YAMASHITA Kaoru
   Department   School of Medicine(Tokyo Women's Medical University Hospital), School of Medicine
   Position  
Article types Original article
Language English
Peer review Peer reviewed
Title Adrenal cortex hypoxia modulates aldosterone production in heart failure.
Journal Formal name:Biochemical and biophysical research communications
Abbreviation:Biochem Biophys Res Commun
ISSN code:10902104/0006291X
Volume, Issue, Page 524(1),pp.184-189
Author and coauthor YAMASHITA Kaoru†, ITO Kentaro, ENDO Jin**, MATSUHASHI Tomohiro, KATSUMATA Yoshinori, YAMAMOTO Tsunehisa, SHIRAKAWA Kohsuke, ISOBE Sarasa, KATAOKA Masaharu, YOSHIDA Naohiro, GOTO Shinichi, MORIYAMA Hidenori, KITAKATA Hiroki, MITANI Fumiko, FUKUDA Keiichi, GODA Nobuhito, ICHIHARA Atsuhiro, SANO Motoaki*
Authorship Lead author
Publication date 2020/03
Summary Plasma aldosterone concentration increases in proportion to the severity of heart failure, even during treatment with renin-angiotensin system inhibitors. This study investigated alternative regulatory mechanisms of aldosterone production that are significant in heart failure. Dahl salt-sensitive rats on a high-salt diet, a rat model of heart failure with cardio-renal syndrome, had high plasma aldosterone levels and elevated β3-adrenergic receptor expression in hypoxic zona glomerulosa cells. In H295R cells (a human adrenocortical cell line), hypoxia-induced β3-adrenergic receptor expression. Hypoxia-mediated β3-adrenergic receptor expression augmented aldosterone production by facilitating hydrolysis of lipid droplets though ERK-mediated phosphorylation of hormone-sensitive lipase, also known as cholesteryl ester hydrolase. Hypoxia also accelerated the synthesis of cholesterol esters by acyl-CoA:cholesterol acyltransferase, thereby increasing the cholesterol ester content in lipid droplets. Thus, hypoxia enhanced aldosterone production by zona glomerulosa cells via promotion of the accumulation and hydrolysis of cholesterol ester in lipid droplets. In conclusion, hypoxic zona glomerulosa cells with heart failure show enhanced aldosterone production via increased catecholamine responsiveness and activation of cholesterol trafficking, irrespective of the renin-angiotensin system.
DOI 10.1016/j.bbrc.2020.01.088
PMID 31982132