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. 2021 Jun 30:2021:5569961.
doi: 10.1155/2021/5569961. eCollection 2021.

Alterations in the Plasma and Red Blood Cell Properties in Patients with Varicose Vein: A Pilot Study

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Alterations in the Plasma and Red Blood Cell Properties in Patients with Varicose Vein: A Pilot Study

Lukasz Gwozdzinski et al. Cardiol Res Pract. .

Abstract

The varicose vein results from the inefficient functioning of the valves in the lower limb veins, making the blood flow slow down and leading to blood stasis and hypoxia. This type of vein dysfunction might be a result of the development of oxidative stress. We compared oxidative stress markers in the plasma and erythrocytes obtained from peripheral veins and varicose veins in the same patients (glutathione, nonenzymatic antioxidant capacity (NEAC), catalase (CAT) and acetylcholinesterase (AChE) activity, thiols, thiobarbituric acid-reactive substance (TBARS), and protein carbonyls). We found a decrease in NEAC in the plasma obtained from the varicose veins compared to the peripheral veins. We detected a decrease in thiols in the plasma, hemolysate, and plasma membranes and increase in protein carbonyl compounds and TBARS levels in the varicose veins. These changes were accompanied by a decrease in CAT and AChE activity. For the first time, our results show changes in the plasma, erythrocyte membrane, and hemolysate protein properties in varicose vein blood in contrast to the plasma and erythrocytes in peripheral vein blood from the same patients. The increased oxidative stress accompanying varicose vein disease might result from the local inefficiency of the antioxidant defense system.

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Conflict of interest statement

The authors declare that they have no conflicts of interest.

Figures

Figure 1
Figure 1
The levels of free thiols (a), TBARS (b), and protein carbonyl compounds (c) in the plasma obtained from peripheral and varicose veins. Data are shown as mean ± range of standard deviation, n = 8. p < 0.05 is the significant difference.
Figure 2
Figure 2
Total nonenzymatic antioxidant capacity in the plasma, determined by (a) DPPH and (b) FRAP methods, and catalase activity (c) in the plasma of the blood samples obtained from peripheral and varicose veins. Data are presented as mean ± range of standard deviation, n = 8. p < 0.05 is the significant difference.
Figure 3
Figure 3
Mobility of ISL labeled hemoglobin (a), the levels of total thiols (b), and catalase activity (c) in the hemolysate obtained from a peripheral vein and a varicose vein. Data are shown as mean ± range of standard deviation, n = 8. p < 0.05 is the significant difference.
Figure 4
Figure 4
The levels of free thiols (a), protein carbonyl compounds (b), and acetylcholinesterase activity (c) in the erythrocyte membrane obtained from a peripheral vein and a varicose vein. Data are shown as mean ± range of standard deviation, n = 8. p < 0.05 is the significant difference.

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