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Determination of asymmetric dimethylarginine (ADMA) using a novel ELISA assay.

Authors :
Schulze F
Wesemann R
Schwedhelm E
Sydow K
Albsmeier J
Cooke JP
Böger RH
Source :
Clinical chemistry and laboratory medicine [Clin Chem Lab Med] 2004; Vol. 42 (12), pp. 1377-83.
Publication Year :
2004

Abstract

Asymmetric dimethylarginine (ADMA) is an endogenous competitive inhibitor of nitric oxide synthase (NOS). Elevated ADMA plasma levels have been reported in connection with diseases associated with an impaired endothelial L-arginine-NO pathway and endothelial dysfunction, such as atherosclerosis, hypercholesterolemia, chronic heart failure, diabetes mellitus, and hypertension. NO production by NOS is decreased due to elevated ADMA levels. In fact, there is increasing interest in determination of ADMA levels in samples of various origins. The aim of this work was to develop a precise and easy immunoassay in contrast to the existing methods, such as HPLC, liquid chromatography-mass spectrometry (LC-MS) and gas chromatography (GC)-MS. We determined cross-reactivity in our immunoassay of 1.2% for symmetric dimethylarginine and <0.02% for L-arginine. The limit of quantitation was 0.05 micromol/l. We found good correlation of the values measured when we compared our assay with LC-tandem MS (n = 29; r = 0.984; p < 0.0001). We determined ADMA levels in human serum and plasma, mouse and rat plasma, and cell culture supernatant. For human plasma we found a mean of 0.65 micromol/l in healthy subjects. In the plasma of mice and rats we found mean concentrations of 1.05 and 1.09 micromol/l, respectively.

Details

Language :
English
ISSN :
1434-6621
Volume :
42
Issue :
12
Database :
MEDLINE
Journal :
Clinical chemistry and laboratory medicine
Publication Type :
Academic Journal
Accession number :
15576299
Full Text :
https://doi.org/10.1515/CCLM.2004.257