Apocynin but Not-L-Arginine Prevents and Reverses Dexamethasone-Induced Hypertension in the Rat
Loading...
Date
Authors
Hu, Lexian
Zhang, Yi
Lim, Pek (Chloe)
Miao, Yuchun
Tan, Chrismin
McKenzie, Katja
Schyvens, Chris
Whitworth, Judith
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
Abstract
Background: Dexamethasone (Dex)-hypertension in rats is associated with increased oxidative stress. We investigated effects of the NAD(P)H oxidase inhibitor apocynin and the nitric oxide (NO) precursor l-arginine on Dex-hypertension to determine the relative roles of NAD(P)H oxidase and uncoupling in the reactive oxygen species (ROS) generation and hypertension. Methods: Male Sprague-Dawley rats (n = 10/group) received Dex (20 μg/kg/day subcutaneously) or saline (vehicle) for 14 days. In a prevention study, rats received 4 days of apocynin treatement (1.5 mmol/L in drinking water) followed by Dex/saline for 12 days. In reversal studies, apocynin or l-arginine was given from day 8 to 14. Systolic blood pressure (SBP) was measured by tail cuff, and thymus weight was used as a marker of glucocorticoid activity. Results: Administration of Dex increased SBP (104 ± 3 to 122 ± 3 mm Hg, P < .01, mean ± SEM) and decreased thymus and body weight (P′ < .05). Apocynin alone had no effect on SBP, BW, or thymus weight. Apocynin prevented (122 ± 4 Dex, 111 ± 3 mm Hg Apocynin+Dex, P′ < .05) and reversed Dex-hypertension (130 ± 4 to 116 ± 4 mm Hg, P < .01). L-arginine did not reverse Dex-hypertension. Conclusions: In male SD rats, apocynin but not l-arginine prevented and reversed Dex-hypertension, suggesting that NAD(P)H oxidase-mediated superoxide production but not endothelial nitric oxide synthase uncoupling is important in Dex-hypertension.
Description
Citation
Collections
Source
American Journal of Hypertension
Type
Book Title
Entity type
Access Statement
License Rights
Restricted until
2037-12-31
Downloads
File
Description