence: 5
  givenname: Matthew
  orcidid: 0000-0001-7131-7492
  surname: Wright
  fullname: Wright, Matthew
  organization: Departments of Bioengineering and Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA
– sequence: 6
  givenname: Jessica J
  surname: Walsh
  fullname: Walsh, Jessica J
  organization: Nancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA
– sequence: 7
  givenname: Eastman M
  orcidid: 0000-0003-0647-0719
  surname: Lewis
  fullname: Lewis, Eastman M
  organization: Department of Neuroscience, Johns Hopkins University, Baltimore, MD, USA
– sequence: 8
  givenname: Liqun
  orcidid: 0000-0001-5467-9264
  surname: Luo
  fullname: Luo, Liqun
  organization: Department of Biology, Stanford University, Stanford, CA, USA
– sequence: 9
  givenname: Karl
  orcidid: 0000-0001-9440-3967
  surname: Deisseroth
  fullname: Deisseroth, Karl
  organization: Departments of Bioengineering and Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA
– sequence: 10
  givenname: Gül
  orcidid: 0000-0003-1780-995X
  surname: Dölen
  fullname: Dölen, Gül
  organization: Department of Neuroscience, Johns Hopkins University, Baltimore, MD, USA
– sequence: 11
  givenname: Robert C
  orcidid: 0000-0002-5428-5211
  surname: Malenka
  fullname: Malenka, Robert C
  email: malenka@stanford.edu
  organization: Nancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA. malenka@stanford.edu
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28963257$$D View this record in MEDLINE/PubMed
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Snippet The reward generated by social interactions is critical for promoting prosocial behaviors. Here we present evidence that oxytocin (OXT) release in the ventral...
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SubjectTerms Animals
Dopaminergic Neurons - physiology
Integrases
Interpersonal Relations
Mice
Mice, Knockout
Oxytocin - genetics
Oxytocin - secretion
Paraventricular Hypothalamic Nucleus - cytology
Presynaptic Terminals - physiology
Reward
Social Behavior
Ventral Tegmental Area - secretion
Title Gating of social reward by oxytocin in the ventral tegmental area
URI https://www.ncbi.nlm.nih.gov/pubmed/28963257
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