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Updated: Jun 3, 2026

Imaging Approaches to Assessments of Toxicological Oxidative Stress Using Genetically-encoded Fluorogenic Sensors
Published on: February 7, 2018
Urinary biomarkers of oxidative/nitrosative stress in healthy smokers
Carlos Campos1, Rodrigo Guzmán, Encarnación López-Fernández
1Department of Cellular and Molecular Medicine, Centre for Biological Research-Spanish National Research Council (CIB-CSIC), Madrid, Spain. ccampos@cib.csic.es
Objective:
To evaluate the effect of cigarette smoking on oxidative and nitrosative stress, we assessed urinary levels of 8-hydroxy-2'-deoxyguanosine (8-OHdG), isoprostane 15-F(2t)-IsoP, thiobarbituric acid-reacting substances (TBARS), advanced glycation end-products (AGEs), dityrosine (diTyr), hydrogen peroxide, total nitrite and nitrate and trolox equivalent antioxidant capacity (TEAC) in healthy smokers.
Methods:
Fluorimetric and spectrophotometric assays were performed in urine samples of 33 healthy smokers and 58 age-matched controls.
Results:
Levels of 8-OHdG, 15-F(2t)-IsoP and AGES were found significantly higher in smokers than in controls (10.7 ng/mg Cr vs. 8.3 ng/mg Cr, 1.41 ng/mg Cr vs. 1.01 ng/mg Cr and 189 AFU/mg Cr vs. 143 AFU/mg Cr, respectively; P < 0.05 for all). Positive correlations were found between age and levels of AGEs and diTyr in smokers (r = 0.380, P < 0.035 and r = 0.418, P < 0.019, respectively) and also between age and AGEs, diTyr and TEAC in controls (r = 0.474, P < 0.001, r = 0.463, P < 0.001 and r = 0.576, P < 0.001, respectively), being this correlation negative for 8-OHdG in controls (r = -0.295, P = 0.041). Positive correlation between the number of cigarettes smoked per day and AGEs was also found (r = 0.355, P = 0.044).
Conclusion:
Urinary 8-OHdG, 15-F(2t)-IsoP and AGEs may represent a non-invasive quantitative index of oxidant stress in healthy smokers, being AGEs a possible indicator of tobacco toxin exposure. The increased oxidative stress in healthy smokers observed may be generated because of an excessive production of reactive oxygen species and not by exhaustion of antioxidant defenses.
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