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EDITORIAL article

Front. Psychiatry, 23 July 2012
Sec. Child and Adolescent Psychiatry
This article is part of the Research Topic Translational research models and methods for mother-infant interactions and developmental studies View all 32 articles

Translational Research Models and Methods for Mother-Infant Interactions and Developmental Studies

  • The Johns Lab, Departments of Psychiatry and Psychology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA

The disruption of mother-infant interactions can have life-long detrimental consequences for offspring and mothers. Recently, science has begun to emphasize translational research including preclinical and neurobiological research that may have direct implications for clinical populations and issues (see Figure 1) (Watson et al., 2006). This group of papers focuses broadly on translational studies highlighting factors that may affect or alter infant or child development and maternal response capability. Articles, both preclinical and clinical, highlight topics such as drug abuse, maternal neglect, altered reward systems, stress, biological and neural system development, child and infant behavioral development, genetics/epigenetics, intergenerational studies, and logistical issues of comparative measurement. Articles include research methods papers, reviews, original research articles, techniques, and opinion articles that address these topics. New methods papers for comparative measures between clinical and preclinical populations are included. Our aims include introducing new translational models and methods for research through a group of outstanding papers focused on these topics.

FIGURE 1
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Figure 1. Approximate neuro-development comparison in humans (blue) and rats (orange; Watson et al., 2006). 1–6 = Myelination, 1 = myelination onset internal capsule, 2 = onset olfactory tract, 3 = onset anterior commissure, 4 = onset fornix, 5 = 50% myelination of corpus callosum, 6 = mature myelination, 7 = 50% cerebellum size, 8 = peak synaptogenesis period, 9 = maximum brain growth velocity (peak), 10 = cortical dominance established, 11 = mature cerebral metabolism, 12 = adult pattern of slow wave and REM sleep, 13 = adult brain weight, 14 = mature prefrontal cortex.

References

Watson, R. E., DeSesso, J. M., Hurtt, M. E., and Cappon, G. D. (2006). Postnatal growth and morphological development of the brain: a species comparison. Birth Defects Res. B Dev. Reprod. Toxicol. 77, 471–484.

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Citation: Johns J (2012) Translational research models and methods for mother-infant interactions and developmental studies. Front. Psychiatry 3:68. doi: 10.3389/fpsyt.2012.00068

Received: 12 March 2012; Accepted: 26 June 2012;
Published online: 23 July 2012.

Edited by:

Vishal Madaan, University of Virginia Health System, USA

Copyright: © 2012 Johns. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

*Correspondence: jjohns@med.unc.edu

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