Accéder au contenu
Merck

Oxidative stress in patients with multiple sclerosis.

Ukrains'kyi biokhimichnyi zhurnal (1999 ) (1999-12-28)
C Syburra, S Passi
RÉSUMÉ

It is well known that brain and nervous system cells are prone to oxidative damage because of their relatively low content of antioxidants, especially enzymatic ones, and of the high levels of both membrane polyunsaturated fatty acids (PUFA) and iron easily released from injured cells. We have investigated the oxidative stress in the blood (plasma, erythrocytes and lymphocytes) of 28 patients affected with multiple sclerosis (MS) and of 30 healthy age matched controls, by performing a multiparameter analysis of non-enzymatic and enzymatic antioxidants--Vitamin E (Vit. E), ubiquinone (UBI), reduced and oxidized glutathione (GSH, GS-SG), superoxide dismutase (SOD), glutathione peroxidase (GPX), catalase (CAT) and fatty acid patterns of phospholipids (PL-FA). PL-FA and Vit. E were assayed by GC-MS; UBI and GSH/GS-SG by HPLC; SOD, GPX and CAT by spectrophotometry. In comparison to controls, patients with MS showed significantly reduced levels of plasma UBI (0.21 +/- 0.10 vs. 0.78 +/- 0.08 mg/ml, p < 0.001), plasma Vit. E (7.4 +/- 2.1 vs. 11.4 +/- 1.8 mg/ml, p < 0.01), lymphocyte UBI (8.1 +/- 4.0 vs. 30.3 +/- 7.2 ng/ml blood, p < 0.001) and erythrocyte GPX (22.6 +/- 5.7 vs. 36.3 +/- 6.4 U/g Hb, p < 0.001). This blood antioxidant deficiency was associated with plasma levels of PL-PUFA--especially C20:3 n-6 and C20:4 n-6--significantly higher than controls. In conclusion, the blood of patients with MS shows the signs of a significant oxidative stress. The possibility of counteracting it by antioxidant administration plus an appropriate diet, might represent a promising way of inhibiting the progression of the disease. Antioxidant supplements should include not only GSH repleting agents, but also Vit. E, ubiquinol, and selenium.

MATÉRIAUX
Référence du produit
Marque
Description du produit

Sigma-Aldrich
Acide acétique, glacial, ACS reagent, ≥99.7%
Sigma-Aldrich
Acide acétique, glacial, ReagentPlus®, ≥99%
Sigma-Aldrich
Acide acétique, glacial, ≥99.99% trace metals basis
Sigma-Aldrich
Acide acétique solution, suitable for HPLC
Sigma-Aldrich
Acide acétique, glacial, puriss., meets analytical specification of Ph. Eur., BP, USP, FCC, 99.8-100.5%
Sigma-Aldrich
L-cystéine, 97%
Sigma-Aldrich
L-Glutathion oxydé, ≥98% (HPLC)
Sigma-Aldrich
L-cystéine, from non-animal source, BioReagent, suitable for cell culture, ≥98%
Sigma-Aldrich
Acide acétique, glacial, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥99.8%
Sigma-Aldrich
L-Glutathion réduit, suitable for cell culture, BioReagent, ≥98.0%, powder
Sigma-Aldrich
Zinc, dust, <10 μm, ≥98%
Sigma-Aldrich
Aluminum, powder, ≥91% (complexometric)
Sigma-Aldrich
Magnésium, powder, ≥99%
Sigma-Aldrich
Zinc, powder, <150 μm, 99.995% trace metals basis
Sigma-Aldrich
L-cystéine, BioUltra, ≥98.5% (RT)
Sigma-Aldrich
Acide acétique, for luminescence, BioUltra, ≥99.5% (GC)
Sigma-Aldrich
L-Glutathion réduit, ≥98.0%
Sigma-Aldrich
Copper, powder, 99.999% trace metals basis
Sigma-Aldrich
Tin, ≥99%, powder
Sigma-Aldrich
Silicon, powder, −325 mesh, 99% trace metals basis
Sigma-Aldrich
Copper, foil, thickness 0.25 mm, 99.98% trace metals basis
Sigma-Aldrich
Nickel de Raney®, W.R. Grace and Co. Raney® 2800, slurry, in H2O, active catalyst
Sigma-Aldrich
Copper, powder, <425 μm, 99.5% trace metals basis
SAFC
L-cystéine
Sigma-Aldrich
Acide acétique, ≥99.5%, FCC, FG
Sigma-Aldrich
Calcium, granular, 99%
Sigma-Aldrich
Manganese, powder, ≥99.9% trace metals basis
Sigma-Aldrich
Acide acétique, natural, ≥99.5%, FG
Sigma-Aldrich
Copper, wire, diam. 1.0 mm, ≥99.9%
Sigma-Aldrich
Tin, powder, <150 μm, 99.5% trace metals basis