Regulation of aldosterone synthesis and secretion.
Abstract
Aldosterone is a steroid hormone synthesized in and secreted from the outer layer of the adrenal cortex, the zona glomerulosa. Aldosterone is responsible for regulating sodium homeostasis, thereby helping to control blood volume and blood pressure. Insufficient aldosterone secretion can lead to hypotension and circulatory shock, particularly in infancy. On the other hand, excessive aldosterone levels, or those too high for sodium status, can cause hypertension and exacerbate the effects of high blood pressure on multiple organs, contributing to renal disease, stroke, visual loss, and congestive heart failure. Aldosterone is also thought to directly induce end-organ damage, including in the kidneys and heart. Because of the significance of aldosterone to the physiology and pathophysiology of the cardiovascular system, it is important to understand the regulation of its biosynthesis and secretion from the adrenal cortex. Herein, the mechanisms regulating aldosterone production in zona glomerulosa cells are discussed, with a particular emphasis on signaling pathways involved in the secretory response to the main controllers of aldosterone production, the renin-angiotensin II system, serum potassium levels and adrenocorticotrophic hormone. The signaling pathways involved include phospholipase C-mediated phosphoinositide hydrolysis, inositol 1,4,5-trisphosphate, cytosolic calcium levels, calcium influx pathways, calcium/calmodulin-dependent protein kinases, diacylglycerol, protein kinases C and D, 12-hydroxyeicostetraenoic acid, phospholipase D, mitogen-activated protein kinase pathways, tyrosine kinases, adenylate cyclase, and cAMP-dependent protein kinase. A complete understanding of the signaling events regulating aldosterone biosynthesis may allow the identification of novel targets for therapeutic interventions in hypertension, primary aldosteronism, congestive heart failure, renal disease, and other cardiovascular disorders.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
A low-sodium diet does not directly affect aldosterone secretion, but indirectly through activation of the RAAS, upregulation of AT1 receptor levels, and hyperplasia of the zona glomerulosa.
“A low-sodium diet does not directly affect the aldosterone secretion, but indirectly through activation of the RAAS, upregulation of AT1 receptor levels, and hyperplasia of the zona glomerulosa (Bollag, 2014).”
From Thoroughly Calibrated Modular Agent-Based Model of the Human Cardiovascular and Renal Systems for Blood Pressure Regulation in Health and Disease (2021) · cites this paper as Bollag, 2014
A rise of 1 mmol/l in serum potassium concentration doubles the aldosterone secretion.
“A rise of 1 mmol/l in serum potassium concentration doubles the aldosterone secretion (Pralong et al., 1992; Bollag, 2014).”
From Thoroughly Calibrated Modular Agent-Based Model of the Human Cardiovascular and Renal Systems for Blood Pressure Regulation in Health and Disease (2021) · cites this paper as Bollag, 2014
The citation lists haven’t been fetched yet
References 348 · Cited by 180
- Authors
- Bollag, W. B.
- Affiliations
- Augusta University (US)
- Corresponding author
- Bollag, Wendy B.
- ORCID
- Bollag, Wendy B.
- Venue
- Comprehensive Physiology
- Publisher
- Wiley
- Published
- 2014-08-07
- Volume
- 4
- Issue
- 3
- Pages
- 1017-1055
- ISSN
- 2040-4603 (ISSN-L)
- OpenAlex
- W2140016629
- Cited by
- 180
- References
- 348
- Citations by year
- 2026: 4 · 2025: 12 · 2024: 24 · 2023: 21 · 2022: 10 · 2021: 16 · 2020: 16 · 2019: 22 · 2018: 15 · 2017: 13 · 2016: 21 · 2015: 4 · 2014: 2
- Type
- other
- Language
- en
- Open access
- closed
- Locations
- Comprehensive physiology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal Regulation and Hypertension
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Renin-Angiotensin System Studies
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Keywords
- aldosterone biosynthesis, aldosterone secretion, zona glomerulosa, adrenal cortex, serum potassium, ACTH, signaling pathways, phospholipase C, inositol 1,4,5-trisphosphate, calcium signaling, calcium/calmodulin-dependent protein kinase, diacylglycerol, protein kinase C, phospholipase D, mitogen-activated protein kinase, adenylate cyclase, protein kinase A, hypertension, primary aldosteronism, congestive heart failure, kidney disease, sodium homeostasis
- MeSH terms
- Adrenocorticotropic Hormone, Aldosterone, Angiotensin II, Animals, Humans, Potassium, Zona Glomerulosa, Receptors, G-Protein-Coupled, Receptor, Angiotensin, Type 1
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review