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Published in: Neuroscience Bulletin 2/2017

Open Access 01-04-2017 | Review

Genes Related to Oxytocin and Arginine-Vasopressin Pathways: Associations with Autism Spectrum Disorders

Authors: Rong Zhang, Hong-Feng Zhang, Ji-Sheng Han, Song-Ping Han

Published in: Neuroscience Bulletin | Issue 2/2017

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Abstract

Autism spectrum disorder (ASD) is a highly heritable neurodevelopmental disorders characterized by impaired social interactions, communication deficits, and repetitive behavior. Although the mechanisms underlying its etiology and manifestations are poorly understood, several lines of evidence from rodent and human studies suggest involvement of the evolutionarily highly-conserved oxytocin (OXT) and arginine-vasopressin (AVP), as these neuropeptides modulate various aspects of mammalian social behavior. As far as we know, there is no comprehensive review of the roles of the OXT and AVP systems in the development of ASD from the genetic aspect. In this review, we summarize the current knowledge regarding associations between ASD and single-nucleotide variants of the human OXT-AVP pathway genes OXT, AVP, AVP receptor 1a (AVPR1a), OXT receptor (OXTR), the oxytocinase/vasopressinase (LNPEP), and ADP-ribosyl cyclase (CD38).
Literature
1.
go back to reference Zablotsky B, Black LI, Maenner MJ, Schieve LA, Blumberg SJ. Estimated prevalence of autism and other developmental disabilities following questionnaire changes in the 2014 national health interview survey. Natl Health Stat Report 2015: 1–20. Zablotsky B, Black LI, Maenner MJ, Schieve LA, Blumberg SJ. Estimated prevalence of autism and other developmental disabilities following questionnaire changes in the 2014 national health interview survey. Natl Health Stat Report 2015: 1–20.
2.
go back to reference Hens K, Peeters H, Dierickx K. The ethics of complexity. Genetics and autism, a literature review. Am J Med Genet B Neuropsychiatr Genet 2016, 171B: 305–316.PubMedCrossRef Hens K, Peeters H, Dierickx K. The ethics of complexity. Genetics and autism, a literature review. Am J Med Genet B Neuropsychiatr Genet 2016, 171B: 305–316.PubMedCrossRef
3.
go back to reference Ronemus M, Iossifov I, Levy D, Wigler M. The role of de novo mutations in the genetics of autism spectrum disorders. Nat Rev Genet 2014, 15: 133–141.PubMedCrossRef Ronemus M, Iossifov I, Levy D, Wigler M. The role of de novo mutations in the genetics of autism spectrum disorders. Nat Rev Genet 2014, 15: 133–141.PubMedCrossRef
4.
go back to reference Tchaconas A, Adesman A. Autism spectrum disorders: a pediatric overview and update. Curr Opin Pediatr 2013, 25: 130–144.PubMedCrossRef Tchaconas A, Adesman A. Autism spectrum disorders: a pediatric overview and update. Curr Opin Pediatr 2013, 25: 130–144.PubMedCrossRef
5.
go back to reference Szatmari P. Is autism, at least in part, a disorder of fetal programming? Arch Gen Psychiatry 2011, 68: 1091–1092.PubMedCrossRef Szatmari P. Is autism, at least in part, a disorder of fetal programming? Arch Gen Psychiatry 2011, 68: 1091–1092.PubMedCrossRef
6.
go back to reference Constantino JN, Zhang Y, Frazier T, Abbacchi AM, Law P. Sibling recurrence and the genetic epidemiology of autism. Am J Psychiatry 2010, 167: 1349–1356.PubMedPubMedCentralCrossRef Constantino JN, Zhang Y, Frazier T, Abbacchi AM, Law P. Sibling recurrence and the genetic epidemiology of autism. Am J Psychiatry 2010, 167: 1349–1356.PubMedPubMedCentralCrossRef
7.
go back to reference Gratten J, Wray NR, Keller MC, Visscher PM. Large-scale genomics unveils the genetic architecture of psychiatric disorders. Nat Neurosci 2014, 17: 782–790.PubMedPubMedCentralCrossRef Gratten J, Wray NR, Keller MC, Visscher PM. Large-scale genomics unveils the genetic architecture of psychiatric disorders. Nat Neurosci 2014, 17: 782–790.PubMedPubMedCentralCrossRef
8.
go back to reference Donaldson ZR, Young LJ. Oxytocin, vasopressin, and the neurogenetics of sociality. Science 2008, 322: 900–904.PubMedCrossRef Donaldson ZR, Young LJ. Oxytocin, vasopressin, and the neurogenetics of sociality. Science 2008, 322: 900–904.PubMedCrossRef
9.
go back to reference Meyer-Lindenberg A, Domes G, Kirsch P, Heinrichs M. Oxytocin and vasopressin in the human brain: social neuropeptides for translational medicine. Nat Rev Neurosci 2011, 12: 524–538.PubMedCrossRef Meyer-Lindenberg A, Domes G, Kirsch P, Heinrichs M. Oxytocin and vasopressin in the human brain: social neuropeptides for translational medicine. Nat Rev Neurosci 2011, 12: 524–538.PubMedCrossRef
10.
go back to reference Lukas M, Neumann ID. Oxytocin and vasopressin in rodent behaviors related to social dysfunctions in autism spectrum disorders. Behav Brain Res 2013, 251: 85–94.PubMedCrossRef Lukas M, Neumann ID. Oxytocin and vasopressin in rodent behaviors related to social dysfunctions in autism spectrum disorders. Behav Brain Res 2013, 251: 85–94.PubMedCrossRef
11.
go back to reference LoParo D, Waldman ID. The oxytocin receptor gene (OXTR) is associated with autism spectrum disorder: a meta-analysis. Mol Psychiatry 2015, 20: 640–646.PubMedCrossRef LoParo D, Waldman ID. The oxytocin receptor gene (OXTR) is associated with autism spectrum disorder: a meta-analysis. Mol Psychiatry 2015, 20: 640–646.PubMedCrossRef
12.
go back to reference Wassink TH, Piven J, Vieland VJ, Pietila J, Goedken RJ, Folstein SE, et al. Examination of AVPR1a as an autism susceptibility gene. Mol Psychiatry 2004, 9: 968–972.PubMedCrossRef Wassink TH, Piven J, Vieland VJ, Pietila J, Goedken RJ, Folstein SE, et al. Examination of AVPR1a as an autism susceptibility gene. Mol Psychiatry 2004, 9: 968–972.PubMedCrossRef
13.
go back to reference Malavasi F, Deaglio S, Funaro A, Ferrero E, Horenstein AL, Ortolan E, et al. Evolution and function of the ADP ribosyl cyclase/CD38 gene family in physiology and pathology. Physiol Rev 2008, 88: 841–886.PubMedCrossRef Malavasi F, Deaglio S, Funaro A, Ferrero E, Horenstein AL, Ortolan E, et al. Evolution and function of the ADP ribosyl cyclase/CD38 gene family in physiology and pathology. Physiol Rev 2008, 88: 841–886.PubMedCrossRef
14.
go back to reference Jin D, Liu HX, Hirai H, Torashima T, Nagai T, Lopatina O, et al. CD38 is critical for social behaviour by regulating oxytocin secretion. Nature 2007, 446: 41–45.PubMedCrossRef Jin D, Liu HX, Hirai H, Torashima T, Nagai T, Lopatina O, et al. CD38 is critical for social behaviour by regulating oxytocin secretion. Nature 2007, 446: 41–45.PubMedCrossRef
15.
go back to reference Lerer E, Levi S, Israel S, Yaari M, Nemanov L, Mankuta D, et al. Low CD38 expression in lymphoblastoid cells and haplotypes are both associated with autism in a family-based study. Autism Res 2010, 3: 293–302.PubMedCrossRef Lerer E, Levi S, Israel S, Yaari M, Nemanov L, Mankuta D, et al. Low CD38 expression in lymphoblastoid cells and haplotypes are both associated with autism in a family-based study. Autism Res 2010, 3: 293–302.PubMedCrossRef
16.
go back to reference Tsujimoto M, Hattori A. The oxytocinase subfamily of M1 aminopeptidases. Biochim Biophys Acta 2005, 1751: 9–18.PubMedCrossRef Tsujimoto M, Hattori A. The oxytocinase subfamily of M1 aminopeptidases. Biochim Biophys Acta 2005, 1751: 9–18.PubMedCrossRef
17.
go back to reference Rao VV, Loffler C, Battey J, Hansmann I. The human gene for oxytocin-neurophysin I (OXT) is physically mapped to chromosome 20p13 by in situ hybridization. Cytogenet Cell Genet 1992, 61: 271–273.PubMedCrossRef Rao VV, Loffler C, Battey J, Hansmann I. The human gene for oxytocin-neurophysin I (OXT) is physically mapped to chromosome 20p13 by in situ hybridization. Cytogenet Cell Genet 1992, 61: 271–273.PubMedCrossRef
18.
go back to reference Gimpl G, Fahrenholz F. The oxytocin receptor system: structure, function, and regulation. Physiol Rev 2001, 81: 629–683.PubMed Gimpl G, Fahrenholz F. The oxytocin receptor system: structure, function, and regulation. Physiol Rev 2001, 81: 629–683.PubMed
19.
go back to reference Feldman R, Monakhov M, Pratt M, Ebstein RP. Oxytocin pathway genes: evolutionary ancient system impacting on human affiliation, sociality, and psychopathology. Biol Psychiatry 2016, 79: 174–184.PubMedCrossRef Feldman R, Monakhov M, Pratt M, Ebstein RP. Oxytocin pathway genes: evolutionary ancient system impacting on human affiliation, sociality, and psychopathology. Biol Psychiatry 2016, 79: 174–184.PubMedCrossRef
20.
go back to reference Ruppert S, Scherer G, Schutz G. Recent gene conversion involving bovine vasopressin and oxytocin precursor genes suggested by nucleotide sequence. Nature 1984, 308: 554–557.PubMedCrossRef Ruppert S, Scherer G, Schutz G. Recent gene conversion involving bovine vasopressin and oxytocin precursor genes suggested by nucleotide sequence. Nature 1984, 308: 554–557.PubMedCrossRef
21.
go back to reference Allen-Brady K, Miller J, Matsunami N, Stevens J, Block H, Farley M, et al. A high-density SNP genome-wide linkage scan in a large autism extended pedigree. Mol Psychiatry 2009, 14: 590–600.PubMedCrossRef Allen-Brady K, Miller J, Matsunami N, Stevens J, Block H, Farley M, et al. A high-density SNP genome-wide linkage scan in a large autism extended pedigree. Mol Psychiatry 2009, 14: 590–600.PubMedCrossRef
22.
go back to reference Ebstein RP, Israel S, Lerer E, Uzefovsky F, Shalev I, Gritsenko I, et al. Arginine vasopressin and oxytocin modulate human social behavior. Ann N Y Acad Sci 2009, 1167: 87–102.PubMedCrossRef Ebstein RP, Israel S, Lerer E, Uzefovsky F, Shalev I, Gritsenko I, et al. Arginine vasopressin and oxytocin modulate human social behavior. Ann N Y Acad Sci 2009, 1167: 87–102.PubMedCrossRef
23.
go back to reference Hovey D, Zettergren A, Jonsson L, Melke J, Anckarsater H, Lichtenstein P, et al. Associations between oxytocin-related genes and autistic-like traits. Soc Neurosci 2014, 9: 378–386.PubMedCrossRef Hovey D, Zettergren A, Jonsson L, Melke J, Anckarsater H, Lichtenstein P, et al. Associations between oxytocin-related genes and autistic-like traits. Soc Neurosci 2014, 9: 378–386.PubMedCrossRef
24.
go back to reference Yrigollen CM, Han SS, Kochetkova A, Babitz T, Chang JT, Volkmar FR, et al. Genes controlling affiliative behavior as candidate genes for autism. Biol Psychiatry 2008, 63: 911–916.PubMedPubMedCentralCrossRef Yrigollen CM, Han SS, Kochetkova A, Babitz T, Chang JT, Volkmar FR, et al. Genes controlling affiliative behavior as candidate genes for autism. Biol Psychiatry 2008, 63: 911–916.PubMedPubMedCentralCrossRef
25.
go back to reference Francis SM, Kistner-Griffin E, Yan Z, Guter S, Cook EH, Jacob S. Variants in adjacent oxytocin/vasopressin gene region and associations with ASD diagnosis and other autism related endophenotypes. Front Neurosci 2016, 10: 195.PubMedPubMedCentral Francis SM, Kistner-Griffin E, Yan Z, Guter S, Cook EH, Jacob S. Variants in adjacent oxytocin/vasopressin gene region and associations with ASD diagnosis and other autism related endophenotypes. Front Neurosci 2016, 10: 195.PubMedPubMedCentral
27.
go back to reference Jonas W, Mileva-Seitz V, Girard AW, Bisceglia R, Kennedy JL, Sokolowski M, et al. Genetic variation in oxytocin rs2740210 and early adversity associated with postpartum depression and breastfeeding duration. Genes Brain Behav 2013, 12: 681–694.PubMed Jonas W, Mileva-Seitz V, Girard AW, Bisceglia R, Kennedy JL, Sokolowski M, et al. Genetic variation in oxytocin rs2740210 and early adversity associated with postpartum depression and breastfeeding duration. Genes Brain Behav 2013, 12: 681–694.PubMed
28.
go back to reference Mileva-Seitz V, Steiner M, Atkinson L, Meaney MJ, Levitan R, Kennedy JL, et al. Interaction between oxytocin genotypes and early experience predicts quality of mothering and postpartum mood. PLoS One 2013, 8: e61443.PubMedPubMedCentralCrossRef Mileva-Seitz V, Steiner M, Atkinson L, Meaney MJ, Levitan R, Kennedy JL, et al. Interaction between oxytocin genotypes and early experience predicts quality of mothering and postpartum mood. PLoS One 2013, 8: e61443.PubMedPubMedCentralCrossRef
29.
go back to reference Love TM, Enoch MA, Hodgkinson CA, Pecina M, Mickey B, Koeppe RA, et al. Oxytocin gene polymorphisms influence human dopaminergic function in a sex-dependent manner. Biol Psychiatry 2012, 72: 198–206.PubMedPubMedCentralCrossRef Love TM, Enoch MA, Hodgkinson CA, Pecina M, Mickey B, Koeppe RA, et al. Oxytocin gene polymorphisms influence human dopaminergic function in a sex-dependent manner. Biol Psychiatry 2012, 72: 198–206.PubMedPubMedCentralCrossRef
30.
go back to reference Ludwig M, Leng G. Dendritic peptide release and peptide-dependent behaviours. Nat Rev Neurosci 2006, 7: 126–136.PubMedCrossRef Ludwig M, Leng G. Dendritic peptide release and peptide-dependent behaviours. Nat Rev Neurosci 2006, 7: 126–136.PubMedCrossRef
31.
go back to reference Gazis D. Plasma half-lives of vasopressin and oxytocin analogs after iv injection in rats. Proc Soc Exp Biol Med 1978, 158: 663–665.PubMedCrossRef Gazis D. Plasma half-lives of vasopressin and oxytocin analogs after iv injection in rats. Proc Soc Exp Biol Med 1978, 158: 663–665.PubMedCrossRef
32.
go back to reference Matsumoto H, Nagasaka T, Hattori A, Rogi T, Tsuruoka N, Mizutani S, et al. Expression of placental leucine aminopeptidase/oxytocinase in neuronal cells and its action on neuronal peptides. Eur J Biochem 2001, 268: 3259–3266.PubMedCrossRef Matsumoto H, Nagasaka T, Hattori A, Rogi T, Tsuruoka N, Mizutani S, et al. Expression of placental leucine aminopeptidase/oxytocinase in neuronal cells and its action on neuronal peptides. Eur J Biochem 2001, 268: 3259–3266.PubMedCrossRef
33.
go back to reference Nakada TA, Russell JA, Wellman H, Boyd JH, Nakada E, Thain KR, et al. Leucyl/cystinyl aminopeptidase gene variants in septic shock. Chest 2011, 139: 1042–1049.PubMedCrossRef Nakada TA, Russell JA, Wellman H, Boyd JH, Nakada E, Thain KR, et al. Leucyl/cystinyl aminopeptidase gene variants in septic shock. Chest 2011, 139: 1042–1049.PubMedCrossRef
34.
go back to reference Inoue T, Kimura T, Azuma C, Inazawa J, Takemura M, Kikuchi T, et al. Structural organization of the human oxytocin receptor gene. J Biol Chem 1994, 269: 32451–32456.PubMed Inoue T, Kimura T, Azuma C, Inazawa J, Takemura M, Kikuchi T, et al. Structural organization of the human oxytocin receptor gene. J Biol Chem 1994, 269: 32451–32456.PubMed
35.
go back to reference Wu S, Jia M, Ruan Y, Liu J, Guo Y, Shuang M, et al. Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population. Biol Psychiatry 2005, 58: 74–77.PubMedCrossRef Wu S, Jia M, Ruan Y, Liu J, Guo Y, Shuang M, et al. Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population. Biol Psychiatry 2005, 58: 74–77.PubMedCrossRef
36.
go back to reference Nyffeler J, Walitza S, Bobrowski E, Gundelfinger R, Grunblatt E. Association study in siblings and case-controls of serotonin- and oxytocin-related genes with high functioning autism. J Mol Psychiatry 2014, 2: 1.PubMedPubMedCentralCrossRef Nyffeler J, Walitza S, Bobrowski E, Gundelfinger R, Grunblatt E. Association study in siblings and case-controls of serotonin- and oxytocin-related genes with high functioning autism. J Mol Psychiatry 2014, 2: 1.PubMedPubMedCentralCrossRef
37.
go back to reference Jacob S, Brune CW, Carter CS, Leventhal BL, Lord C, Cook EH, Jr. Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism. Neurosci Lett 2007, 417: 6–9.PubMedPubMedCentralCrossRef Jacob S, Brune CW, Carter CS, Leventhal BL, Lord C, Cook EH, Jr. Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism. Neurosci Lett 2007, 417: 6–9.PubMedPubMedCentralCrossRef
38.
go back to reference Lerer E, Levi S, Salomon S, Darvasi A, Yirmiya N, Ebstein RP. Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition. Mol Psychiatry 2008, 13: 980–988.PubMedCrossRef Lerer E, Levi S, Salomon S, Darvasi A, Yirmiya N, Ebstein RP. Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition. Mol Psychiatry 2008, 13: 980–988.PubMedCrossRef
39.
go back to reference Liu X, Kawamura Y, Shimada T, Otowa T, Koishi S, Sugiyama T, et al. Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population. J Hum Genet 2010, 55: 137–141.PubMedCrossRef Liu X, Kawamura Y, Shimada T, Otowa T, Koishi S, Sugiyama T, et al. Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population. J Hum Genet 2010, 55: 137–141.PubMedCrossRef
40.
go back to reference Kranz TM, Kopp M, Waltes R, Sachse M, Duketis E, Jarczok TA, et al. Meta-analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorder. Autism Res 2016, 9: 1036–1045.PubMedCrossRef Kranz TM, Kopp M, Waltes R, Sachse M, Duketis E, Jarczok TA, et al. Meta-analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorder. Autism Res 2016, 9: 1036–1045.PubMedCrossRef
41.
go back to reference Di Napoli A, Warrier V, Baron-Cohen S, Chakrabarti B. Genetic variation in the oxytocin receptor (OXTR) gene is associated with Asperger Syndrome. Mol Autism 2014, 5: 48.PubMedPubMedCentralCrossRef Di Napoli A, Warrier V, Baron-Cohen S, Chakrabarti B. Genetic variation in the oxytocin receptor (OXTR) gene is associated with Asperger Syndrome. Mol Autism 2014, 5: 48.PubMedPubMedCentralCrossRef
42.
go back to reference Ma WJ, Hashii M, Munesue T, Hayashi K, Yagi K, Yamagishi M, et al. Non-synonymous single-nucleotide variations of the human oxytocin receptor gene and autism spectrum disorders: a case-control study in a Japanese population and functional analysis. Mol Autism 2013, 4: 22.PubMedPubMedCentralCrossRef Ma WJ, Hashii M, Munesue T, Hayashi K, Yagi K, Yamagishi M, et al. Non-synonymous single-nucleotide variations of the human oxytocin receptor gene and autism spectrum disorders: a case-control study in a Japanese population and functional analysis. Mol Autism 2013, 4: 22.PubMedPubMedCentralCrossRef
43.
go back to reference Campbell DB, Datta D, Jones ST, Batey Lee E, Sutcliffe JS, Hammock EA, et al. Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder. J Neurodev Disord 2011, 3: 101–112.PubMedPubMedCentralCrossRef Campbell DB, Datta D, Jones ST, Batey Lee E, Sutcliffe JS, Hammock EA, et al. Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder. J Neurodev Disord 2011, 3: 101–112.PubMedPubMedCentralCrossRef
44.
go back to reference Tansey KE, Brookes KJ, Hill MJ, Cochrane LE, Gill M, Skuse D, et al. Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies. Neurosci Lett 2010, 474: 163–167.PubMedCrossRef Tansey KE, Brookes KJ, Hill MJ, Cochrane LE, Gill M, Skuse D, et al. Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies. Neurosci Lett 2010, 474: 163–167.PubMedCrossRef
45.
go back to reference Wermter AK, Kamp-Becker I, Hesse P, Schulte-Korne G, Strauch K, Remschmidt H. Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level. Am J Med Genet B Neuropsychiatr Genet 2010, 153B: 629–639.PubMed Wermter AK, Kamp-Becker I, Hesse P, Schulte-Korne G, Strauch K, Remschmidt H. Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level. Am J Med Genet B Neuropsychiatr Genet 2010, 153B: 629–639.PubMed
46.
go back to reference Liu X, Kawashima M, Miyagawa T, Otowa T, Latt KZ, Thiri M, et al. Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals. Hum Genome Var 2015, 2: 15024.PubMedPubMedCentralCrossRef Liu X, Kawashima M, Miyagawa T, Otowa T, Latt KZ, Thiri M, et al. Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals. Hum Genome Var 2015, 2: 15024.PubMedPubMedCentralCrossRef
47.
go back to reference Gregory SG, Connelly JJ, Towers AJ, Johnson J, Biscocho D, Markunas CA, et al. Genomic and epigenetic evidence for oxytocin receptor deficiency in autism. BMC Med 2009, 7: 62.PubMedPubMedCentralCrossRef Gregory SG, Connelly JJ, Towers AJ, Johnson J, Biscocho D, Markunas CA, et al. Genomic and epigenetic evidence for oxytocin receptor deficiency in autism. BMC Med 2009, 7: 62.PubMedPubMedCentralCrossRef
48.
go back to reference Puglia MH, Lillard TS, Morris JP, Connelly JJ. Epigenetic modification of the oxytocin receptor gene influences the perception of anger and fear in the human brain. Proc Natl Acad Sci U S A 2015, 112: 3308–3313.PubMedPubMedCentralCrossRef Puglia MH, Lillard TS, Morris JP, Connelly JJ. Epigenetic modification of the oxytocin receptor gene influences the perception of anger and fear in the human brain. Proc Natl Acad Sci U S A 2015, 112: 3308–3313.PubMedPubMedCentralCrossRef
49.
go back to reference Walum H, Lichtenstein P, Neiderhiser JM, Reiss D, Ganiban JM, Spotts EL, et al. Variation in the oxytocin receptor gene is associated with pair-bonding and social behavior. Biol Psychiatry 2012, 71: 419–426.PubMedCrossRef Walum H, Lichtenstein P, Neiderhiser JM, Reiss D, Ganiban JM, Spotts EL, et al. Variation in the oxytocin receptor gene is associated with pair-bonding and social behavior. Biol Psychiatry 2012, 71: 419–426.PubMedCrossRef
51.
go back to reference Klahr AM, Klump K, Burt SA. A constructive replication of the association between the oxytocin receptor genotype and parenting. J Fam Psychol 2015, 29: 91–99.PubMedCrossRef Klahr AM, Klump K, Burt SA. A constructive replication of the association between the oxytocin receptor genotype and parenting. J Fam Psychol 2015, 29: 91–99.PubMedCrossRef
52.
go back to reference Skuse DH, Lori A, Cubells JF, Lee I, Conneely KN, Puura K, et al. Common polymorphism in the oxytocin receptor gene (OXTR) is associated with human social recognition skills. Proc Natl Acad Sci U S A 2014, 111: 1987–1992.PubMedCrossRef Skuse DH, Lori A, Cubells JF, Lee I, Conneely KN, Puura K, et al. Common polymorphism in the oxytocin receptor gene (OXTR) is associated with human social recognition skills. Proc Natl Acad Sci U S A 2014, 111: 1987–1992.PubMedCrossRef
53.
go back to reference Westberg L, Henningsson S, Zettergren A, Svard J, Hovey D, Lin T, et al. Variation in the oxytocin receptor gene is associated with face recognition and its neural correlates. Front Behav Neurosci 2016, 10: 178.PubMedPubMedCentralCrossRef Westberg L, Henningsson S, Zettergren A, Svard J, Hovey D, Lin T, et al. Variation in the oxytocin receptor gene is associated with face recognition and its neural correlates. Front Behav Neurosci 2016, 10: 178.PubMedPubMedCentralCrossRef
54.
go back to reference Uzefovsky F, Shalev I, Israel S, Edelman S, Raz Y, Mankuta D, et al. Oxytocin receptor and vasopressin receptor 1a genes are respectively associated with emotional and cognitive empathy. Horm Behav 2015, 67: 60–65.PubMedCrossRef Uzefovsky F, Shalev I, Israel S, Edelman S, Raz Y, Mankuta D, et al. Oxytocin receptor and vasopressin receptor 1a genes are respectively associated with emotional and cognitive empathy. Horm Behav 2015, 67: 60–65.PubMedCrossRef
55.
go back to reference Weisman O, Pelphrey KA, Leckman JF, Feldman R, Lu Y, Chong A, et al. The association between 2D:4D ratio and cognitive empathy is contingent on a common polymorphism in the oxytocin receptor gene (OXTR rs53576). Psychoneuroendocrinology 2015, 58: 23–32.PubMedCrossRef Weisman O, Pelphrey KA, Leckman JF, Feldman R, Lu Y, Chong A, et al. The association between 2D:4D ratio and cognitive empathy is contingent on a common polymorphism in the oxytocin receptor gene (OXTR rs53576). Psychoneuroendocrinology 2015, 58: 23–32.PubMedCrossRef
56.
go back to reference Tost H, Kolachana B, Hakimi S, Lemaitre H, Verchinski BA, Mattay VS, et al. A common allele in the oxytocin receptor gene (OXTR) impacts prosocial temperament and human hypothalamic-limbic structure and function. Proc Natl Acad Sci U S A 2010, 107: 13936–13941.PubMedPubMedCentralCrossRef Tost H, Kolachana B, Hakimi S, Lemaitre H, Verchinski BA, Mattay VS, et al. A common allele in the oxytocin receptor gene (OXTR) impacts prosocial temperament and human hypothalamic-limbic structure and function. Proc Natl Acad Sci U S A 2010, 107: 13936–13941.PubMedPubMedCentralCrossRef
57.
go back to reference Wang J, Qin W, Liu B, Wang D, Zhang Y, Jiang T, et al. Variant in OXTR gene and functional connectivity of the hypothalamus in normal subjects. Neuroimage 2013, 81: 199–204.PubMedCrossRef Wang J, Qin W, Liu B, Wang D, Zhang Y, Jiang T, et al. Variant in OXTR gene and functional connectivity of the hypothalamus in normal subjects. Neuroimage 2013, 81: 199–204.PubMedCrossRef
58.
go back to reference Schneider-Hassloff H, Straube B, Jansen A, Nuscheler B, Wemken G, Witt SH, et al. Oxytocin receptor polymorphism and childhood social experiences shape adult personality, brain structure and neural correlates of mentalizing. Neuroimage 2016, 134: 671–684.PubMedCrossRef Schneider-Hassloff H, Straube B, Jansen A, Nuscheler B, Wemken G, Witt SH, et al. Oxytocin receptor polymorphism and childhood social experiences shape adult personality, brain structure and neural correlates of mentalizing. Neuroimage 2016, 134: 671–684.PubMedCrossRef
59.
go back to reference Marsh AA, Yu HH, Pine DS, Gorodetsky EK, Goldman D, Blair RJ. The influence of oxytocin administration on responses to infant faces and potential moderation by OXTR genotype. Psychopharmacology (Berl) 2012, 224: 469–476.CrossRef Marsh AA, Yu HH, Pine DS, Gorodetsky EK, Goldman D, Blair RJ. The influence of oxytocin administration on responses to infant faces and potential moderation by OXTR genotype. Psychopharmacology (Berl) 2012, 224: 469–476.CrossRef
60.
go back to reference Feng C, Lori A, Waldman ID, Binder EB, Haroon E, Rilling JK. A common oxytocin receptor gene (OXTR) polymorphism modulates intranasal oxytocin effects on the neural response to social cooperation in humans. Genes Brain Behav 2015, 14: 516–525.PubMedPubMedCentralCrossRef Feng C, Lori A, Waldman ID, Binder EB, Haroon E, Rilling JK. A common oxytocin receptor gene (OXTR) polymorphism modulates intranasal oxytocin effects on the neural response to social cooperation in humans. Genes Brain Behav 2015, 14: 516–525.PubMedPubMedCentralCrossRef
61.
go back to reference King LB, Walum H, Inoue K, Eyrich NW, Young LJ. Variation in the oxytocin receptor gene predicts brain region-specific expression and social attachment. Biol Psychiatry 2016, 80: 160–169.PubMedCrossRef King LB, Walum H, Inoue K, Eyrich NW, Young LJ. Variation in the oxytocin receptor gene predicts brain region-specific expression and social attachment. Biol Psychiatry 2016, 80: 160–169.PubMedCrossRef
62.
go back to reference Lopatina O, Liu HX, Amina S, Hashii M, Higashida H. Oxytocin-induced elevation of ADP-ribosyl cyclase activity, cyclic ADP-ribose or Ca(2+) concentrations is involved in autoregulation of oxytocin secretion in the hypothalamus and posterior pituitary in male mice. Neuropharmacology 2010, 58: 50–55.PubMedCrossRef Lopatina O, Liu HX, Amina S, Hashii M, Higashida H. Oxytocin-induced elevation of ADP-ribosyl cyclase activity, cyclic ADP-ribose or Ca(2+) concentrations is involved in autoregulation of oxytocin secretion in the hypothalamus and posterior pituitary in male mice. Neuropharmacology 2010, 58: 50–55.PubMedCrossRef
63.
go back to reference Liu HX, Lopatina O, Higashida C, Tsuji T, Kato I, Takasawa S, et al. Locomotor activity, ultrasonic vocalization and oxytocin levels in infant CD38 knockout mice. Neurosci Lett 2008, 448: 67–70.PubMedCrossRef Liu HX, Lopatina O, Higashida C, Tsuji T, Kato I, Takasawa S, et al. Locomotor activity, ultrasonic vocalization and oxytocin levels in infant CD38 knockout mice. Neurosci Lett 2008, 448: 67–70.PubMedCrossRef
64.
go back to reference Higashida H, Yokoyama S, Kikuchi M, Munesue T. CD38 and its role in oxytocin secretion and social behavior. Horm Behav 2012, 61: 351–358.PubMedCrossRef Higashida H, Yokoyama S, Kikuchi M, Munesue T. CD38 and its role in oxytocin secretion and social behavior. Horm Behav 2012, 61: 351–358.PubMedCrossRef
65.
go back to reference Higashida H, Yokoyama S, Munesue T, Kikuchi M, Minabe Y, Lopatina O. CD38 gene knockout juvenile mice: a model of oxytocin signal defects in autism. Biol Pharm Bull 2011, 34: 1369–1372.PubMedCrossRef Higashida H, Yokoyama S, Munesue T, Kikuchi M, Minabe Y, Lopatina O. CD38 gene knockout juvenile mice: a model of oxytocin signal defects in autism. Biol Pharm Bull 2011, 34: 1369–1372.PubMedCrossRef
66.
go back to reference Munesue T, Yokoyama S, Nakamura K, Anitha A, Yamada K, Hayashi K, et al. Two genetic variants of CD38 in subjects with autism spectrum disorder and controls. Neurosci Res 2010, 67: 181–191.PubMedCrossRef Munesue T, Yokoyama S, Nakamura K, Anitha A, Yamada K, Hayashi K, et al. Two genetic variants of CD38 in subjects with autism spectrum disorder and controls. Neurosci Res 2010, 67: 181–191.PubMedCrossRef
67.
go back to reference Feldman R, Zagoory-Sharon O, Weisman O, Schneiderman I, Gordon I, Maoz R, et al. Sensitive parenting is associated with plasma oxytocin and polymorphisms in the OXTR and CD38 genes. Biol Psychiatry 2012, 72: 175–181.PubMedCrossRef Feldman R, Zagoory-Sharon O, Weisman O, Schneiderman I, Gordon I, Maoz R, et al. Sensitive parenting is associated with plasma oxytocin and polymorphisms in the OXTR and CD38 genes. Biol Psychiatry 2012, 72: 175–181.PubMedCrossRef
68.
go back to reference Feldman R, Gordon I, Influs M, Gutbir T, Ebstein RP. Parental oxytocin and early caregiving jointly shape children’s oxytocin response and social reciprocity. Neuropsychopharmacology 2013, 38: 1154–1162.PubMedPubMedCentralCrossRef Feldman R, Gordon I, Influs M, Gutbir T, Ebstein RP. Parental oxytocin and early caregiving jointly shape children’s oxytocin response and social reciprocity. Neuropsychopharmacology 2013, 38: 1154–1162.PubMedPubMedCentralCrossRef
69.
go back to reference Ferrero E, Malavasi F. A natural history of the human CD38 gene. In: Lee HC (Ed.). Cyclic ADP-Ribose and NAADP. Structures, Metabolism and Functions. Dordrecht: Kluwer, 2002: 65–79.CrossRef Ferrero E, Malavasi F. A natural history of the human CD38 gene. In: Lee HC (Ed.). Cyclic ADP-Ribose and NAADP. Structures, Metabolism and Functions. Dordrecht: Kluwer, 2002: 65–79.CrossRef
70.
go back to reference Ceroni F, Sagar A, Simpson NH, Gawthrope AJ, Newbury DF, Pinto D, et al. A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma. Autism Res 2014, 7: 254–263.PubMedPubMedCentralCrossRef Ceroni F, Sagar A, Simpson NH, Gawthrope AJ, Newbury DF, Pinto D, et al. A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma. Autism Res 2014, 7: 254–263.PubMedPubMedCentralCrossRef
71.
go back to reference Riebold M, Mankuta D, Lerer E, Israel S, Zhong S, Nemanov L, et al. All-trans retinoic acid upregulates reduced CD38 transcription in lymphoblastoid cell lines from Autism spectrum disorder. Mol Med 2011, 17: 799–806.PubMedPubMedCentralCrossRef Riebold M, Mankuta D, Lerer E, Israel S, Zhong S, Nemanov L, et al. All-trans retinoic acid upregulates reduced CD38 transcription in lymphoblastoid cell lines from Autism spectrum disorder. Mol Med 2011, 17: 799–806.PubMedPubMedCentralCrossRef
72.
go back to reference Kim SJ, Young LJ, Gonen D, Veenstra-VanderWeele J, Courchesne R, Courchesne E, et al. Transmission disequilibrium testing of arginine vasopressin receptor 1A (AVPR1A) polymorphisms in autism. Mol Psychiatry 2002, 7: 503–507.PubMedCrossRef Kim SJ, Young LJ, Gonen D, Veenstra-VanderWeele J, Courchesne R, Courchesne E, et al. Transmission disequilibrium testing of arginine vasopressin receptor 1A (AVPR1A) polymorphisms in autism. Mol Psychiatry 2002, 7: 503–507.PubMedCrossRef
73.
go back to reference Yirmiya N, Rosenberg C, Levi S, Salomon S, Shulman C, Nemanov L, et al. Association between the arginine vasopressin 1a receptor (AVPR1a) gene and autism in a family-based study: mediation by socialization skills. Mol Psychiatry 2006, 11: 488–494.PubMedCrossRef Yirmiya N, Rosenberg C, Levi S, Salomon S, Shulman C, Nemanov L, et al. Association between the arginine vasopressin 1a receptor (AVPR1a) gene and autism in a family-based study: mediation by socialization skills. Mol Psychiatry 2006, 11: 488–494.PubMedCrossRef
74.
go back to reference Yang SY, Cho SC, Yoo HJ, Cho IH, Park M, Yoe J, et al. Family-based association study of microsatellites in the 5′ flanking region of AVPR1A with autism spectrum disorder in the Korean population. Psychiatry Res 2010, 178: 199–201.PubMedCrossRef Yang SY, Cho SC, Yoo HJ, Cho IH, Park M, Yoe J, et al. Family-based association study of microsatellites in the 5′ flanking region of AVPR1A with autism spectrum disorder in the Korean population. Psychiatry Res 2010, 178: 199–201.PubMedCrossRef
75.
go back to reference Tansey KE, Hill MJ, Cochrane LE, Gill M, Anney RJ, Gallagher L. Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism. Mol Autism 2011, 2: 3.PubMedPubMedCentralCrossRef Tansey KE, Hill MJ, Cochrane LE, Gill M, Anney RJ, Gallagher L. Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism. Mol Autism 2011, 2: 3.PubMedPubMedCentralCrossRef
76.
go back to reference Kantojarvi K, Oikkonen J, Kotala I, Kallela J, Vanhala R, Onkamo P, et al. Association and promoter analysis of AVPR1A in finnish autism families. Autism Res 2015, 8: 634–639.PubMedCrossRef Kantojarvi K, Oikkonen J, Kotala I, Kallela J, Vanhala R, Onkamo P, et al. Association and promoter analysis of AVPR1A in finnish autism families. Autism Res 2015, 8: 634–639.PubMedCrossRef
77.
go back to reference Barbosa AC, Kim MS, Ertunc M, Adachi M, Nelson ED, McAnally J, et al. MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function. Proc Natl Acad Sci U S A 2008, 105: 9391–9396.PubMedPubMedCentralCrossRef Barbosa AC, Kim MS, Ertunc M, Adachi M, Nelson ED, McAnally J, et al. MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function. Proc Natl Acad Sci U S A 2008, 105: 9391–9396.PubMedPubMedCentralCrossRef
78.
go back to reference Francis SM, Kim SJ, Kistner-Griffin E, Guter S, Cook EH, Jacob S. ASD and genetic associations with receptors for oxytocin and vasopressin-AVPR1A, AVPR1B, and OXTR. Front Neurosci 2016, 10: 516.PubMedPubMedCentral Francis SM, Kim SJ, Kistner-Griffin E, Guter S, Cook EH, Jacob S. ASD and genetic associations with receptors for oxytocin and vasopressin-AVPR1A, AVPR1B, and OXTR. Front Neurosci 2016, 10: 516.PubMedPubMedCentral
79.
go back to reference Bielsky IF, Hu SB, Szegda KL, Westphal H, Young LJ. Profound impairment in social recognition and reduction in anxiety-like behavior in vasopressin V1a receptor knockout mice. Neuropsychopharmacology 2004, 29: 483–493.PubMedCrossRef Bielsky IF, Hu SB, Szegda KL, Westphal H, Young LJ. Profound impairment in social recognition and reduction in anxiety-like behavior in vasopressin V1a receptor knockout mice. Neuropsychopharmacology 2004, 29: 483–493.PubMedCrossRef
80.
go back to reference Mabry KE, Streatfeild CA, Keane B, Solomon NG. avpr1a length polymorphism is not associated with either social or genetic monogamy in free-living prairie voles. Anim Behav 2011, 81: 11–18.PubMedPubMedCentralCrossRef Mabry KE, Streatfeild CA, Keane B, Solomon NG. avpr1a length polymorphism is not associated with either social or genetic monogamy in free-living prairie voles. Anim Behav 2011, 81: 11–18.PubMedPubMedCentralCrossRef
81.
go back to reference Hammock EA, Young LJ. Microsatellite instability generates diversity in brain and sociobehavioral traits. Science 2005, 308: 1630–1634.PubMedCrossRef Hammock EA, Young LJ. Microsatellite instability generates diversity in brain and sociobehavioral traits. Science 2005, 308: 1630–1634.PubMedCrossRef
82.
go back to reference Knafo A, Israel S, Darvasi A, Bachner-Melman R, Uzefovsky F, Cohen L, et al. Individual differences in allocation of funds in the dictator game associated with length of the arginine vasopressin 1a receptor RS3 promoter region and correlation between RS3 length and hippocampal mRNA. Genes Brain Behav 2008, 7: 266–275.PubMedCrossRef Knafo A, Israel S, Darvasi A, Bachner-Melman R, Uzefovsky F, Cohen L, et al. Individual differences in allocation of funds in the dictator game associated with length of the arginine vasopressin 1a receptor RS3 promoter region and correlation between RS3 length and hippocampal mRNA. Genes Brain Behav 2008, 7: 266–275.PubMedCrossRef
83.
go back to reference Levin R, Heresco-Levy U, Bachner-Melman R, Israel S, Shalev I, Ebstein RP. Association between arginine vasopressin 1a receptor (AVPR1a) promoter region polymorphisms and prepulse inhibition. Psychoneuroendocrinology 2009, 34: 901–908.PubMedCrossRef Levin R, Heresco-Levy U, Bachner-Melman R, Israel S, Shalev I, Ebstein RP. Association between arginine vasopressin 1a receptor (AVPR1a) promoter region polymorphisms and prepulse inhibition. Psychoneuroendocrinology 2009, 34: 901–908.PubMedCrossRef
84.
go back to reference Liu JJ, Lou F, Lavebratt C, Forsell Y. Impact of childhood adversity and vasopressin receptor 1a variation on social interaction in adulthood: a cross-sectional study. PLoS One 2015, 10: e0136436.PubMedPubMedCentralCrossRef Liu JJ, Lou F, Lavebratt C, Forsell Y. Impact of childhood adversity and vasopressin receptor 1a variation on social interaction in adulthood: a cross-sectional study. PLoS One 2015, 10: e0136436.PubMedPubMedCentralCrossRef
85.
go back to reference Walum H, Westberg L, Henningsson S, Neiderhiser JM, Reiss D, Igl W, et al. Genetic variation in the vasopressin receptor 1a gene (AVPR1A) associates with pair-bonding behavior in humans. Proc Natl Acad Sci U S A 2008, 105: 14153–14156.PubMedPubMedCentralCrossRef Walum H, Westberg L, Henningsson S, Neiderhiser JM, Reiss D, Igl W, et al. Genetic variation in the vasopressin receptor 1a gene (AVPR1A) associates with pair-bonding behavior in humans. Proc Natl Acad Sci U S A 2008, 105: 14153–14156.PubMedPubMedCentralCrossRef
86.
go back to reference Krueger F, Parasuraman R, Iyengar V, Thornburg M, Weel J, Lin M, et al. Oxytocin receptor genetic variation promotes human trust behavior. Front Hum Neurosci 2012, 6: 4.PubMedPubMedCentral Krueger F, Parasuraman R, Iyengar V, Thornburg M, Weel J, Lin M, et al. Oxytocin receptor genetic variation promotes human trust behavior. Front Hum Neurosci 2012, 6: 4.PubMedPubMedCentral
87.
go back to reference Procyshyn TL, Hurd PL, Crespi BJ. Association testing of vasopressin receptor 1a microsatellite polymorphisms in non-clinical autism spectrum phenotypes. Autism Res 2016. doi:10.1002/aur.1716.PubMed Procyshyn TL, Hurd PL, Crespi BJ. Association testing of vasopressin receptor 1a microsatellite polymorphisms in non-clinical autism spectrum phenotypes. Autism Res 2016. doi:10.​1002/​aur.​1716.PubMed
88.
go back to reference Neumann ID, Slattery DA. Oxytocin in General Anxiety and Social Fear: A Translational Approach. Biol Psychiatry 2016, 79: 213–221.PubMedCrossRef Neumann ID, Slattery DA. Oxytocin in General Anxiety and Social Fear: A Translational Approach. Biol Psychiatry 2016, 79: 213–221.PubMedCrossRef
89.
go back to reference Anagnostou E, Soorya L, Brian J, Dupuis A, Mankad D, Smile S, et al. Intranasal oxytocin in the treatment of autism spectrum disorders: a review of literature and early safety and efficacy data in youth. Brain Res 2014, 1580: 188–198.PubMedCrossRef Anagnostou E, Soorya L, Brian J, Dupuis A, Mankad D, Smile S, et al. Intranasal oxytocin in the treatment of autism spectrum disorders: a review of literature and early safety and efficacy data in youth. Brain Res 2014, 1580: 188–198.PubMedCrossRef
90.
go back to reference Guastella AJ, Hickie IB. Oxytocin treatment, circuitry and autism: a critical review of the literature placing oxytocin into the autism context. Biol Psychiatry 2016, 79: 234–242.PubMedCrossRef Guastella AJ, Hickie IB. Oxytocin treatment, circuitry and autism: a critical review of the literature placing oxytocin into the autism context. Biol Psychiatry 2016, 79: 234–242.PubMedCrossRef
91.
go back to reference Gumley A, Braehler C, Macbeth A. A meta-analysis and theoretical critique of oxytocin and psychosis: prospects for attachment and compassion in promoting recovery. Br J Clin Psychol 2014, 53: 42–61.PubMedCrossRef Gumley A, Braehler C, Macbeth A. A meta-analysis and theoretical critique of oxytocin and psychosis: prospects for attachment and compassion in promoting recovery. Br J Clin Psychol 2014, 53: 42–61.PubMedCrossRef
92.
go back to reference Bartz JA, Hollander E. Oxytocin and experimental therapeutics in autism spectrum disorders. Prog Brain Res 2008, 170: 451–462.PubMedCrossRef Bartz JA, Hollander E. Oxytocin and experimental therapeutics in autism spectrum disorders. Prog Brain Res 2008, 170: 451–462.PubMedCrossRef
93.
go back to reference Macdonald K, Macdonald TM. The peptide that binds: a systematic review of oxytocin and its prosocial effects in humans. Harv Rev Psychiatry 2010, 18: 1–21.PubMedCrossRef Macdonald K, Macdonald TM. The peptide that binds: a systematic review of oxytocin and its prosocial effects in humans. Harv Rev Psychiatry 2010, 18: 1–21.PubMedCrossRef
94.
go back to reference Andari E, Duhamel JR, Zalla T, Herbrecht E, Leboyer M, Sirigu A. Promoting social behavior with oxytocin in high-functioning autism spectrum disorders. Proc Natl Acad Sci U S A 2010, 107: 4389–4394.PubMedPubMedCentralCrossRef Andari E, Duhamel JR, Zalla T, Herbrecht E, Leboyer M, Sirigu A. Promoting social behavior with oxytocin in high-functioning autism spectrum disorders. Proc Natl Acad Sci U S A 2010, 107: 4389–4394.PubMedPubMedCentralCrossRef
95.
go back to reference Yatawara CJ, Einfeld SL, Hickie IB, Davenport TA, Guastella AJ. The effect of oxytocin nasal spray on social interaction deficits observed in young children with autism: a randomized clinical crossover trial. Mol Psychiatry 2016, 21: 1225–1231.PubMedCrossRef Yatawara CJ, Einfeld SL, Hickie IB, Davenport TA, Guastella AJ. The effect of oxytocin nasal spray on social interaction deficits observed in young children with autism: a randomized clinical crossover trial. Mol Psychiatry 2016, 21: 1225–1231.PubMedCrossRef
96.
go back to reference Kosaka H, Munesue T, Ishitobi M, Asano M, Omori M, Sato M, et al. Long-term oxytocin administration improves social behaviors in a girl with autistic disorder. BMC Psychiatry 2012, 12: 110.PubMedPubMedCentralCrossRef Kosaka H, Munesue T, Ishitobi M, Asano M, Omori M, Sato M, et al. Long-term oxytocin administration improves social behaviors in a girl with autistic disorder. BMC Psychiatry 2012, 12: 110.PubMedPubMedCentralCrossRef
97.
go back to reference Watanabe T, Kuroda M, Kuwabara H, Aoki Y, Iwashiro N, Tatsunobu N, et al. Clinical and neural effects of six-week administration of oxytocin on core symptoms of autism. Brain 2015, 138: 3400–3412.PubMedCrossRef Watanabe T, Kuroda M, Kuwabara H, Aoki Y, Iwashiro N, Tatsunobu N, et al. Clinical and neural effects of six-week administration of oxytocin on core symptoms of autism. Brain 2015, 138: 3400–3412.PubMedCrossRef
98.
go back to reference Gordon I, Jack A, Pretzsch CM, Vander Wyk B, Leckman JF, Feldman R, et al. Intranasal oxytocin enhances connectivity in the neural circuitry supporting social motivation and social perception in children with autism. Sci Rep 2016, 6: 35054.PubMedPubMedCentralCrossRef Gordon I, Jack A, Pretzsch CM, Vander Wyk B, Leckman JF, Feldman R, et al. Intranasal oxytocin enhances connectivity in the neural circuitry supporting social motivation and social perception in children with autism. Sci Rep 2016, 6: 35054.PubMedPubMedCentralCrossRef
99.
go back to reference Dadds MR, MacDonald E, Cauchi A, Williams K, Levy F, Brennan J. Nasal oxytocin for social deficits in childhood autism: a randomized controlled trial. J Autism Dev Disord 2014, 44: 521–531.PubMedCrossRef Dadds MR, MacDonald E, Cauchi A, Williams K, Levy F, Brennan J. Nasal oxytocin for social deficits in childhood autism: a randomized controlled trial. J Autism Dev Disord 2014, 44: 521–531.PubMedCrossRef
100.
go back to reference Guastella AJ, Gray KM, Rinehart NJ, Alvares GA, Tonge BJ, Hickie IB, et al. The effects of a course of intranasal oxytocin on social behaviors in youth diagnosed with autism spectrum disorders: a randomized controlled trial. J Child Psychol Psychiatry 2015, 56: 444–452.PubMedCrossRef Guastella AJ, Gray KM, Rinehart NJ, Alvares GA, Tonge BJ, Hickie IB, et al. The effects of a course of intranasal oxytocin on social behaviors in youth diagnosed with autism spectrum disorders: a randomized controlled trial. J Child Psychol Psychiatry 2015, 56: 444–452.PubMedCrossRef
101.
go back to reference Kosaka H, Okamoto Y, Munesue T, Yamasue H, Inohara K, Fujioka T, et al. Oxytocin efficacy is modulated by dosage and oxytocin receptor genotype in young adults with high-functioning autism: a 24-week randomized clinical trial. Transl Psychiatry 2016, 6: e872.PubMedPubMedCentralCrossRef Kosaka H, Okamoto Y, Munesue T, Yamasue H, Inohara K, Fujioka T, et al. Oxytocin efficacy is modulated by dosage and oxytocin receptor genotype in young adults with high-functioning autism: a 24-week randomized clinical trial. Transl Psychiatry 2016, 6: e872.PubMedPubMedCentralCrossRef
102.
go back to reference Okamoto Y, Ishitobi M, Wada Y, Kosaka H. The potential of nasal oxytocin administration for remediation of autism spectrum disorders. CNS Neurol Disord Drug Targets 2016, 15: 564–577.PubMedPubMedCentralCrossRef Okamoto Y, Ishitobi M, Wada Y, Kosaka H. The potential of nasal oxytocin administration for remediation of autism spectrum disorders. CNS Neurol Disord Drug Targets 2016, 15: 564–577.PubMedPubMedCentralCrossRef
103.
go back to reference Wang H, Duclot F, Liu Y, Wang Z, Kabbaj M. Histone deacetylase inhibitors facilitate partner preference formation in female prairie voles. Nat Neurosci 2013, 16: 919–924.PubMedPubMedCentralCrossRef Wang H, Duclot F, Liu Y, Wang Z, Kabbaj M. Histone deacetylase inhibitors facilitate partner preference formation in female prairie voles. Nat Neurosci 2013, 16: 919–924.PubMedPubMedCentralCrossRef
104.
go back to reference Harony-Nicolas H, Mamrut S, Brodsky L, Shahar-Gold H, Barki-Harrington L, Wagner S. Brain region-specific methylation in the promoter of the murine oxytocin receptor gene is involved in its expression regulation. Psychoneuroendocrinology 2014, 39: 121–131.PubMedCrossRef Harony-Nicolas H, Mamrut S, Brodsky L, Shahar-Gold H, Barki-Harrington L, Wagner S. Brain region-specific methylation in the promoter of the murine oxytocin receptor gene is involved in its expression regulation. Psychoneuroendocrinology 2014, 39: 121–131.PubMedCrossRef
105.
go back to reference Bakermans-Kranenburg MJ, van Ijzendoorn MH. A sociability gene? Meta-analysis of oxytocin receptor genotype effects in humans. Psychiatr Genet 2014, 24: 45–51.PubMedCrossRef Bakermans-Kranenburg MJ, van Ijzendoorn MH. A sociability gene? Meta-analysis of oxytocin receptor genotype effects in humans. Psychiatr Genet 2014, 24: 45–51.PubMedCrossRef
Metadata
Title
Genes Related to Oxytocin and Arginine-Vasopressin Pathways: Associations with Autism Spectrum Disorders
Authors
Rong Zhang
Hong-Feng Zhang
Ji-Sheng Han
Song-Ping Han
Publication date
01-04-2017
Publisher
Springer Singapore
Published in
Neuroscience Bulletin / Issue 2/2017
Print ISSN: 1673-7067
Electronic ISSN: 1995-8218
DOI
https://doi.org/10.1007/s12264-017-0120-7

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