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Tissue-specific corticosteroidogenesis in the rat.
A E Rudolph1, E R Blasi, J A Delyani
1Cardiovascular Discovery, Monsanto/Searle, St. Louis, MO 63167, USA.
Molecular and Cellular Endocrinology
|August 15, 2000
Summary
This study investigated local aldosterone production in rat tissues. Aldosterone synthesis enzymes were found in cardiac tissue, varying by rat strain and stimulation, potentially resolving scientific controversy.
Area of Science:
- Endocrinology
- Cardiovascular Physiology
- Molecular Biology
Background:
- Aldosterone is crucial for sodium balance and cardiovascular health.
- The existence of non-adrenal aldosterone biosynthesis, particularly in cardiac tissue, is debated.
- Understanding local steroidogenesis is key to resolving this controversy.
Purpose of the Study:
- To comprehensively evaluate steroid hormone biosynthetic capabilities in multiple rat tissues.
- To investigate the presence and regulation of aldosterone synthesis enzymes (P45011beta and P450aldo) in cardiac and other tissues.
- To compare these capabilities between Wistar and Sprague-Dawley rat strains under basal and stimulated conditions.
Main Methods:
- Utilized reverse transcriptase-polymerase chain reaction (RT-PCR) to detect gene expression.
- Examined tissue panels from Wistar and Sprague-Dawley rats.
- Assessed enzyme expression under unstimulated and Angiotensin II-stimulated conditions.
Main Results:
- Cardiac P45011beta and P450aldo were detected in Wistar rats but not Sprague-Dawley rats under unstimulated conditions.
- Angiotensin II stimulation upregulated myocardial expression of both enzymes in both rat strains.
- Angiotensin II reduced message levels of these enzymes in cerebral cortex and mesenteric arteries of both strains.
Conclusions:
- Demonstrates the potential for local steroid synthesis in vascular, cardiac, renal, and neuronal tissues.
- Reveals differential regulation of non-adrenal aldosterone biosynthesis between rat strains.
- Suggests this variability may resolve the controversy surrounding non-adrenal steroidogenic systems.