Identification of putative natriuretic hormones isolated from human urine.

This brief review describes some representative methodological approaches to the isolation of putative endogenous inhibitors of epithelial sodium transport - i. e. as ouabain-like factors (OLF) that inhibit the sodium transport enzyme Na-K-ATPase or inhibit the epithelial sodium channel (ENaC). Gel...

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Main Author: Herbert J Kramer
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-05-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fendo.2015.00066/full
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spelling doaj-caded15b20d9468ea59c3cafb6b597b72020-11-24T20:46:41ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922015-05-01610.3389/fendo.2015.00066134609Identification of putative natriuretic hormones isolated from human urine.Herbert J Kramer0Rheinische-Friedrich-Wilhelms-UniversityThis brief review describes some representative methodological approaches to the isolation of putative endogenous inhibitors of epithelial sodium transport - i. e. as ouabain-like factors (OLF) that inhibit the sodium transport enzyme Na-K-ATPase or inhibit the epithelial sodium channel (ENaC). Gel chromatography and reverse-phase (RP)-HPLC of lyophilized and reconstituted 24h-urine from salt-loaded healthy humans led to two active fractions, a hydrophilic OLF-1 and a lipophilic OLF-2 whose mass (Ms)-spectroscopic data indicate a Mr of 391 (1,2). Further identification was attempted by Ms-, IR-, UV- and 1H-NMR- spectroscopy. OLF-1 and OLF-2 may be closely related if not identical to (di)ascorbic acid or its salts such as vanadium (V)-Vv-diascorbate with Mr 403 (3) and VIV-diascorbate. OLF-1 and Vv-diascorbate are about 10-fold stronger inhibitors of Na-K-ATPase than OLF-2 and VIV-diascorbate, respectively. In conscious rats, i.v. infusion of OLF-1 and OLF-2 resulted in a strong natriuresis. In a similar study Cain et al. (4) isolated a sodium transport inhibitor from the urine of uremic patients by gel chromatography and RP-HPLC. In uremic rats a natriuretic response to the injection of the active material was found. Xanthurenic acid 8-O-ß-D-glucoside (Mr 368) and xanthurenic acid 8-O-sulfate (Mr 284) were identified as endogenous inhibitors of sodium transport acting, e.g. by ENaC blockade. No definite relation to blood pressure, body fluid volume or sodium balance has been reported for any of these above factors and further studies to identify the natriuretic and/or ouabain-like compound(s) or hormone(s) will be needed.http://journal.frontiersin.org/Journal/10.3389/fendo.2015.00066/fullsodium transportnatriuretic hormoneendogenous inhibitorsHuman urineepithelial sodium transport
collection DOAJ
language English
format Article
sources DOAJ
author Herbert J Kramer
spellingShingle Herbert J Kramer
Identification of putative natriuretic hormones isolated from human urine.
Frontiers in Endocrinology
sodium transport
natriuretic hormone
endogenous inhibitors
Human urine
epithelial sodium transport
author_facet Herbert J Kramer
author_sort Herbert J Kramer
title Identification of putative natriuretic hormones isolated from human urine.
title_short Identification of putative natriuretic hormones isolated from human urine.
title_full Identification of putative natriuretic hormones isolated from human urine.
title_fullStr Identification of putative natriuretic hormones isolated from human urine.
title_full_unstemmed Identification of putative natriuretic hormones isolated from human urine.
title_sort identification of putative natriuretic hormones isolated from human urine.
publisher Frontiers Media S.A.
series Frontiers in Endocrinology
issn 1664-2392
publishDate 2015-05-01
description This brief review describes some representative methodological approaches to the isolation of putative endogenous inhibitors of epithelial sodium transport - i. e. as ouabain-like factors (OLF) that inhibit the sodium transport enzyme Na-K-ATPase or inhibit the epithelial sodium channel (ENaC). Gel chromatography and reverse-phase (RP)-HPLC of lyophilized and reconstituted 24h-urine from salt-loaded healthy humans led to two active fractions, a hydrophilic OLF-1 and a lipophilic OLF-2 whose mass (Ms)-spectroscopic data indicate a Mr of 391 (1,2). Further identification was attempted by Ms-, IR-, UV- and 1H-NMR- spectroscopy. OLF-1 and OLF-2 may be closely related if not identical to (di)ascorbic acid or its salts such as vanadium (V)-Vv-diascorbate with Mr 403 (3) and VIV-diascorbate. OLF-1 and Vv-diascorbate are about 10-fold stronger inhibitors of Na-K-ATPase than OLF-2 and VIV-diascorbate, respectively. In conscious rats, i.v. infusion of OLF-1 and OLF-2 resulted in a strong natriuresis. In a similar study Cain et al. (4) isolated a sodium transport inhibitor from the urine of uremic patients by gel chromatography and RP-HPLC. In uremic rats a natriuretic response to the injection of the active material was found. Xanthurenic acid 8-O-ß-D-glucoside (Mr 368) and xanthurenic acid 8-O-sulfate (Mr 284) were identified as endogenous inhibitors of sodium transport acting, e.g. by ENaC blockade. No definite relation to blood pressure, body fluid volume or sodium balance has been reported for any of these above factors and further studies to identify the natriuretic and/or ouabain-like compound(s) or hormone(s) will be needed.
topic sodium transport
natriuretic hormone
endogenous inhibitors
Human urine
epithelial sodium transport
url http://journal.frontiersin.org/Journal/10.3389/fendo.2015.00066/full
work_keys_str_mv AT herbertjkramer identificationofputativenatriuretichormonesisolatedfromhumanurine
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