Skip to main content
Full access
Images in Neuroscience
Published Online: 1 February 1999

Brain Development, X: Pruning During Development

Publication: American Journal of Psychiatry
Human brain size changes little over the child and teen years. Nonetheless, considerable cellular and functional change occurs. These maturational changes result in an adult functioning brain and are subject to developmental influence. The images above serve to illustrate this. Figure A shows that at birth, cellular elements are still entering the cortex. By midchildhood, more neurons and more cellular processes are established than in adult years. The developmental task of childhood years from an anatomic point of view is to prune and to select the most useful (perhaps the most used) neurons, synapses, and dendrites to preserve for the adult brain. This process of pruning continues through the early teen years. Presumably, the pruning is accomplished “wisely.” This would mean that synapses that are most important to survival and optimal function flourish whereas useless connections vanish.
One marker of neuronal number is the density of neurotransmitter receptors. In figure B, the density of the dopamine D2 receptor is graphed over a wide age range, beginning immediately after birth and extending to the ninth decade. This graph illustrates the high density of D2 receptors before 5 years of age, a density greater than adult levels, and their regression to adult levels reached during the second decade. Dopamine receptors continue to decrease in adult years, but at a considerably slower rate of 2.2% reduction per decade. This rate is faster in males than in females. But the decrease is slower overall than the tremendous childhood increase in number. In schizophrenia, the rate of D2 receptor loss is faster than in healthy comparison subjects: a 1.9% loss per decade in comparison men and a 6.0% loss per decade in men with schizophrenia.
These data suggest that while certain fixed processes establish the availability of CNS neurons, other influences generated by the organism and the environment serve to determine neuronal survival and connectivity.
Left Figure
Proliferation and decline in synaptic connections in children
Right Figure
Reproduced from Seeman et al.: Human Brain Dopamine Receptors in Children and Aging Adults. Synapse 1987; 1:399–404. Copyright ” 1987, Wiley-Liss, Inc., a division of John Wiley and Sons, Inc. Reprinted by permission of John Wiley and Sons, Inc.

Footnote

Figure A courtesy of Dr. Seeman.

Information & Authors

Information

Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 168
PubMed: 9989550

History

Published online: 1 February 1999
Published in print: February 1999

Authors

Details

PHILIP SEEMAN, M.D., PH.D.
Toronto, Ont., Canada

Metrics & Citations

Metrics

Citations

Export Citations

If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Simply select your manager software from the list below and click Download.

For more information or tips please see 'Downloading to a citation manager' in the Help menu.

Format
Citation style
Style
Copy to clipboard

View Options

View options

PDF/EPUB

View PDF/EPUB

Get Access

Login options

Already a subscriber? Access your subscription through your login credentials or your institution for full access to this article.

Personal login Institutional Login Open Athens login
Purchase Options

Purchase this article to access the full text.

PPV Articles - American Journal of Psychiatry

PPV Articles - American Journal of Psychiatry

Not a subscriber?

Subscribe Now / Learn More

PsychiatryOnline subscription options offer access to the DSM-5-TR® library, books, journals, CME, and patient resources. This all-in-one virtual library provides psychiatrists and mental health professionals with key resources for diagnosis, treatment, research, and professional development.

Need more help? PsychiatryOnline Customer Service may be reached by emailing [email protected] or by calling 800-368-5777 (in the U.S.) or 703-907-7322 (outside the U.S.).

Media

Figures

Other

Tables

Share

Share

Share article link

Share