Erythrocyte nitric oxide synthase as a surrogate marker for mercury-induced vascular damage: The modulatory effects of naringin
Autor: | Gamaleldin I. Harisa, Sabry M. Attiaa, Osama M. Abo-Salem, Amr D. Mariee |
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Rok vydání: | 2013 |
Předmět: |
chemistry.chemical_classification
Antioxidant biology Health Toxicology and Mutagenesis medicine.medical_treatment Glutathione peroxidase Glutathione reductase General Medicine Glutathione Management Monitoring Policy and Law Pharmacology Toxicology Nitric oxide Nitric oxide synthase chemistry.chemical_compound chemistry Biochemistry medicine TBARS biology.protein Nitrite |
Zdroj: | Environmental Toxicology. |
ISSN: | 1520-4081 |
DOI: | 10.1002/tox.21862 |
Popis: | In this study, endothelial nitric oxide synthase activity and nitric oxide (NO) production by human erythrocytes in the presence and absence of mercuric chloride (HgCl2 ), L-arginine (L-ARG), N ω- nitro-L-arginine methyl ester (L-NAME), and naringin (NAR) were investigated. In addition, the levels of reduced glutathione (GSH) and related enzymes were estimated in erythrocytes hemolysate. The protein carbonyl content (PCC) and thiobarbituric acid-reactive substances (TBARS) levels were also determined. The results of this study revealed that the treatment of erythrocytes with either HgCl2 or L-NAME induced a significant decrease in NOS activity and nitrite levels compared with control cells. Furthermore, mercury exposure significantly increased the levels of PCC and TBARS but reduced the GSH level. The activities of glucose-6-phosphate dehydrogenase, glutathione reductase, glutathione peroxidase, and glutathione-S-transferase (GST) were inhibited. The exposure of erythrocytes to HgCl2 in combination with L-ARG, NAR, or both ameliorated the investigated parameters compared with erythrocytes incubated with HgCl2 alone. These results indicate that mercury exposure decreased both erythrocyte NOS activity and nitrite production, and that these parameters might be indicative of mercury exposure. The data also suggest that concomitant treatment with NAR can restore NO bioavailability through either its metal-chelating properties or its antioxidant activity. |
Databáze: | OpenAIRE |
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