Modulating the Oxytocin System During the Perinatal Period: A New Strategy for Neuroprotection of the Immature Brain?

Oxytocin is a neurohypophysal hormone known for its activity during labor and its role in lactation. However, the function of oxytocin (OTX) goes far beyond the peripheral regulation of reproduction, and the central effects of OTX have been extensively investigated, since it has been recognized to i...

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Published inFrontiers in neurology Vol. 9; p. 229
Main Authors Zinni, Manuela, Colella, Marina, Batista Novais, Aline Rideau, Baud, Olivier, Mairesse, Jérôme
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media 13.04.2018
Frontiers Media S.A
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Summary:Oxytocin is a neurohypophysal hormone known for its activity during labor and its role in lactation. However, the function of oxytocin (OTX) goes far beyond the peripheral regulation of reproduction, and the central effects of OTX have been extensively investigated, since it has been recognized to influence the learning and memory processes. OTX has also prominent effects on social behavior, anxiety, and autism. Interaction between glucocorticoids, OTX, and maternal behavior may have long-term effects on the developmental program of the developing brain subjected to adverse events during pre and perinatal periods. OTX treatment in humans improves many aspects of social cognition and behavior. Its effects on the hypothalamic-pituitary-adrenal axis and inflammation appear to be of interest in neonates because these properties may confer benefits when the perinatal brain has been subjected to injury. Indeed, early life inflammation and abnormal adrenal response to stress have been associated with an abnormal white matter development. Recent investigations demonstrated that OTX is involved in the modulation of microglial reactivity in the developing brain. This review recapitulates state-of-the art data supporting the hypothesis that the OTX system could be considered as an innovative candidate for neuroprotection, especially in the immature brain.
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PMCID: PMC5908892
Edited by: Carl E. Stafstrom, Johns Hopkins Medicine, United States
Specialty section: This article was submitted to Pediatric Neurology, a section of the journal Frontiers in Neurology
These authors have contributed equally to this work.
Reviewed by: Yehezkel Ben-Ari, Neurochlore, France; Akira Monji, Saga University, Japan
ISSN:1664-2295
1664-2295
DOI:10.3389/fneur.2018.00229