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Glutathione-related antioxidant defense system in elderly patients treated for hypertension
J Rybka1, D Kupczyk, K Kędziora-Kornatowska
1Department of Biochemistry, Nicolaus Copernicus University in Toruń, L. Rydygier Collegium Medicum in Bydgoszcz, Poland. joanna.rybka1@wp.pl
Insights
Elderly hypertensive patients on medication show enhanced glutathione antioxidant defense, including higher glutathione (GSH) levels and glutathione reductase (GR) activity. This suggests a role for the glutathione system in blood pressure regulation and treatment effects.
Area of Science:
- Biochemistry
- Gerontology
- Cardiovascular Medicine
Background:
- Hypertension is a prevalent condition in the elderly.
- Oxidative stress plays a role in hypertension.
- The glutathione system is a key endogenous antioxidant defense mechanism.
Purpose of the Study:
- To investigate the glutathione antioxidant defense system in elderly patients with hypertension undergoing treatment.
- To compare glutathione levels and enzyme activities between hypertensive patients and healthy controls.
Main Methods:
- Blood samples were collected from 18 hypertensive patients (over 60) on medication and 15 age/sex-matched controls.
- Whole blood glutathione (GSH) concentration was measured.
- Erythrocyte glutathione peroxidase (GPx-1), glutathione transferase (GST), and glutathione reductase (GR) activities were assessed.
- Statistical analysis was performed using independent-samples t test.
Main Results:
- Elderly hypertensive patients exhibited significantly higher mean GSH concentration (3.1 ± 0.29 mmol/L vs. 2.6 ± 0.25 mmol/L, P < 0.001).
- Mean GR activity was significantly elevated in hypertensives (83.4 ± 15.25 U/g Hb vs. 64.2 ± 8.26 U/g Hb, P < 0.001).
- Mean GST activity was also significantly higher in the hypertensive group (3.0 ± 0.60 mmol CDNB-GSH/mgHb/min vs. 2.6 ± 0.36 mmol CDNB-GSH/mgHb/min, P < 0.05).
- No significant difference in GPx activity was found between groups.
Conclusions:
- The glutathione antioxidant defense system is enhanced in elderly hypertensive patients receiving antihypertensive treatment.
- This finding suggests a potential role for the glutathione system in blood pressure regulation.
- Observed alterations in antioxidant status may be linked to the impact of antihypertensive medications on nitric oxide bioavailability.
Abstract:
The purpose of this study was to analyze glutathione antioxidant defense system in elderly patients treated for hypertension. Studies were carried out in the blood collected from 18 hypertensive and 15 age- and sex-matched controls, all subjects age over 60. Hypertensives were on their usual antihypertensive treatment at the time of blood collection. The concentration of glutathione (GSH) in whole blood and activities of glutathione peroxidase (GPx-1), glutathione transferase (GST), and glutathione reductase (GR) in erythrocytes were measured. The data from patients and controls were compared using independent-samples t test. P value of 0.05 and less was considered statistically significant. We observed increased glutathione-related antioxidant defense in treated hypertensive elderly patients (HT) when compared with healthy controls (C). Mean GSH concentration was significantly higher in HT when compared with C: 3.1 ± 0.29 and 2.6 ± 0.25 mmol/L, respectively, P < 0.001. Mean activity of GR was significantly higher in HT group if compared with C: 83.4 ± 15.25 U/g Hb versus 64.2 ± 8.26 U/g Hb, respectively, P < 0.001. Mean activity of GST was significantly higher in HT group compared with C: 3.0 ± 0.60 mmol CDNB-GSH/mgHb/min and 2.6 ± 0.36 mmol CDNB-GSH/mgHb/min, respectively, P < 0.05. No difference in GPx activity was observed between two groups. These results show that glutathione-related antioxidant defense system was enhanced in elderly hypertensive patients treated for their conditions. This suggests important role of glutathione system in blood pressure regulation. Alterations in concentration and activity of antioxidants observed during antihypertensive medication are likely to be related to the effect of the treatment on NO bioavailability.
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