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Effects of AT1 Receptor Blockade on Plasma Thromboxane A(2) (TXA(2)) Level and Skin Microcirculation in Young Healthy Women on Low Salt Diet

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posted on 2016-04-04, 00:00 authored by Ana Cavka, Anita Cosic, Ivana Grizelj, Akos Koller, Bojan Jelakovic, Julian H. Lombard, Shane A. Phillips, Ines Drenjancevic
Objective: To determine the effect of AT1 receptor antagonism on skin microcirculation and plasma level of thromboxane A2 (TXA2). Methods: Healthy women (n=20) maintained 7 days low salt (LS) diet (intake <40 mmol Na/day) without (LS) or together with 50 mg/per day of losartan (a selective AT1 receptor inhibitor) (LS diet+losartan group). Laser Doppler flowmetry (LDF) measurements of changes in post occlusive hyperemic blood flow, plasma concentration of stable TXA2 metabolite thromboxane B2 (TXB2) and plasma renin activity (PRA) aldosterone concentration, electrolytes (Na+, K+), as well as blood pressure and heart rate were determined before and after study protocols. Results: PRA and aldosterone increased significantly after 7 days of both LS diet and LS diet+losartan. LS diet or LS diet+losartan administrations had no significant effect on post-occlusion hyperemia While there was no change in TXB2 after LS diet TXB2 significantly increased after one week of LS+losartan compared to control levels (cTXB2 pg/mL control 101±80 vs. LS diet+losartan 190±116, p<0.05). Conclusion: These data suggest that inhibition of AT1 receptors could lead to activation of AT2 receptors, which maintain hyperemia, despite the increased level of vasoconstrictor TXA2. These findings also suggest an important role of crosstalk between renin-angiotensin system (RAS) and arachidonic acid metabolites in the regulation of microcirculation under physiological conditions.

Funding

This study was supported by a grant of the Ministry of Science, Education and Sports of the Republic of Croatia: Effects of oxygen on vascular function in health and disease #219-2160133-2034, SROP-4.2.2.A-11/1/KONV-2012-0024 and Hungarian Natl Sci Res Fund (OTKA) K 108444.

History

Publisher

Royal Society of Chemistry

Language

  • en_US

issn

1420-4096

Issue date

2013-01-01

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