Document Detail


Effect of adrenocorticotropin administration on the biosynthesis of corticosteroid-binding globulin in fetal sheep.
MedLine Citation:
PMID:  1848507     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Parturition in sheep is initiated by the fetus through activation of the fetal hypothalamic-pituitary-adrenal axis and is associated with increased concentrations of ACTH, cortisol, and corticosteroid-binding globulin (CBG) in the fetal circulation during the final 10-15 days of pregnancy. Premature parturition and a precocious elevation in fetal plasma CBG are produced by intrafetal ACTH administration, but the possible sources of CBG in the ovine fetus are not known. To determine these sites, CBG mRNA was measured in tissues from fetal sheep in late pregnancy and after intrafetal ACTH treatment, using a sheep CBG cDNA. Fetal ACTH treatment caused a significant increase in the fetal plasma corticosteroid-binding capacity (CBC), although there was no significant difference in CBC between umbilical arterial and umbilical venous plasma. After ACTH treatment, CBC was elevated in fetal liver and kidney. Cortisol binding in these tissues had characteristics similar to those of cortisol binding in fetal sheep plasma. By Northern blot analysis a single mRNA (1.7 kilobases) for CBG was detected in fetal liver, kidney, lung, and adrenal, but not in placenta. The abundance of CBG mRNA in the fetal liver was greater than that in other tissues, but was unchanged by ACTH treatment. The level of CBG mRNA in the fetal kidney, but not in other tissues, increased 3-fold after ACTH. We conclude that the elevation in plasma CBC after intrafetal ACTH, and presumably also at term pregnancy, does not reflect production of CBC by the placenta or transfer from the mother. Rather, it results from production primarily in the fetal liver and kidney, although only in the latter tissue is CBG mRNA accumulation increased by intrafetal ACTH treatment.
Authors:
R A Jacobs; V K Han; G L Hammond; J R Challis
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Endocrinology     Volume:  128     ISSN:  0013-7227     ISO Abbreviation:  Endocrinology     Publication Date:  1991 Apr 
Date Detail:
Created Date:  1991-04-23     Completed Date:  1991-04-23     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0375040     Medline TA:  Endocrinology     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  1960-6     Citation Subset:  AIM; IM    
Affiliation:
Lawson Research Institute, St. Joseph's Health Centre, London, Ontario, Canada.
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MeSH Terms
Descriptor/Qualifier:
Adrenal Glands / chemistry,  embryology
Adrenocorticotropic Hormone / pharmacology*
Animals
Female
Fetal Blood / metabolism
Fetus / drug effects,  metabolism*
Hydrocortisone / metabolism
Kidney / chemistry,  embryology,  metabolism
Liver / chemistry,  embryology,  metabolism
Lung / chemistry,  embryology
Nucleic Acid Hybridization
Pregnancy
RNA, Messenger / analysis,  metabolism
Sheep
Transcortin / biosynthesis*,  genetics
Umbilical Arteries
Umbilical Veins
Chemical
Reg. No./Substance:
0/RNA, Messenger; 50-23-7/Hydrocortisone; 9002-60-2/Adrenocorticotropic Hormone; 9010-38-2/Transcortin

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


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