Literature DB >> 26392129

Oxytocin Pathway Genes: Evolutionary Ancient System Impacting on Human Affiliation, Sociality, and Psychopathology.

Ruth Feldman1, Mikhail Monakhov2, Maayan Pratt3, Richard P Ebstein2.   

Abstract

Oxytocin (OT), a nonapeptide signaling molecule originating from an ancestral peptide, appears in different variants across all vertebrate and several invertebrate species. Throughout animal evolution, neuropeptidergic signaling has been adapted by organisms for regulating response to rapidly changing environments. The family of OT-like molecules affects both peripheral tissues implicated in reproduction, homeostasis, and energy balance, as well as neuromodulation of social behavior, stress regulation, and associative learning in species ranging from nematodes to humans. After describing the OT-signaling pathway, we review research on the three genes most extensively studied in humans: the OT receptor (OXTR), the structural gene for OT (OXT/neurophysin-I), and CD38. Consistent with the notion that sociality should be studied from the perspective of social life at the species level, we address human social functions in relation to OT-pathway genes, including parenting, empathy, and using social relationships to manage stress. We then describe associations between OT-pathway genes with psychopathologies involving social dysfunctions such as autism, depression, or schizophrenia. Human research particularly underscored the involvement of two OXTR single nucleotide polymorphisms (rs53576, rs2254298) with fewer studies focusing on other OXTR (rs7632287, rs1042778, rs2268494, rs2268490), OXT (rs2740210, rs4813627, rs4813625), and CD38 (rs3796863, rs6449197) single nucleotide polymorphisms. Overall, studies provide evidence for the involvement of OT-pathway genes in human social functions but also suggest that factors such as gender, culture, and early environment often confound attempts to replicate first findings. We conclude by discussing epigenetics, conceptual implications within an evolutionary perspective, and future directions, especially the need to refine phenotypes, carefully characterize early environments, and integrate observations of social behavior across ecological contexts.
Copyright © 2016 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CD38; Epigenetics; Genetics; OXT; OXTR; Oxytocin

Mesh:

Substances:

Year:  2015        PMID: 26392129     DOI: 10.1016/j.biopsych.2015.08.008

Source DB:  PubMed          Journal:  Biol Psychiatry        ISSN: 0006-3223            Impact factor:   13.382


  101 in total

1.  Epigenetic dysregulation of Oxtr in Tet1-deficient mice has implications for neuropsychiatric disorders.

Authors:  Aaron J Towers; Martine W Tremblay; Leeyup Chung; Xin-Lei Li; Alexandra L Bey; Wenhao Zhang; Xinyu Cao; Xiaoming Wang; Ping Wang; Lara J Duffney; Stephen K Siecinski; Sonia Xu; Yuna Kim; Xiangyin Kong; Simon Gregory; Wei Xie; Yong-Hui Jiang
Journal:  JCI Insight       Date:  2018-12-06

2.  Evidence for Association Between OXTR Gene and ASD Clinical Phenotypes.

Authors:  Lucas de Oliveira Pereira Ribeiro; Pedro Vargas-Pinilla; Djenifer B Kappel; Danae Longo; Josiane Ranzan; Michele Michelin Becker; Rudimar Dos Santos Riesgo; Lavinia Schuler-Faccini; Tatiana Roman; Jaqueline Bohrer Schuch
Journal:  J Mol Neurosci       Date:  2018-06-01       Impact factor: 3.444

3.  Oxytocin- and arginine vasopressin-containing fibers in the cortex of humans, chimpanzees, and rhesus macaques.

Authors:  Christina N Rogers; Amy P Ross; Shweta P Sahu; Ethan R Siegel; Jeromy M Dooyema; Mary Ann Cree; Edward G Stopa; Larry J Young; James K Rilling; H Elliott Albers; Todd M Preuss
Journal:  Am J Primatol       Date:  2018-05-24       Impact factor: 2.371

4.  Adolescents growing up amidst intractable conflict attenuate brain response to pain of outgroup.

Authors:  Jonathan Levy; Abraham Goldstein; Moran Influs; Shafiq Masalha; Orna Zagoory-Sharon; Ruth Feldman
Journal:  Proc Natl Acad Sci U S A       Date:  2016-11-14       Impact factor: 11.205

5.  Transactions Between Substance Use Intervention, the Oxytocin Receptor (OXTR) Gene, and Peer Substance Use Predicting Youth Alcohol Use.

Authors:  H Harrington Cleveland; Amanda M Griffin; Pedro S A Wolf; Richard P Wiebe; Gabriel L Schlomer; Mark E Feinberg; Mark T Greenberg; Richard L Spoth; Cleve Redmond; David J Vandenbergh
Journal:  Prev Sci       Date:  2018-01

6.  Relations between early maternal sensitivity and toddler self-regulation: Exploring variation by oxytocin and dopamine D2 receptor genes.

Authors:  Mairin E Augustine; Esther M Leerkes; Andrew Smolen; Susan D Calkins
Journal:  Dev Psychobiol       Date:  2018-06-13       Impact factor: 3.038

Review 7.  Thalamic integration of social stimuli regulating parental behavior and the oxytocin system.

Authors:  Arpad Dobolyi; Melinda Cservenák; Larry J Young
Journal:  Front Neuroendocrinol       Date:  2018-05-26       Impact factor: 8.606

Review 8.  Oxytocin and vasopressin neural networks: Implications for social behavioral diversity and translational neuroscience.

Authors:  Zachary V Johnson; Larry J Young
Journal:  Neurosci Biobehav Rev       Date:  2017-05       Impact factor: 8.989

9.  Chronic Postnatal Stress Induces Depressive-like Behavior in Male Mice and Programs second-Hit Stress-Induced Gene Expression Patterns of OxtR and AvpR1a in Adulthood.

Authors:  Alexandra Lesse; Kathy Rether; Nicole Gröger; Katharina Braun; Jörg Bock
Journal:  Mol Neurobiol       Date:  2016-08-15       Impact factor: 5.590

10.  Intranasal oxytocin reduces weight gain in diet-induced obese prairie voles.

Authors:  Adele M Seelke; Maya A Rhine; Konterri Khun; Amira N Shweyk; Alexandria M Scott; Jessica M Bond; James L Graham; Peter J Havel; Tami Wolden-Hanson; Karen L Bales; James E Blevins
Journal:  Physiol Behav       Date:  2018-08-23
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