Aldosterone receptor antagonism normalizes vascular function in liquorice-induced hypertension - PubMed (original) (raw)
Comparative Study
. 2001 Feb;37(2 Pt 2):801-5.
doi: 10.1161/01.hyp.37.2.801.
Affiliations
- PMID: 11230376
- DOI: 10.1161/01.hyp.37.2.801
Comparative Study
Aldosterone receptor antagonism normalizes vascular function in liquorice-induced hypertension
T Quaschning et al. Hypertension. 2001 Feb.
Abstract
The enzyme 11beta-hydroxysteroid dehydrogenase (11beta-HSD2) provides mineralocorticoid receptor specificity for aldosterone by metabolizing glucocorticoids to their receptor-inactive 11-dehydro derivatives. The present study investigated the effects of the aldosterone receptor antagonists spironolactone and eplerenone on endothelial function in liquorice-induced hypertension. Glycyrrhizic acid (GA), a recognized inhibitor of 11beta-HSD2, was supplemented to the drinking water (3 g/L) of Wistar-Kyoto rats over a period of 21 days. From days 8 to 21, spironolactone (5.8+/-0.6 mg. kg(-1). d(-1)), eplerenone (182+/-13 mg. kg(-1). d(-1)), or placebo was added to the chow (n=7 animals per group). Endothelium-dependent or -independent vascular function was assessed as the relaxation of preconstricted aortic rings to acetylcholine or sodium nitroprusside, respectively. In addition, aortic endothelial nitric oxide synthase (eNOS) protein content, nitrate tissue levels, and endothelin-1 (ET-1) protein levels were determined. GA increased systolic blood pressure from 142+/-8 to 185+/-9 mm Hg (P<0.01). In the GA group, endothelium-dependent relaxation was impaired compared with that in controls (73+/-6% versus 99+/-5%), whereas endothelium-independent relaxation remained unchanged. In the aortas of 11beta-HSD2-deficient rats, eNOS protein content and nitrate tissue levels decreased (1114+/-128 versus 518+/-77 microgram/g protein, P<0.05). In contrast, aortic ET-1 protein levels were enhanced by GA (308+/-38 versus 497+/-47 pg/mg tissue, P<0.05). Both spironolactone and eplerenone normalized blood pressure in animals on GA (142+/-9 and 143+/-9 mm Hg, respectively, versus 189+/-8 mm Hg in the placebo group; P<0.01), restored endothelium-dependent relaxation (96+/-3% and 97+/-3%, respectively, P<0.01 versus placebo), blunted the decrease in vascular eNOS protein content and nitrate tissue levels, and normalized vascular ET-1 levels. This is the first study to demonstrate that aldosterone receptor antagonism normalizes blood pressure, prevents upregulation of vascular ET-1, restores NO-mediated endothelial dysfunction, and thus, may advance as a novel and specific therapeutic approach in 11beta-HSD2-deficient hypertension.
Similar articles
- Endothelin 1 type a receptor antagonism prevents vascular dysfunction and hypertension induced by 11beta-hydroxysteroid dehydrogenase inhibition: role of nitric oxide.
Ruschitzka F, Quaschning T, Noll G, deGottardi A, Rossier MF, Enseleit F, Hürlimann D, Lüscher TF, Shaw SG. Ruschitzka F, et al. Circulation. 2001 Jun 26;103(25):3129-35. doi: 10.1161/01.cir.103.25.3129. Circulation. 2001. PMID: 11425780 - Influence of aldosterone vs. endothelin receptor antagonism on renovascular function in liquorice-induced hypertension.
Quaschning T, Ruschitzka F, Niggli B, Lunt CM, Shaw S, Christ M, Wehling M, Lüscher TF. Quaschning T, et al. Nephrol Dial Transplant. 2001 Nov;16(11):2146-51. doi: 10.1093/ndt/16.11.2146. Nephrol Dial Transplant. 2001. PMID: 11682659 - Addition of the selective aldosterone receptor antagonist eplerenone to ACE inhibition in heart failure: effect on endothelial dysfunction.
Schäfer A, Fraccarollo D, Hildemann SK, Tas P, Ertl G, Bauersachs J. Schäfer A, et al. Cardiovasc Res. 2003 Jun 1;58(3):655-62. doi: 10.1016/s0008-6363(03)00333-x. Cardiovasc Res. 2003. PMID: 12798439 - Glucocorticoid-mediated mineralocorticoid receptor activation and hypertension.
Frey FJ, Odermatt A, Frey BM. Frey FJ, et al. Curr Opin Nephrol Hypertens. 2004 Jul;13(4):451-8. doi: 10.1097/01.mnh.0000133976.32559.b0. Curr Opin Nephrol Hypertens. 2004. PMID: 15199296 Review. - Eplerenone: a selective aldosterone receptor antagonist for hypertension and heart failure.
Moore TD, Nawarskas JJ, Anderson JR. Moore TD, et al. Heart Dis. 2003 Sep-Oct;5(5):354-63. doi: 10.1097/01.hdx.0000089783.30450.cb. Heart Dis. 2003. PMID: 14503934 Review.
Cited by
- Blockade of the mineralocorticoid receptor improves markers of human endothelial cell dysfunction and hematological indices in a mouse model of sickle cell disease.
Rivera A, Vega C, Ramos-Rivera A, Maldonado ER, Prado GN, Karnes HE, Fesko YA, Snyder LM, Alper SL, Romero JR. Rivera A, et al. FASEB J. 2023 Aug;37(8):e23092. doi: 10.1096/fj.202300671R. FASEB J. 2023. PMID: 37482902 Free PMC article. Clinical Trial. - Clinical Risk Factors of Licorice-Induced Pseudoaldosteronism Based on Glycyrrhizin-Metabolite Concentrations: A Narrative Review.
Yoshino T, Shimada S, Homma M, Makino T, Mimura M, Watanabe K. Yoshino T, et al. Front Nutr. 2021 Sep 17;8:719197. doi: 10.3389/fnut.2021.719197. eCollection 2021. Front Nutr. 2021. PMID: 34604277 Free PMC article. Review. - Decreased 11β-Hydroxysteroid Dehydrogenase Type 2 Expression in the Kidney May Contribute to Nicotine/Smoking-Induced Blood Pressure Elevation in Mice.
Wang Y, Wang J, Yang R, Wang P, Porche R, Kim S, Lutfy K, Liu L, Friedman TC, Jiang M, Liu Y. Wang Y, et al. Hypertension. 2021 Jun;77(6):1940-1952. doi: 10.1161/HYPERTENSIONAHA.120.16458. Epub 2021 Apr 5. Hypertension. 2021. PMID: 33813843 Free PMC article. - Liquorice ingestion attenuates vasodilatation via exogenous nitric oxide donor but not via β2-adrenoceptor stimulation.
Hautaniemi EJ, Tikkakoski AJ, Eräranta A, Kähönen M, Hämäläinen E, Turpeinen U, Huhtala H, Mustonen J, Pörsti IH. Hautaniemi EJ, et al. PLoS One. 2019 Oct 18;14(10):e0223654. doi: 10.1371/journal.pone.0223654. eCollection 2019. PLoS One. 2019. PMID: 31626649 Free PMC article. - Bioactive Candy: Effects of Licorice on the Cardiovascular System.
Deutch MR, Grimm D, Wehland M, Infanger M, Krüger M. Deutch MR, et al. Foods. 2019 Oct 14;8(10):495. doi: 10.3390/foods8100495. Foods. 2019. PMID: 31615045 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical