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Oxytocin, brain physiology, and functional connectivity: A review of intranasal oxytocin fMRI studies

期刊

PSYCHONEUROENDOCRINOLOGY
卷 38, 期 7, 页码 962-974

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.psyneuen.2012.10.011

关键词

Oxytocin; fMRI; Amygdala; Functional connectivity; Neural communication; Social brain

资金

  1. Netherlands Society of Scientific Research [056-24-010]
  2. MRC UK
  3. Wellcome Trust
  4. Autism Research Trust
  5. Medical Research Council [G0600977] Funding Source: researchfish
  6. MRC [G0600977] Funding Source: UKRI

向作者/读者索取更多资源

In recent years the neuropeptide oxytocin (OT) has become one of the most studied peptides of the human neuroendocrine system. Research has shown widespread behavioural effects and numerous potential therapeutic benefits. However, little is known about how OT triggers these effects in the brain. Here, we discuss some of the physiological properties of OT in the human brain including the long half-life of neuropeptides, the diffuse projections of OT throughout the brain and interactions with other systems such as the dopaminergic system. These properties indicate that OT acts without clear spatial and temporal specificity. Therefore, it is Likely to have widespread effects on the brain's intrinsic functioning. Additionally, we review studies that have used functional magnetic resonance imaging (fMRI) concurrently with OT administration. These studies reveal a specific set of 'social' brain regions that are likely to be the strongest targets for OT's potential to influence human behaviour. On the basis of the fMRI literature and the physiological properties of the neuropeptide, we argue that OT has the potential to not only modulate activity in a set of specific brain regions, but also the functional connectivity between these regions. In light of the increasing knowledge of the behavioural effects of OT in humans, studies of the effects of OT administration on brain function can contribute to our understanding of the neural networks in the social brain. (C) 2012 Elsevier Ltd. All rights reserved.

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