Literature DB >> 25748751

The myelinated fiber loss in the corpus callosum of mouse model of schizophrenia induced by MK-801.

Yun Xiu1, Xiang-ru Kong2, Lei Zhang3, Xuan Qiu3, Yuan Gao4, Chun-xia Huang5, Feng-lei Chao3, San-rong Wang3, Yong Tang6.   

Abstract

Previous magnetic resonance imaging (MRI) and diffusion tensor imaging (DTI) investigations have shown that the white matter volume and fractional anisotropy (FA) were decreased in schizophrenia (SZ), which indicated impaired white matter integrity in SZ. However, the mechanism underlying these abnormalities has been less studied. The current study was designed to investigate the possible reasons for white matter abnormalities in the mouse model of SZ induced by NMDA receptor antagonist using the unbiased stereological methods and transmission electron microscope technique. We found that the mice treated with MK-801 demonstrated a series of schizophrenia-like behaviors including hyperlocomotor activity and more anxiety. The myelinated fibers in the corpus callosum (CC) of the mice treated with MK-801 were impaired with splitting lamellae of myelin sheaths and segmental demyelination. The CC volume and the total length of the myelinated fibers in the CC of the mice treated with MK-801 were significantly decreased by 9.4% and 16.8% when compared to those of the mice treated with saline. We further found that the loss of the myelinated fibers length was mainly due to the marked loss of the myelinated nerve fibers with the diameter of 0.4-0.5 μm. These results indicated that the splitting myelin sheaths, demyelination and the loss of myelinated fibers with small diameter might provide one of the structural bases for impaired white matter integrity of CC in the mouse model of SZ. These results might also provide a baseline for further studies searching for the treatment of SZ through targeting white matter.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Corpus callosum; Myelinated fiber; Schizophrenia; Stereology

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Year:  2015        PMID: 25748751     DOI: 10.1016/j.jpsychires.2015.02.013

Source DB:  PubMed          Journal:  J Psychiatr Res        ISSN: 0022-3956            Impact factor:   4.791


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