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dc.contributor.author Sharma, Samata R
dc.contributor.author Gonda, Xénia
dc.contributor.author Döme, Péter
dc.contributor.author Tarazi, Frank I
dc.date.accessioned 2020-07-28T12:22:32Z
dc.date.available 2020-07-28T12:22:32Z
dc.date.issued 2020
dc.identifier 85086649717
dc.identifier.citation journalVolume=214;pagination= Paper 107602,15 pages;journalTitle=PHARMACOLOGY & THERAPEUTICS;journalAbbreviatedTitle=PHARMACOL THERAPEUT;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/8405
dc.identifier.uri doi:10.1016/j.pharmthera.2020.107602
dc.description.abstract Oxytocin (OT) is a neurohypophysial hormone and neuropeptide produced by the hypothalamus and released by the pituitary gland. It has multiple physiological roles including stimulation of parturition and lactation, and promotion of pro-adaptive social behaviors necessary for mammalian survival. OT interacts with one receptor subtype: the OT receptor (OTR), which, upon stimulation, triggers different intracellular signal transduction cascades to mediate its physiological actions. Preclinical studies show that OT regulates social behaviors such as pair bonding, recognition and social interaction. It also coordinates the activation of the hypothalamic-pituitary-adrenal (HPA) axis and the release of corticotrophin-releasing hormone. Further evidence suggests that OT plays an important role in regulating caloric intake and metabolism, and in maintaining electrolyte and cardiovascular homeostasis. OT is also involved in attenuating the neurophysiological and neurochemical effects of trauma on the brain and body by facilitating both physical attachment such as wound healing, and psychological/social attachment, thereby increasing resilience to subsequent traumatic events. Clinical trials have reported that intranasal administration of OT provides therapeutic benefits for patients diagnosed with traumatic stress-related diseases such as major depressive disorders and post-traumatic stress disorder. OT's therapeutic benefits may result from context-dependent interactions with key neural pathways (social, cognitive, and reward), neurotransmitters (dopamine, norepinephrine, serotonin, and endogenous opioids), and biomarkers (adrenocorticotropic hormone, cortisol, and dehydroepiandrosterone sulfate), that lead to a decrease in stress associated behaviors, and facilitate post-traumatic growth, ultimately leading to increased resilience, through improved social cohesion and attachment. OT induced-augmentation of physical and cognitive resilience may play a significant role in both the prevention of, and improved clinical outcomes for, traumatic stress-related disorders following either acute or enduring traumatic experiences.
dc.title What's Love Got to do with it: Role of oxytocin in trauma, attachment and resilience..
dc.type Journal Article
dc.date.updated 2020-07-25T15:22:50Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 31383651
dc.identifier.scopus 85086649717
dc.identifier.pubmed 32512017
dc.contributor.department SE/GYTK/GYHATAS/MTA-SE Neuropszichofarmakológiai és Neurokémiai Kutatócsoport
dc.contributor.department SE/GYTK/GYHATAS/NAP-A-SE Új Antidepresszív Gyógyszercélpont Kutatócsoport
dc.contributor.department SE/AOK/K/Pszichiátriai és Pszichoterápiás Klinika
dc.contributor.department SE/GYTK/GYHATAS/NAP-2-SE Új Antidepresszív Gyógyszercélpont Kutatócsoport
dc.contributor.institution Semmelweis Egyetem


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