Prenatal alcohol exposure retards the migration and development of serotonin neurons in fetal C57BL mice

Citation
Fc. Zhou et al., Prenatal alcohol exposure retards the migration and development of serotonin neurons in fetal C57BL mice, DEV BRAIN R, 126(2), 2001, pp. 147-155
Citations number
44
Categorie Soggetti
Neurosciences & Behavoir
Journal title
DEVELOPMENTAL BRAIN RESEARCH
ISSN journal
01653806 → ACNP
Volume
126
Issue
2
Year of publication
2001
Pages
147 - 155
Database
ISI
SICI code
0165-3806(20010228)126:2<147:PAERTM>2.0.ZU;2-S
Abstract
Incomplete neural tube fusion (iNTF), induced by alcohol, in midline floor and roof plates was found in our recent study. In this study, serotonin (5- HT) neurons, known to be born entirely in the midline raphe at brainstem, w ere examined during their development with fetal alcohol exposure. Weight-m atched C57BL mice pregnant darns were divided into three groups on E8: one received ethanol via a chocolate Sustacal liquid diet providing 20% ethanol -derived calories as the sole source of nutrients (ALC); the second receive d an isocaloric Sustacal liquid diet and was pair-fed to individual dams in the ethanol-fed group (PF); the third was fed ad lib rat chow (Chow). Feta l brains were obtained on E15 and were processed for immunostaining of 5-HT and its trophic factor, S100 beta. The ascending 5-HT neurons, in normal d evelopment, appear bilaterally near midline on E12, and by E15, as seen in chow and PF groups, migrate from the midline germinal zone laterally and do rsally to their final position with rich fibers. In contrast, in the E15 AL C group, many 5-HT-im neurons were found remaining in the midline germinal region or had migrated, but with under-differentiated, sparse fibers. There were 20-30% fewer 5-HT-im neurons in ALC as compared to PF and Chow. In ad dition, the number of S100 beta cells was less in ALC as compared with PF a nd Chow groups. No difference was found between PF and Chow in number of 5- HT-im or S100 beta -im cells. The 5-HT neurons found compromised in migrati on and differentiation may, in parr, stem from failure of access to floor p late or midline tissue induction and the insufficient support by S100 beta. As 5-HT neurons have been implicated for signaling brain maturation, fewer 5-HT neurons may have lasting effects on the development of brain or, if p ersistent in the adult, profoundly affect adult brain function. (C) 2001 El sevier Science B.V. All rights reserved.