z-logo
open-access-imgOpen Access
Interactive Effect of Ethnicity and ACE Insertion/Deletion Polymorphism on Vascular Reactivity
Author(s) -
James V. Gainer,
Christoph Stein,
Tami Neal,
Douglas E. Vaughan,
Nancy J. Brown
Publication year - 2001
Publication title -
hypertension
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.986
H-Index - 265
eISSN - 1524-4563
pISSN - 0194-911X
DOI - 10.1161/01.hyp.37.1.46
Subject(s) - bradykinin , sodium nitroprusside , medicine , endocrinology , vasodilation , angiotensin converting enzyme , endothelium , snp , blood pressure , genotype , chemistry , nitric oxide , single nucleotide polymorphism , gene , biochemistry , receptor
—Bradykinin is a potent endothelium-dependent vasodilator that contributes to the blood pressure lowering effect of angiotensin-converting enzyme inhibition. Angiotensin-converting enzyme inhibitors are widely prescribed for the treatment of hypertension, although the efficacy of this therapy has been reported to vary among different ethnic groups. To determine whether vascular sensitivity to bradykinin is decreased in blacks compared with whites, we measured forearm blood flow with venous plethysmography in response to intraarterially-administered bradykinin (100, 200, and 400 ng/min) under salt-controlled conditions in 28 (14 black, 14 white) normotensive subjects genotyped for theACE insertion/deletion (I/D ) polymorphism. Acetylcholine (ACh) (15, 30, and 60 μg/min) and sodium nitroprusside (SNP) (0.8, 1.6, and 3.2 μg/min) were infused as endothelium-dependent and endothelium-independent controls. Compared with whites, blacks exhibited a blunted vasodilator response to bradykinin (maximal blood flow: 20.4±2.5 versus 10.9±1.4 mL · 100 mL−1 · min−1 ,P =0.004) and SNP (14.1±1.6 versus 9.9±1.7 mL · 100 mL−1 · min−1 ,P =0.05) but not to ACh (10.5±2.8 versus 6.6±1.0 mL · 100 mL−1 · min−1 ,P =0.21). White subjects who carried at least 1ACE D allele demonstrated significantly greater vasodilator responses to bradykinin compared with those homozygous for theI allele (DD orID versusII , F=5.6,P <0.04). In contrast, only blacks homozygous for theACE D allele had a significantly greater vasodilator response to bradykinin than those who carried theI allele (DD versusID orII , F=8.3,P =0.01). The ethnic difference was most pronounced in subjects heterozygous at theACE I/D locus in which blacks had a markedly attenuated response to bradykinin compared with whites (F=41.0,P <0.001). There was no effect ofACE I/D genotype on the vasodilator responses to SNP or ACh in either ethnic group. These data confirm that vascular reactivity to bradykinin and the endothelium-independent vasodilator SNP is decreased in normotensive blacks compared with whites, consistent with attenuated vascular smooth muscle reactivity. The data suggest that genetic variation at theACE gene locus interacts with ethnicity to impact the vascular response to bradykinin.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom