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AT1R blocker prevents mental stress induced retrograde blood flow in overweight/obese men

The main goal was to determine the impact of mental stress (MS) on blood flow regulation in overweight/obese men. Fourteen overweight/obese men (27 ± 7 years; 29.8 ± 2.6 kg/m(2)) participated in two randomized experimental sessions with oral administration of the AT1R blocker Olmesartan (40 mg; AT1R...

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Detalles Bibliográficos
Autores principales: Rocha, Helena N. M., Teixeira, Gabriel F., Batista, Gabriel M. S., Storch, Amanda S., Garcia, Vinicius P., Mentzinger, Juliana, Gomes, Erika A. C., Campos, Monique O., Nóbrega, Antonio C. L., Rocha, Natália G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837474/
https://www.ncbi.nlm.nih.gov/pubmed/36636769
http://dx.doi.org/10.14814/phy2.15566
Descripción
Sumario:The main goal was to determine the impact of mental stress (MS) on blood flow regulation in overweight/obese men. Fourteen overweight/obese men (27 ± 7 years; 29.8 ± 2.6 kg/m(2)) participated in two randomized experimental sessions with oral administration of the AT1R blocker Olmesartan (40 mg; AT1RB) or placebo (PL). After 2 h, a 5‐min acute MS session (Stroop Color Word Test) was administered. Blood flow was assessed at baseline and during the first 3 min of MS by vascular ultrasound in the brachial artery. Blood was collected before (baseline) and during mental stress (MS) for measurement of nitrite (chemiluminescence) and endothelin‐1 (ELISA kit). The AT1R blocker was able to reverse the MS responses observed in the placebo session for retrograde flow (p < 0.01), retrograde SR (p < 0.01) and oscillatory shear index (p = 0.01). Regarding vasoactive substances, no differences were observed in ET‐1 (p > 0.05) responses to MS between experimental sessions. However, for nitrite responses, the administration of the AT1R blocker was able to increase circulating levels of NO (p = 0.03) Blockade of AT1R appears to prevent the decrease in endothelial function by reducing low shear stress and maintaining the vasoactive substances balance after MS in overweight/obese men.