Direkt zum Inhalt
Merck
  • Accumulation of trimethylamine and trimethylamine-N-oxide in end-stage renal disease patients undergoing haemodialysis.

Accumulation of trimethylamine and trimethylamine-N-oxide in end-stage renal disease patients undergoing haemodialysis.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association (2006-01-13)
Marcus A Bain, Randall Faull, Gianfranco Fornasini, Robert W Milne, Allan M Evans
ZUSAMMENFASSUNG

Trimethylamine (TMA) is a short-chain tertiary aliphatic amine that is derived from the diet either directly from the consumption of foods high in TMA or by the intake of food high in precursors to TMA, such as trimethylamine-N-oxide (TMNO), choline and L-carnitine. The clinical significance of TMA may be related to its potential to contribute to neurological toxicity and 'uraemic breath' in patients with end-stage renal disease (ESRD). Concentrations of TMA and TMNO in plasma from 10 healthy adults (not on haemodialysis) and 10 adults with ESRD undergoing haemodialysis (pre- and post-dialysis) were determined by gas chromatography-mass spectrometry. The concentrations of TMA and TMNO in pre-dialysis plasma (1.39+/-0.483 and 99.9+/-31.9 microM, respectively) were significantly (P<0.05) higher than the corresponding levels in healthy subjects (0.418+/-0.124 and 37.8+/-20.4 microM, respectively). However, there were no significant differences between post-dialysis and healthy subject plasma concentrations. In the ESRD patients, there was a significant (P<0.05) reduction in plasma TMA (from 1.39+/-0.483 to 0.484+/-0.164 microM) and TMNO (from 99.9+/-31.9 to 41.3+/-18.8 microM) during a single haemodialysis session. TMA and TMNO accumulate between haemodialysis sessions in ESRD patients, but are efficiently removed during a single haemodialysis session.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Ethyl alcohol, Pure 200 proof, Molecular Biology
Sigma-Aldrich
Aceton, ACS reagent, ≥99.5%
Sigma-Aldrich
Ethyl alcohol, Pure, 200 proof, ACS reagent, ≥99.5%
Sigma-Aldrich
Aceton, suitable for HPLC, ≥99.9%
Sigma-Aldrich
Aceton, HPLC Plus, for HPLC, GC, and residue analysis, ≥99.9%
Sigma-Aldrich
Ethyl alcohol, Pure, 200 proof, meets USP testing specifications
Sigma-Aldrich
Ethyl alcohol, Pure, 200 proof, anhydrous, ≥99.5%
Sigma-Aldrich
Ethyl alcohol, Pure 190 proof, for molecular biology
Sigma-Aldrich
Ethyl alcohol, Pure, 190 proof, ACS spectrophotometric grade, 95.0%
Sigma-Aldrich
Zink, dust, <10 μm, ≥98%
Sigma-Aldrich
Ethanol, BioUltra, Molecular Biology, ≥99.8%, (absolute alcohol, without additive, A15 o1)
Sigma-Aldrich
Aceton, ACS reagent, ≥99.5%
Sigma-Aldrich
Zink, granular, 20-30 mesh, ACS reagent, ≥99.8%
Supelco
Aceton, analytical standard
Sigma-Aldrich
Zink, powder, <150 μm, 99.995% trace metals basis
Sigma-Aldrich
Inosin, ≥99% (HPLC)
Sigma-Aldrich
Dimethylamin -Lösung, 40 wt. % in H2O
Supelco
Ethanol, wasserfrei, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
Trimethylamin-N-oxid, 95%
Supelco
Ethanol, standard for GC
Sigma-Aldrich
Ethanol, purum, fine spirit, denaturated with 4.8% methanol, F25 METHYL1, ~96% (based on denaturant-free substance)
Sigma-Aldrich
Cadaverin, 95%
Sigma-Aldrich
Dimethylamin -Lösung, 2.0 M in THF
Sigma-Aldrich
Phenylessigsäure, 99%
Sigma-Aldrich
Dimethylamin, anhydrous, ≥99%
Sigma-Aldrich
Aceton, histological grade, ≥99.5%
Sigma-Aldrich
Trimethylamin -Lösung, 43.0-49.0% in H2O (T)
Supelco
Aceton, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
Zink, foil, thickness 0.25 mm, 99.9% trace metals basis
Supelco
Ethanol-50, 50 mg/dL in H2O, ampule of 10 × 1.2 mL, certified reference material, Cerilliant®