Oxytocin and experimental therapeutics in autism spectrum disorders

被引:99
作者
Bartz, Jennifer A. [1 ]
Hollander, Eric [1 ]
机构
[1] Mt Sinai Sch Med, New York, NY 10029 USA
来源
ADVANCES IN VASOPRESSIN AND OXYTOCIN: FROM GENES TO BEHAVIOUR TO DISEASE | 2008年 / 170卷
关键词
autism spectrum disorders; oxytocin; vasopressin; experimental therapeutics; treatment; social functioning; social cognition; repetitive behaviours; RECEPTOR GENE-EXPRESSION; SOCIAL RECOGNITION; MATERNAL-BEHAVIOR; VASOPRESSIN RECEPTOR; SPECIES-DIFFERENCES; PARTNER PREFERENCE; ASPERGER-SYNDROME; FACE PERCEPTION; NORMAL ADULTS; FEMALE;
D O I
10.1016/S0079-6123(08)00435-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Autism is a developmental disorder characterized by three core symptom domains: speech and communication abnormalities, social functioning impairments and repetitive behaviours and restricted interests. Oxytocin (OXT) is a nine-amino-acid peptide that is synthesized in the paraventricular and supraoptic nucleus of the hypothalamus and released into the bloodstream by axon terminals in the posterior pituitary where it plays an important role in facilitating uterine contractions during parturition and in milk let-down. In addition, OXT and the structurally similar peptide arginine vasopressin (AVP) are released within the brain where they play a key role in regulating affiliative behaviours, including sexual behaviour, mother-infant and adult-adult pair-bond formation and social memory/recognition. Finally, OXT has been implicated in repetitive behaviours and stress reactivity. Given that OXT is involved in the regulation of repetitive and affiliative behaviours, and that these are key features of autism, it is believed that OXT may play a role in autism and that OXT may be an effective treatment for these two core symptom domains. In this chapter we review evidence to date supporting a relationship between OXT and autism; we then discuss research looking at the functional role of OXT in autism, as well as a pilot study investigating the therapeutic efficacy of OXT in treating core autism symptom domains. Finally, we conclude with a discussion of directions for future research.
引用
收藏
页码:451 / 462
页数:12
相关论文
共 84 条
[71]   Reading the mind in the voice: A study with normal adults and adults with Asperger syndrome and high functioning autism [J].
Rutherford, MD ;
Baron-Cohen, S ;
Wheelwright, S .
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 2002, 32 (03) :189-194
[72]  
SOFRONIEW MV, 1983, PROG BRAIN RES, V60, P101
[73]   ASPERGERS SYNDROME AND AUTISM - NEUROCOGNITIVE ASPECTS [J].
SZATMARI, P ;
TUFF, L ;
FINLAYSON, AJ ;
BARTOLUCCI, G .
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 1990, 29 (01) :130-136
[74]   AUTISTIC CHILDRENS ABILITY TO INTERPRET FACES - A RESEARCH NOTE [J].
TANTAM, D ;
MONAGHAN, L ;
NICHOLSON, H ;
STIRLING, J .
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES, 1989, 30 (04) :623-630
[75]  
Wang ZX, 1996, J COMP NEUROL, V366, P726
[76]   Examination of AVPR1a as an autism susceptibility gene [J].
Wassink, TH ;
Piven, J ;
Vieland, VJ ;
Pietila, J ;
Goedken, RJ ;
Folstein, SE ;
Sheffield, VC .
MOLECULAR PSYCHIATRY, 2004, 9 (10) :968-972
[77]   Neurofunctional mechanisms in autism [J].
Waterhouse, L ;
Fein, D ;
Modahl, C .
PSYCHOLOGICAL REVIEW, 1996, 103 (03) :457-489
[78]   OXYTOCIN ADMINISTERED CENTRALLY FACILITATES FORMATION OF A PARTNER PREFERENCE IN FEMALE PRAIRIE VOTES (MICROTUS-OCHROGASTER) [J].
WILLIAMS, JR ;
INSEL, TR ;
HARBAUGH, CR ;
CARTER, CS .
JOURNAL OF NEUROENDOCRINOLOGY, 1994, 6 (03) :247-250
[79]   Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population [J].
Wu, SP ;
Jia, MX ;
Ruan, Y ;
Liu, J ;
Guo, YQ ;
Shuang, M ;
Gong, XH ;
Zhang, YB ;
Yang, XL ;
Zhang, D .
BIOLOGICAL PSYCHIATRY, 2005, 58 (01) :74-77
[80]   Association between the arginine vasopressin 1a receptor (AVPR1a) gene and autism in a family-based study:: mediation by socialization skills [J].
Yirmiya, N ;
Rosenberg, C ;
Levi, S ;
Salomon, S ;
Shulman, C ;
Nemanov, L ;
Dina, C ;
Ebstein, RP .
MOLECULAR PSYCHIATRY, 2006, 11 (05) :488-494