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Volume 57, Issue 1, Pages 83-90 (1 January 2005)


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Direct and indirect effects of fetal irradiation on cortical gray and white matter volume in the macaque

Lynn D. SelemonaCorresponding Author Informationemail address, Lei Wangb, Mary Beth Nebelb, John G. Csernanskybc, Patricia S. Goldman-Rakica, Pasko Rakica

Received 10 February 2004; received in revised form 30 August 2004; accepted 5 October 2004.

Background

Schizophrenia is associated with reductions in thalamic neuronal number and cortical gray matter volume. Exposure of nonhuman primates to x-irradiation in early gestation has previously been shown to decrease thalamic volume and neuronal number. Here we examine whether early gestational irradiation also results in cortical volume reduction.

Methods

High-resolution, T1-weighted magnetic resonance scans were collected in adult monkeys 1) exposed to irradiation during the early gestational period (E33-E42) corresponding to thalamic neurogenesis, 2) irradiated in midgestation (E70-81) during neocortical neurogenesis, and 3) not exposed to irradiation. Cortical gray matter and white matter volumes were derived via manual segmentation; frontal and nonfrontal volumes were distinguished via sulcal landmarks.

Results

Monkeys irradiated in early gestation exhibited a trend reduction in nonfrontal gray matter volume (17%) and significant reductions in white matter volume in frontal (26%) and nonfrontal (36%) lobes. Monkeys irradiated in midgestation had smaller gray (frontal: 28%; nonfrontal: 22%) and white matter (frontal: 29%; nonfrontal: 38%) volumes.

Conclusions

The cortical deficits observed in midgestationally irradiated monkeys are consistent with a reduction in cortical neuronal number. Cortical volume reductions following early gestational irradiation may be secondary to reduced thalamic neuronal number and therefore model the thalamocortical pathology of schizophrenia.

a Department of Neurobiology, Yale University School of Medicine, New Haven, Connecticut

b Department of Psychiatry, Washington University School of Medicine, St. Louis, Missouri

c Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, Missouri

Corresponding Author InformationAddress reprint requests to Dr. Lynn D. Selemon, Department of Neurobiology, Yale University School of Medicine, P.O. Box 208001, New Haven, CT 06520-8001

PII: S0006-3223(04)01094-7

doi:10.1016/j.biopsych.2004.10.014


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