Why the study?
To examine the effects of a putative preferential mitochondrial reactive oxygen species scavenger in the brain of hypertensive transgenic (mRen2)27 rats.
Does ICV infusion of Mito-TEMPO or candesartan plus Ang-(1-7) improve blood pressure and sympathovagal balance in hypertensive (mRen2)27 rats?
Does ICV infusion of Mito-TEMPO or candesartan plus Ang-(1-7) improve blood pressure and sympathovagal balance in hypertensive (mRen2)27 rats?
In a rat model of chronic RAS-dependent hypertension, shifting the balance from Ang II toward Ang-(1-7) provides optimal therapeutic benefits for blood pressure and sympathovagal balance compared to mitochondrial ROS scavenging.
Hypertensive transgenic (mRen2)27 rats exhibit impaired baroreflex sensitivity (BRS) for control of heart rate (HR). Intracerebroventricular infusion of Ang-(1-7) improves indices of vagal BRS independent of lowering mean arterial pressure (MAP), whereas AT1 receptor blockade normalizes MAP and indices of sympathetic tone without correcting the vagal BRS. Scavenging cellular reactive oxygen species (ROS) with tempol in brain fails to correct either hypertension or sympathovagal balance in these animals, despite reports that mitochondrial ROS contributes to Ang II-infusion hypertension. To examine effects of a putative preferential mitochondrial ROS scavenger in the brain of (mRen2)27 rats, ICV infusions of Mito-TEMPO (3.2 μg/2.5 μL/h) were compared with artificial cerebrospinal fluid (aCSF; 2.5 μL/h) and combination AT1 receptor antagonist candesartan (CAN: 4 μg/2.5 μL/h) plus Ang-(1-7) (0.1 μg/2.5 μL/h) treatment. MAP was lower after CAN + Ang-(1-7) treatment, and both vagal and sympathetic components of BRS and sympathovagal balance were improved. By contrast, Mito-TEMPO improved sympathetic components of BRS and tended to improve overall sympathovagal balance but failed to alter MAP in this model of hypertension. Although further studies are required to determine whether Mito-TEMPO or CAN + Ang-(1-7) treatment at the doses used altered mitochondrial ROS, optimal therapeutic benefits are achieved by shifting the balance from Ang II toward Ang-(1-7) in this model of chronic RAS-dependent hypertension.
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Nautiyal et al. (2018) studied this question.
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