Document Detail


The effect of hydrocortisone on the para-aortic body of the newborn mouse: an in vivo fraction of labelled mitoses study.
MedLine Citation:
PMID:  3654334     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Information about the cell cycle of the mouse para-aortic body within the first 24 hours of postnatal life was derived from a fraction of labelled mitoses study. The total cell cycle time was 8 1/2 hours, being made up as follows: S phase-2 hours; G2 phase-1 hour; M phase-3 1/2 hours (by analysis of the results, not by assumption) and G1 phase-2 hours (by subtraction). Problems are discussed regarding the length of G2 and M phases and the consequences for G1. After hydrocortisone administration (40 mg/kg/day) to female mice for the last seven days of pregnancy, the pattern in newborn mice was disrupted. Values for G2 and M were similar to those of the untreated group, but no values were obtainable for the other phases of the cell cycle or for the total cell cycle time. These results after hydrocortisone treatment could be explained by the superimposition of the cell cycles of two or more different groups of cells. They are discussed with regard to the life span of the para-aortic body, and their implications are considered in the light of previously reported glucocorticoid-induced transformations of small granule cells from cervical sympathetic ganglia into catecholamine-storing chromaffin cells. The established hyperplastic effect of hydrocortisone on the para-aortic body is therefore not the result simply of an acceleration of the cell cycle, but it may involve the incorporation into the proliferative compartment of cells previously either moribund or nonproliferating.
Authors:
W S Monkhouse; J Chell
Related Documents :
1414604 - Immunomodulation of c3h/hej cells by endotoxin associated protein and lipopolysaccharid...
7833384 - Existence of a commitment program for mitosis in early g1 in tumour cells.
7116934 - Cytogenetic and flow cytometric studies of cells from patients with fanconi's anemia.
15145774 - G0-g1 cell cycle phase transition as revealed by fluorescence resonance energy transfer...
25271834 - Chloroquine is a zinc ionophore.
7370984 - Thioguanine-induced s and g2 blocks and their significance to the mechanism of cytotoxi...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Journal of anatomy     Volume:  150     ISSN:  0021-8782     ISO Abbreviation:  J. Anat.     Publication Date:  1987 Feb 
Date Detail:
Created Date:  1987-11-16     Completed Date:  1987-11-16     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  0137162     Medline TA:  J Anat     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  211-8     Citation Subset:  IM    
Affiliation:
Department of Human Morphology, Nottingham University Medical School.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Animals, Newborn
Autoradiography
Cell Cycle / drug effects
Chromaffin System / drug effects*
Female
Hydrocortisone / pharmacology*
Maternal-Fetal Exchange
Mice
Mice, Inbred Strains
Mitosis
Para-Aortic Bodies / cytology,  drug effects*
Pregnancy
Chemical
Reg. No./Substance:
50-23-7/Hydrocortisone
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  A quantitative study of Australian aboriginal and Caucasian brains.
Next Document:  The embryonic origin of connective tissue mast cells.