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Ultrasound Assessment of Endothelial Function: A Technical Guideline of the Flow-mediated Dilation Test
Published on: April 27, 2016
Effect of carvedilol and nebivolol on oxidative stress-related parameters and endothelial function in patients with
Ramiro J Zepeda1, Rodrigo Castillo, Ramón Rodrigo
1Molecular and Clinical Pharmacology Program, Faculty of Medicine, Biomedical Sciences Institute, Universidad de Chile, Santiago, Chile. rzepeda@ciq.uchile.cl
Insights
This study found both carvedilol and nebivolol effectively lower blood pressure in essential hypertension (EH) patients. Carvedilol improved antioxidant capacity, while nebivolol increased nitric oxide (NO₂) levels, suggesting different mechanisms for their antihypertensive effects.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Biochemistry
Background:
- Essential hypertension (EH) is linked to oxidative stress and endothelial dysfunction.
- Understanding the mechanisms of antihypertensive drugs is crucial for effective treatment.
Purpose of the Study:
- To compare the effects of carvedilol and nebivolol on oxidative stress markers and endothelial function in patients with EH.
- To investigate the distinct mechanisms by which these beta-blockers exert their antihypertensive effects.
Main Methods:
- A randomized study involving 57 mild-to-moderate EH patients (30-75 years).
- Participants received either carvedilol (12.5 mg) or nebivolol (5 mg) for 12 weeks.
- Evaluated 24-hour ambulatory blood pressure, flow-mediated dilatation, plasma nitrite (NO₂), and oxidative stress markers.
Main Results:
- Both drugs significantly reduced systolic and diastolic blood pressure compared to baseline.
- Nebivolol and carvedilol improved endothelium-dependent dilatation by 7.3% and 8.1%, respectively.
- Carvedilol increased plasma antioxidant capacity (FRAP, GSSH/GSH ratio), while nebivolol significantly elevated plasma nitrite (NO₂) levels.
Conclusions:
- Both carvedilol and nebivolol demonstrate significant antihypertensive effects in EH patients.
- Carvedilol may exert its effects through enhanced antioxidant capacity.
- Nebivolol appears to improve endothelial function and lower blood pressure by increasing nitric oxide bioavailability.
Abstract:
Oxidative stress and endothelial dysfunction have been associated with essential hypertension (EH) mechanisms. The purpose of this study was to evaluate the effect of carvedilol and nebivolol on the oxidative stress-related parameters and endothelial function in patients with EH. The studied population included 57 patients, either sex, between 30 and 75 years of age, with mild-to-moderate EH complications. Participants were randomized to receive either carvedilol (12.5 mg) (n = 23) or nebivolol (5 mg) (n = 21) for 12 weeks. Measurements included; 24-hr ambulatory blood pressure (BP), flow-mediated dilatation, levels of nitric oxide estimated as nitrite - a nitric oxide metabolite ( NO₂) - in plasma, and oxidative stress-related parameters in plasma and erythrocyte. EH patients who were treated with nebivolol or carvedilol showed systolic BP reductions of 17.4 and 19.9 mmHg, respectively, compared with baseline values (p < 0.01). Diastolic BP was reduced by 13.7 and 12.8 mmHg after the treatment with ebivolol and carvedilol, respectively (p < 0.01) (fig. 2B). Nebivolol and carvedilol showed 7.3% and 8.1% higher endothelium-dependent dilatation in relation to baseline values (p < 0.05). Ferric-reducing ability of plasma (FRAP) and reduced glutathione/oxidized glutathione (GSSH) ratio showed 31.5% and 29.6% higher levels in the carvedilol group compared with basal values; however, nebivolol-treated patients did not show significant differences after treatment. On the other hand, the NO₂ plasma concentration was not modified by the administration of carvedilol. However, nebivolol enhanced these levels in 62.1% after the treatment. In conclusion, this study demonstrated the antihypertensive effect of both beta-blockers. However, carvedilol could mediate these effects by an increase in antioxidant capacity and nebivolol through the raise in NO₂ concentration. Further studies are needed to determine the molecular mechanism of these effects.
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