Journal Article

Antihypertensive effect of etamicastat in dopamine D2 receptor-deficient mice

Serrão, Maria Paula, Jones, John E., Cuevas, Santiago, Grandy, David K., Asico, Laureano D., Armando, Ines, Wang, Xiaoyan, Soares-da-Silva, Patricio, Jose, Pedro A.

2018

Overview

Abnormalities of the D R gene (DRD2) play a role in the pathogenesis of human essential hypertension; variants of the DRD2 have been reported to be associated with hypertension. Disruption of Drd2 (D ) in mice increases blood pressure. The hypertension of D mice has been related, in part, to increased sympathetic activity, renal oxidative stress, and renal endothelin B receptor (ETBR) expression. We tested in D mice the effect of etamicastat, a reversible peripheral inhibitor of dopamine-β-hydroxylase that reduces the biosynthesis of norepinephrine from dopamine and decreases sympathetic nerve activity. Blood pressure was measured in anesthetized D mice treated with etamicastat by gavage, (10 mg/kg), conscious D mice, and D littermates, and mice with the D R selectively silenced in the kidney, treated with etamicastat in the drinking water (10 mg/kg per day). Tissue and urinary catecholamines and renal expression of selected G protein-coupled receptors, enzymes related to the production of reactive oxygen species, and sodium transporters were also measured. Etamicastat decreased blood pressure both in anesthetized and conscious D mice and mice with renal-selective silencing of D R to levels similar or close to those measured in D littermates. Etamicastat decreased cardiac and renal norepinephrine and increased cardiac and urinary dopamine levels in D mice. It also normalized the increased renal protein expressions of ETBR, NADPH oxidase isoenzymes, and urinary 8-isoprostane, as well as renal NHE3 and NCC, and increased the renal expression of D R but not D R in D mice. In conclusion, etamicastat is effective in normalizing the increased blood pressure and some of the abnormal renal biochemical alterations of D mice.

• Publisher: Nature Publishing Group
• Subject: Antihypertensives / Blood pressure / Dopamine / Hypertension / Reactive oxygen species