4.7 Article

Oxytocin Exerts Antidepressant-like effect by potentiating dopaminergic synaptic transmission in the mPFC

Journal

NEUROPHARMACOLOGY
Volume 162, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuropharm.2019.107836

Keywords

Oxytocin; mPFC; Dopamine; Antidepressant effect

Funding

  1. National Natural Science Foundation of China [81771188, 31671049, 81901376]
  2. Ministry of Science and Technology of the People's Republic of China [2013CB91060101]
  3. China Postdoctoral Science Foundation [2017M621535]
  4. Fundamental Research Funds for the Central Universities [22120180534]
  5. Shanghai Municipal Commission of Health and Family Planning [201740072]
  6. Science and Technology Commission of Shanghai Municipality [14411966700, 16411967400]
  7. Pudong New Area Municipal Commission of Health and Family Planning [PW2016D-10]
  8. Personalized Medicines Molecular Signature -based Drug Discovery and Development, Strategic Priority Research Program of the Chinese Academy of Sciences [XDA12040302, XDA12040214]

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Oxytocin (OT) and dopamine (DA) are two important elements that are closely related to mental and reward processes in the brain. OT controlled DA functional regulation contributes to various behaviours such as social reward, social cognition and emotion-related behaviours. Previous studies indicated that diminished dopaminergic transmission in the medial prefrontal cortex (mPFC) is correlated with the pathophysiology of depression. However, the interaction of OT and DA and their roles in antidepressant effects still require further exploration. Here, we investigated the antidepressant effect of OT through local mPFC administration, and further explored the underlying mechanisms that indicated that OT could strengthen dopaminergic synaptic transmission with OT receptor (OTR) activation dependent in the mPFC. Our results showed that local administration of OT in the mPFC exerts antidepressant (-like) effects in both naive and social defeat stress (SDS) depressive animal model. Mechanism study suggested that OT enhances DA level with OTR activation dependent, and elevated mPFC DA levels might further enhance excitatory synaptic transmission by activating the D1/PKA/DARPP32 intracellular signalling pathway in the mPFC. Hence, our study revealed that the activation of OTR strengthens excitatory synaptic transmission via the potentiation of dopaminergic synaptic transmission, especially via D1R activation dependent, in the mPFC, which may be the underlying mechanism of antidepressant (-like) effects mediated by OT. With specifically activation of the D1/PKA/DAPRR32 signalling pathway, our results may augment the important role of OT in reward circuits in the central nervous system.

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