The effect of in vivo hydrocortisone administration on the labelling index and size of the intra- and extra-adrenal chromaffin tissue of the fetal and perinatal mouse
- PMID: 4077704
- PMCID: PMC1165092
The effect of in vivo hydrocortisone administration on the labelling index and size of the intra- and extra-adrenal chromaffin tissue of the fetal and perinatal mouse
Abstract
Administration of hydrocortisone in vivo to pregnant mice between the eighth and sixteenth days of gestation leads to highly significant increases in both the volume and the labelling index of extra-adrenal chromaffin tissue (as represented by the para-aortic body) of 16 days fetal mice. The labelling index of intra-adrenal chromaffin cells increases slightly after hydrocortisone administration, but the volume of the adrenal chromaffin tissue was not assessed since the groups of chromaffin cells had not in all cases aggregated to form a distinct medulla. Hydrocortisone administration to mice for the last week of gestation also leads to a highly significant increase in the size and the labelling index of the perinatal para-aortic body. Although an increase in the labelling index of perinatal intra-adrenal chromaffin cells is brought about, this is much less marked than that of the extra-adrenal tissue and neither is it reflected by any increase in the volume of the now discernible adrenal medulla. These increases in size and labelling index of the para-aortic body constitute a hyperplastic response rather than a hypertrophic response. Various possible mechanisms and implications are discussed in the light of the development of chromaffin tissue and the effects of the cortex and its secretions on the medulla. Associated effects of hydrocortisone noted in this work are the resultant marked diminution of adrenocortical volume in the perinatal gland, and a slight fall in the labelling index of perinatal intra-adrenal haemopoietic cells.
Similar articles
-
A fraction of labelled mitoses study on adrenal chromaffin tissue in the newborn mouse and the effect of hydrocortisone.J Anat. 1988 Apr;157:105-9. J Anat. 1988. PMID: 3198471 Free PMC article.
-
The effect of hydrocortisone on the para-aortic body of the newborn mouse: an in vivo fraction of labelled mitoses study.J Anat. 1987 Feb;150:211-8. J Anat. 1987. PMID: 3654334 Free PMC article.
-
The effect of in vivo hydrocortisone administration on the labelling index and size of chromaffin tissue in the postnatal and adult mouse.J Anat. 1986 Feb;144:133-44. J Anat. 1986. PMID: 3693040 Free PMC article.
-
Fetal catecholamines.Am J Obstet Gynecol. 1983 Aug 1;146(7):840-55. doi: 10.1016/0002-9378(83)91088-8. Am J Obstet Gynecol. 1983. PMID: 6346884 Review.
-
The natural history of the chromaffin cell--twenty-five years on the beginning.Arch Histol Cytol. 1989;52 Suppl:331-41. doi: 10.1679/aohc.52.suppl_331. Arch Histol Cytol. 1989. PMID: 2510790 Review.
Cited by
-
A fraction of labelled mitoses study on adrenal chromaffin tissue in the newborn mouse and the effect of hydrocortisone.J Anat. 1988 Apr;157:105-9. J Anat. 1988. PMID: 3198471 Free PMC article.
-
The effect of hydrocortisone on the para-aortic body of the newborn mouse: an in vivo fraction of labelled mitoses study.J Anat. 1987 Feb;150:211-8. J Anat. 1987. PMID: 3654334 Free PMC article.
-
Effect of betamethasone on the expression of dopamine D1 receptor mRNA in the developing rabbit adrenal gland.Curr Ther Res Clin Exp. 2003 Sep;64(8):568-79. doi: 10.1016/j.curtheres.2003.09.009. Curr Ther Res Clin Exp. 2003. PMID: 24944405 Free PMC article.
-
Cell loss and autophagy in the extra-adrenal chromaffin organ of Zuckerkandl are regulated by glucocorticoid signalling.J Neuroendocrinol. 2013 Jan;25(1):34-47. doi: 10.1111/j.1365-2826.2012.02367.x. J Neuroendocrinol. 2013. PMID: 23078542 Free PMC article.
-
The effect of in vivo hydrocortisone administration on the labelling index and size of chromaffin tissue in the postnatal and adult mouse.J Anat. 1986 Feb;144:133-44. J Anat. 1986. PMID: 3693040 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources