Urinary prostasin in humans: relationships among prostasin, aldosterone and epithelial sodium channel activity View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2009-02-27

AUTHORS

Aya Koda, Naoki Wakida, Kazuhiro Toriyama, Kazutoshi Yamamoto, Hiromi Iijima, Kimio Tomita, Kenichiro Kitamura

ABSTRACT

Prostasin, a membrane-bound serine protease, is known to increase the activity of the epithelial sodium channel (ENaC). Gene expression of prostasin was shown to be regulated by aldosterone, which increases the rate of sodium reabsorption through ENaC. To clarify the physiological relationships among prostasin, aldosterone and ENaC, we developed a specific radioimmunoassay (RIA) for human prostasin. Prostasin levels in urine were determined in 26 normotensive and 121 hypertensive subjects. Aldosterone content in urine and plasma, urinary Na/K ratio and other clinical parameters were also measured. We observed a highly significant correlation between prostasin and aldosterone concentration in urine (correlation coefficient: 0.673, P<0.0001). A significant correlation was also found between urinary prostasin and plasma aldosterone concentration (correlation coefficient: 0.229, P<0.05). In addition, urinary prostasin excretion was inversely correlated with urinary Na/K ratio (correlation coefficient: −0.425, P<0.0001). In conclusion, we developed a prostasin-specific RIA and applied it to the clinical study. Our findings suggest that urinary prostasin level is strongly correlated with urinary or plasma aldosterone level and may serve as a surrogate marker for ENaC activation in hypertensive patients. However, it is not clear, at the present time, whether endogenous aldosterone regulates prostasin expression or vice versa. More... »

PAGES

276-281

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/hr.2009.6

DOI

http://dx.doi.org/10.1038/hr.2009.6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1050294652

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/19262497


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