Treatment with escitalopram modulates cardiovascular function in rats

Considering depression is three times more common in cardiac patients compared to the normal population and selective serotonin reuptake inhibitors (SSRI) as drug of choice for treating patients with cardiovascular disease and depression, our work aims to evaluate the cardiovascular effects of treat...

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Veröffentlicht in:European journal of pharmacology 2018-04, Vol.824, p.120-127
Hauptverfasser: Veríssimo, Luiz Fernando, Volpini, Vinicius Lucca, Estrada, Viviane Batista, Matsubara, Natália Kimie, Gomes, Marcus Vinicius, Resstel, Leonardo Barbosa Moraes, Correa, Fernando Morgan Aguiar, Pelosi, Gislaine Garcia
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Sprache:eng
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Zusammenfassung:Considering depression is three times more common in cardiac patients compared to the normal population and selective serotonin reuptake inhibitors (SSRI) as drug of choice for treating patients with cardiovascular disease and depression, our work aims to evaluate the cardiovascular effects of treatment for 21 days with escitalopram (5 mg/kg/day, ip) in rats. The treatment caused an increase in mean arterial pressure concomitant with a decrease in heart rate. Concerning heart rate variability, there was a significant reduction in the sympathetic component and an elevation of the parasympathetic component, indicating that escitalopram caused an autonomic imbalance with parasympathetic predominance. In addition, we observed a decrease in both low and very low frequency power in blood pressure variability. The cardiac autonomic blockade indicated an increase in parasympathetic modulation to the heart with escitalopram chronic treatment. However, no change was observed on baroreflex activity. On the other hand, there was a decrease in pressure response during acute restraint stress with no changes in the tachycardia response. These findings showed that despite the escitalopram be a relatively safe drug it can cause tonic effects on cardiovascular function as well as during aversive situations.
ISSN:0014-2999
1879-0712
DOI:10.1016/j.ejphar.2018.02.003