The effects of estradiol benzoate (EB) on steroidogenesis in rat zona fasciculata-reticularis (ZFR) cells were studied. Female rats were ovariectomized (Ovx) for 2 weeks and then injected subcutaneously with oil or EB for 3 days before decapitation. ZFR cells were isolated and incubated with adrenoc
Effects of estradiol on aldosterone secretion in ovariectomized rats
โ Scribed by Mei-Mei Kau; Ming-Jae Lo; Shiow-Chwen Tsai; Jiann-Jong Chen; Chien-Chen Lu; Ho Lin; Shyi-Wu Wang; Paulus S. Wang
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 114 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0730-2312
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โฆ Synopsis
The effects and action mechanisms of estradiol on aldosterone secretion in female rats were studied. Replacement of estradiol benzoate (EB) increased the levels of plasma estradiol and aldosterone in ovariectomized (Ovx) rats. The aldosterone release from zona glomerulosa (ZG) cells was higher in EB-treated rats than in oil-treated animals. EB treatment potentiated the responses of aldosterone release to adrenocorticotropic hormone (ACTH), forskolin (FSK), and 8-bromoadenosine 3ะ, 5ะ-cyclic monophosphate (8-Br-cAMP). Administration of EB in vivo did not alter cAMP production in response to ACTH or FSK. Although angiotensin II (Ang II) increased aldosterone secretion by rat ZG cells, the stimulatory effect of Ang II on the release of aldosterone was not altered by EB treatment. The conversions of [ 3 H]-deoxycorticosterone to [ 3 H]-corticosterone and [ 3 H]-corticosterone to [ 3 H]-aldosterone in EB-treated groups were greater than those in the oil-treated group. These results suggest that estradiol increases aldosterone secretion in part through the mechanisms involving the activation of the post-cAMP pathway, 11โค-hydroxylase and aldosterone synthase activity.
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Acute effects and action mechanisms of prolactin (PRL) on aldosterone secretion in zona glomerulosa (ZG) cells were investigated in ovariectomized rats. Administration of ovine PRL (oPRL) increased aldosterone secretion in a dose-dependent manner. Incubation of [3H]-pregnenolone combined with oPRL i