Literature DB >> 7418632

Cerebellar granule cell genesis in the hydrocortisone-treated rats.

M C Bohn, J M Lauder.   

Abstract

The development of the cerebellar cortex was studied by quantitative light microscopic methods in rats treated with hydrocortisone on postnatal days 7-18. This treatment resulted in a decreased number of cells in the external granular layer (EGL) and an early disappearance of the EGL. In the adult cerebellum of these neonatally treated animals, the total number of granule cells in lobule VIII was decreased by 41% and that of molecular layer microneurons by 28%. Autoradiographic determinations of the 'birthdays' (time of origin) of cerebellar microneurons showed that the peaks of cell formation in the internal granular and molecular layers occurred at earlier ages than in controls. In the granule cell population, this observation was the result of both decreased cell proliferation during the treatment and premature cessation of division in granule cell precursors in the EGL. The morphological effects of 'late' hydrocortisone treatment on the cerebellum observed in this study are compared with those of 'early' hydrocortisone treatment on days 1-4 and those of thyroid hormone from previous studies. It is suggested that endogenous levels of both thyroid and glucocorticoid hormones during the neonatal period may influence the rate of neurogenesis in the postnatal rat cerebellum.

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Year:  1980        PMID: 7418632     DOI: 10.1159/000112380

Source DB:  PubMed          Journal:  Dev Neurosci        ISSN: 0378-5866            Impact factor:   2.984


  11 in total

1.  Clonal analysis reveals granule cell behaviors and compartmentalization that determine the folded morphology of the cerebellum.

Authors:  Emilie Legué; Elyn Riedel; Alexandra L Joyner
Journal:  Development       Date:  2015-04-01       Impact factor: 6.868

2.  Descriptive epidemiology of cerebellar hypoplasia in the National Birth Defects Prevention Study.

Authors:  Meredith M Howley; Kim M Keppler-Noreuil; Christopher M Cunniff; Marilyn L Browne
Journal:  Birth Defects Res       Date:  2018-09-19       Impact factor: 2.344

3.  Preferential accumulation of [3H] corticosterone in chick brain during embryonic development.

Authors:  F Gremo; A Vernadakis
Journal:  Neurochem Res       Date:  1981-04       Impact factor: 3.996

4.  Glucocorticoid receptor stimulation and the regulation of neonatal cerebellar neural progenitor cell apoptosis.

Authors:  Kevin K Noguchi; Karen Lau; Derek J Smith; Brant S Swiney; Nuri B Farber
Journal:  Neurobiol Dis       Date:  2011-04-20       Impact factor: 5.996

5.  Effects of corticosterone on brain cholinergic enzymes in chick embryos.

Authors:  D Bau; A Vernadakis
Journal:  Neurochem Res       Date:  1982-07       Impact factor: 3.996

6.  Hedgehog signaling has a protective effect in glucocorticoid-induced mouse neonatal brain injury through an 11betaHSD2-dependent mechanism.

Authors:  Vivi M Heine; David H Rowitch
Journal:  J Clin Invest       Date:  2009-01-26       Impact factor: 14.808

7.  Glucocorticoid Induced Cerebellar Toxicity in the Developing Neonate: Implications for Glucocorticoid Therapy during Bronchopulmonary Dysplasia.

Authors:  Kevin K Noguchi
Journal:  Cells       Date:  2014-01-08       Impact factor: 6.600

8.  Association between postnatal dexamethasone for treatment of bronchopulmonary dysplasia and brain volumes at adolescence in infants born very preterm.

Authors:  Jeanie L Y Cheong; Alice C Burnett; Katherine J Lee; Gehan Roberts; Deanne K Thompson; Stephen J Wood; Alan Connelly; Peter J Anderson; Lex W Doyle
Journal:  J Pediatr       Date:  2013-12-12       Impact factor: 4.406

9.  Differential timing of granule cell production during cerebellum development underlies generation of the foliation pattern.

Authors:  Emilie Legué; Jackie L Gottshall; Edouard Jaumouillé; Alberto Roselló-Díez; Wei Shi; Luis Humberto Barraza; Senna Washington; Rachel L Grant; Alexandra L Joyner
Journal:  Neural Dev       Date:  2016-09-08       Impact factor: 3.842

Review 10.  Context modulates outcome of perinatal glucocorticoid action in the brain.

Authors:  E Ronald de Kloet; Sanne E F Claessens; Jiska Kentrop
Journal:  Front Endocrinol (Lausanne)       Date:  2014-07-09       Impact factor: 5.555

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