Oxytocin and vasopressin: Signalling, behavioural modulation and potential therapeutic effects
Oxytocin (OT) and vasopressin (AVP) are endogenous ligands for OT and AVP receptors in the brain and in the peripheral system. Several studies demonstrate that OT and AVP have opposite roles in modulating stress, anxiety and social behaviours. Interestingly, both peptides and their receptors exhibit...
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Published in: | British journal of pharmacology Vol. 179; no. 8; pp. 1544 - 1564 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
Blackwell Publishing Ltd
01-04-2022
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Subjects: | |
Online Access: | Get full text |
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Summary: | Oxytocin (OT) and vasopressin (AVP) are endogenous ligands for OT and AVP receptors in the brain and in the peripheral system. Several studies demonstrate that OT and AVP have opposite roles in modulating stress, anxiety and social behaviours. Interestingly, both peptides and their receptors exhibit high sequence homology which could account for the biased signalling interaction of the peptides with OT and AVP receptors. However, how and under which conditions this crosstalk occurs in vivo remains unclear. In this review we shed light on the complexity of the roles of OT and AVP, by focusing on their signalling and behavioural differences and exploring the crosstalk between the receptor systems. Moreover, we discuss the potential of OT and AVP receptors as therapeutic targets to treat human disorders, such as autism, schizophrenia and drug abuse.
LINKED ARTICLES
This article is part of a themed issue on Building Bridges in Neuropharmacology. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.8/issuetoc |
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Bibliography: | Funding information National Council for Scientific and Technological Development, Grant/Award Numbers: #141698/2016‐0, #470070/2012‐9; Coordination for the Improvement of Higher Education Personnel, Grant/Award Number: PROAP‐Social Demand; São Paulo Research Foundation, Grant/Award Number: #2018/05038‐0; National Institute of Health, Grant/Award Numbers: DA008863, NS026880 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-2 |
ISSN: | 0007-1188 1476-5381 |
DOI: | 10.1111/bph.15481 |