ANGIOTENSIN-II RECEPTOR SUBTYPES IN THE ADRENALS OF PREGNANT RATS

Citation
I. Forcier et al., ANGIOTENSIN-II RECEPTOR SUBTYPES IN THE ADRENALS OF PREGNANT RATS, Molecular and cellular endocrinology, 114(1-2), 1995, pp. 177-186
Citations number
45
Categorie Soggetti
Endocrynology & Metabolism","Cell Biology
ISSN journal
03037207
Volume
114
Issue
1-2
Year of publication
1995
Pages
177 - 186
Database
ISI
SICI code
0303-7207(1995)114:1-2<177:ARSITA>2.0.ZU;2-A
Abstract
During human and rat pregnancy, several hemodynamic and endocrine proc esses are markedly modified. These include activation of the renin-ang iotensin system (RAS) and increase of plasma aldosterone. However, the rise of plasma aldosterone is greater than expected from the elevatio n of RAS activity. Gestational alterations in angiotensin II receptors (AT receptor) in the adrenal could explain this apparent hyperaldoste ronism. This study was conducted to determine differences between AT r eceptor subtypes in the adrenal glands of non-pregnant and pregnant (2 2 days) rats. Using plasma membrane preparations from adrenal glomerul osa and medulla, we determined receptor density and affinity with I-12 5-angiotensin II(ANG II); the AT receptor subtypes were assessed by di splacement of I-125-ANG II binding with subtype-specific antagonists ( DuP753 and PD123319). In zona glomerulosa of non-pregnant and pregnant rats, AT(1) receptors predominated(approximate to 80%) with no statis tical difference in receptor density (B-max) and affinity (K-d) and th e ratio of receptor subtypes between the two groups of rats. In adrena l medulla of both groups of rats, the major portion of I-125-ANG II bi nding (60-70%) was displaced by the AT(1) receptor antagonist, PD12331 9. Neither B-max nor K-d differed in this tissue during gestation. The results for AT(1) receptor density were confirmed by Western blot. No rthern blot analysis showed that AT(1) mRNA level in the adrenal is no t modified by gestation. These results indicate that the number, the a ffinity and the transcription of the AT(1) receptor in the adrenal are not altered during pregnancy, indicating that the rise in aldosterone secretion during pregnancy could not be explained by increase of AT(1 ) receptors in the zona glomerulosa, or modification of AT(1)/AT(2) ra tio.