» Articles » PMID: 35278411

The Role of Lipid Second Messengers in Aldosterone Synthesis and Secretion

Overview
Journal J Lipid Res
Publisher Elsevier
Specialty Biochemistry
Date 2022 Mar 12
PMID 35278411
Authors
Affiliations
Soon will be listed here.
Abstract

Second messengers are small rapidly diffusing molecules or ions that relay signals between receptors and effector proteins to produce a physiological effect. Lipid messengers constitute one of the four major classes of second messengers. The hydrolysis of two main classes of lipids, glycerophospholipids and sphingolipids, generate parallel profiles of lipid second messengers: phosphatidic acid (PA), diacylglycerol (DAG), and lysophosphatidic acid versus ceramide, ceramide-1-phosphate, sphingosine, and sphingosine-1-phosphate, respectively. In this review, we examine the mechanisms by which these lipid second messengers modulate aldosterone production at multiple levels. Aldosterone is a mineralocorticoid hormone responsible for maintaining fluid volume, electrolyte balance, and blood pressure homeostasis. Primary aldosteronism is a frequent endocrine cause of secondary hypertension. A thorough understanding of the signaling events regulating aldosterone biosynthesis may lead to the identification of novel therapeutic targets. The cumulative evidence in this literature emphasizes the critical roles of PA, DAG, and sphingolipid metabolites in aldosterone synthesis and secretion. However, it also highlights the gaps in our knowledge, such as the preference for phospholipase D-generated PA or DAG, as well as the need for further investigation to elucidate the precise mechanisms by which these lipid second messengers regulate optimal aldosterone production.

Citing Articles

Multi-Omic Analysis of the Differences in Growth and Metabolic Mechanisms Between Chinese Domestic Cattle and Simmental Crossbred Cattle.

Wang J, Ni J, Jia X, Sun W, Lai S Int J Mol Sci. 2025; 26(4).

PMID: 40004011 PMC: 11855754. DOI: 10.3390/ijms26041547.


Oxidative Stress and Reprogramming of Lipid Metabolism in Cancers.

Li S, Yuan H, Li L, Li Q, Lin P, Li K Antioxidants (Basel). 2025; 14(2).

PMID: 40002387 PMC: 11851681. DOI: 10.3390/antiox14020201.


Metabolic phenotypes and fatty acid profiles associated with histopathology of primary aldosteronism.

Yang Y, Liu Y, Williams T, Gao M, Yan Y, Bao M Hypertens Res. 2025; .

PMID: 39939827 DOI: 10.1038/s41440-025-02143-w.


Sphingolipids and Chronic Kidney Disease.

Sakic Z, Atic A, Potocki S, Basic-Jukic N J Clin Med. 2024; 13(17).

PMID: 39274263 PMC: 11396415. DOI: 10.3390/jcm13175050.


Nephrectomy and high-salt diet inducing pulmonary hypertension and kidney damage by increasing Ang II concentration in rats.

Jiang Q, Yang Q, Zhang C, Hou C, Hong W, Du M Respir Res. 2024; 25(1):288.

PMID: 39080603 PMC: 11290206. DOI: 10.1186/s12931-024-02916-w.


References
1.
Isales C, Bollag W, Kiernan L, Barrett P . Effect of ANP on sustained aldosterone secretion stimulated by angiotensin II. Am J Physiol. 1989; 256(1 Pt 1):C89-95. DOI: 10.1152/ajpcell.1989.256.1.C89. View

2.
Kawarazaki W, Fujita T . The Role of Aldosterone in Obesity-Related Hypertension. Am J Hypertens. 2016; 29(4):415-23. PMC: 4886496. DOI: 10.1093/ajh/hpw003. View

3.
Rainey W, Saner K, Schimmer B . Adrenocortical cell lines. Mol Cell Endocrinol. 2004; 228(1-2):23-38. DOI: 10.1016/j.mce.2003.12.020. View

4.
Ozbay T, Merrill Jr A, Sewer M . ACTH regulates steroidogenic gene expression and cortisol biosynthesis in the human adrenal cortex via sphingolipid metabolism. Endocr Res. 2005; 30(4):787-94. DOI: 10.1081/erc-200044040. View

5.
Mele P, Duarte A, Paz C, Capponi A, Podesta E . Role of intramitochondrial arachidonic acid and acyl-CoA synthetase 4 in angiotensin II-regulated aldosterone synthesis in NCI-H295R adrenocortical cell line. Endocrinology. 2012; 153(7):3284-94. DOI: 10.1210/en.2011-2108. View