Skip to Content
Merck
  • Combination of direct infusion mass spectrometry and gas chromatography mass spectrometry for toxicometabolomic study of red blood cells and serum of mice Mus musculus after mercury exposure.

Combination of direct infusion mass spectrometry and gas chromatography mass spectrometry for toxicometabolomic study of red blood cells and serum of mice Mus musculus after mercury exposure.

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (2015-02-11)
M A García-Sevillano, T García-Barrera, F Navarro, N Abril, C Pueyo, J López-Barea, J L Gómez-Ariza
ABSTRACT

Although mercury (Hg) is an important environmental and occupational pollutant, its toxicological effects, especially in serum and red blood cells (RBCs), have been scarcely studied. A toxicometabolomics workflow based on high resolution mass spectrometry approaches has been applied to investigate the toxicological effects of Hg in Mus musculus mice after subcutaneous injection for 10 days, which produced inflammation and vacuolization, steatosis and karyolysis in the hepatic tissue. To this end, direct infusion mass spectrometry (DIMS) of polar and lipophilic extracts from serum and RBCs, using positive and negative mode of acquisition (ESI+/ESI-), and gas chromatography-mass spectrometry were used. A quantitative analysis of reversible oxidized thiols in serum proteins demonstrated a strong oxidative stress induction in the liver of Hg-exposed mice. Endogenous metabolites alterations were identified by partial least squares-discriminant analysis (PLS-DA). Mercury-exposed mice show perturbations in energy metabolism, amino acid metabolism, membrane phospholipid breakdown and oxidative stress-related metabolites in serum along the exposure. This work reports for the first time the effects of Hg-exposure on RBCs metabolic pathways, and reveals disturbances in glycolysis, membrane turnover, glutathione and ascorbate metabolisms.

MATERIALS
Product Number
Brand
Product Description

USP
Urea, United States Pharmacopeia (USP) Reference Standard
Sigma-Aldrich
Ethyl alcohol, Pure, 190 proof, ACS reagent, meets USP testing specifications, Excise Tax-free, Permit for use required
Sigma-Aldrich
Ethyl alcohol, Pure, 140 proof, Excise Tax-free, Permit for use required
Sigma-Aldrich
Pyridine, AR, ≥99.5%
Sigma-Aldrich
Pyridine, LR, ≥99%
Sigma-Aldrich
Ethyl alcohol, Pure, 140 proof, meets water USP testing specifications, Excise Tax-free, Permit for use required
Sigma-Aldrich
Acetic anhydride
Sigma-Aldrich
Formic acid, LR, ≥98%
Sigma-Aldrich
Formic acid, AR, ≥90%
Sigma-Aldrich
Urea, LR, ≥99%
Sigma-Aldrich
Formic acid, AR, ≥98%
Sigma-Aldrich
Formic acid, LR, ≥85%
Sigma-Aldrich
Nitric acid, LR, 69-72%
Urea, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
Urea, AR, ≥99%
Sigma-Aldrich
Ethylenediaminetetraacetic acid solution, 0.02 N
Sigma-Aldrich
Nitric acid, AR, 69-72%
Supelco
Pyridine, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
Ethylenediaminetetraacetic acid, Vetec, reagent grade, 98%
Supelco
Urea, analytical standard
USP
Methyl alcohol, United States Pharmacopeia (USP) Reference Standard
Sigma-Aldrich
Urea, Vetec, reagent grade, 99%
Sigma-Aldrich
Pyridine, suitable for HPLC, ≥99.9%
Sigma-Aldrich
Ethanol, purum, fine spirit, denaturated with 2% 2-butanone, F25 MEK1, ~96% (based on denaturant-free substance)
Sigma-Aldrich
Formic acid, ACS reagent, ≥96%
Sigma-Aldrich
Ethyl alcohol, Pure 200 proof, Molecular Biology
Sigma-Aldrich
Nitric acid, puriss. p.a., reag. ISO, reag. Ph. Eur., ≥65%
Sigma-Aldrich
Formic acid, puriss., meets analytical specifications of DAC, FCC, 98.0-100%
Sigma-Aldrich
Pyridine, ReagentPlus®, ≥99%
Sigma-Aldrich
Nitric acid, puriss. p.a., ≥65% (T)