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[THE ANTIOXIDANT EFFECT OF DALARGIN IN PATIENTS WITH CORONARY HEART DISEASE AND METABOLIC SYNDROME]
Insights
Dalargin supplementation significantly reduced oxidative stress and improved antioxidant capacity in patients with coronary heart disease and metabolic syndrome. Standard therapy alone showed no significant changes in these markers.
Area of Science:
- Cardiology
- Biochemistry
- Pharmacology
Background:
- Coronary heart disease (CHD) and metabolic syndrome (MS) are associated with increased oxidative stress.
- Lipid peroxidation (LPO) and an imbalanced antioxidant system are key factors in cardiovascular disease progression.
Purpose of the Study:
- To investigate the impact of dalargin on lipid peroxidation and the antioxidant system in patients with CHD and MS.
- To compare the effects of standard therapy (ST) versus ST plus dalargin (ST + D) on oxidative stress markers.
Main Methods:
- A study involving 123 patients with stable CHD and MS.
- Comparison of blood redox potential (EP), total antioxidant activity (TAA), oxidized low-density lipoproteins (LDL), and superoxide dismutase (SOD) activity.
- Patients received either ST or ST + D (1 mg intranasally twice daily for 10 days, repeated for 3 months).
Main Results:
- Standard therapy alone did not yield significant changes in EP, oxidized LDL, or SOD activity over 3 months.
- The addition of dalargin (ST + D) significantly decreased oxidative stress markers: blood EP by 10.5% and oxidized LDL by 14% (p < 0.001).
- Dalargin significantly enhanced antioxidant properties: SOD activity increased by 36.1% and TAA by 25.3% (p < 0.001).
Conclusions:
- Dalargin demonstrates a significant therapeutic effect in mitigating oxidative stress in patients with CHD and MS.
- Supplementing standard therapy with dalargin effectively improves the antioxidant system, offering a potential new treatment avenue.
Abstract:
The aim of this study was to evaluate the effect of dalargin on the state of lipid peroxidation (LPO) and antioxidant system in patients with coronary heart disease (CHD) and on the background of metabolic syndrome (MS) in a group of 123 patients with stable coronary artery disease and MS (mean age 56.7 ± 5.1 years). For this purpose, the blood redox potential (EP), total antioxidant activity (TAA), level of oxidized low density lipoproteins (LDL), and activity of superoxide dismutase (SOD) were compared between the group receiving a standard medical therapy (ST) for coronary heart disease (group 1, n = 63) and that with supplementary dalargin administration (ST + D) in a dose of 1 mg intranasally twice a day for 10 days (group 2, n = 60), using the same dose for 10 days in the next two months (total 3 courses over 3 months). It was found that patients with CHD + MS upon 3-month ST showed no statistically significant changes in parameters characterizing the oxidative potential of blood (EP) and antioxidant protection of blood (oxidized LDL level, SOD activity). The inclusion of dalargin into therapy (ST + D) led to a significant decrease in the oxidative stress parameters (blood EP by 10.5%, oxidized LDL level by 14%, p < 0.001) and increase in the blood antioxidant properties (SOD activity by 36.1%, TAA by 25.3%, p < 0.001).
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