2′3′cyclic nucleotide 3′phosphodiesterase immunohistochemistry shows an impairment on myelin compaction in hypothyroid rats

The effects of hypothyroidism on oligodendroglial differentiation and myelination are for the first time studied by immunohistochemical localization of an early oligodendroglial marker, the 2′3′cyclic nucleotide 3′phosphodiesterase (E.C. 3.1.4.37‐CNPase), in developing rats. Two groups received meth...

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Bibliographic Details
Published in:International journal of developmental neuroscience Vol. 18; no. 8; pp. 887 - 892
Main Authors: Barradas, Penha C., Ferraz, Alessandra S., Ferreira, Andréa A., Daumas, Regina P., Moura, Egberto G.
Format: Journal Article
Language:English
Published: 01-12-2000
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Summary:The effects of hypothyroidism on oligodendroglial differentiation and myelination are for the first time studied by immunohistochemical localization of an early oligodendroglial marker, the 2′3′cyclic nucleotide 3′phosphodiesterase (E.C. 3.1.4.37‐CNPase), in developing rats. Two groups received methimazol; one during gestation (H) and another postnatally (PN). One H sub‐group received thyroxine after birth (T). We observed a delay in CNPase expression followed by a decrease in the number of CNPase immunoreactive fibers in both H and PN groups. The T sub‐group was not different from controls. Furthermore, the immunoreactive fibers, in mature hypothyroid animals, showed a continuous pattern of staining in contrast with a discontinuous one in controls. Myelinogenesis is a highly regulated timed event. CNPase links myelin related proteins to the cytoskeleton also interacting with membrane lipids during extension and wrapping of the oligodendroglial process around the axon (ensheathment phase). In mature myelinated fiber the CNPase is absent from compact myelin sheath, being located only in the inner and outer loops and in paranodal loops. Thus, our data suggest a disorder in myelin compaction and point once more to the post‐natal period as critical for the mechanisms that are thyroid hormone regulated in myelinogenesis.
ISSN:0736-5748
1873-474X
DOI:10.1016/S0736-5748(00)00028-9